A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Gene Dmel\dlg1

General Information
SymbolDmel\dlg1SpeciesD. melanogaster
Namediscs large 1Annotation symbolCG1725
Feature typeprotein_coding_geneFlyBase IDFBgn0001624
Gene Model StatusCurrent Stock availability 32 publicly available
Also Known Asdlg, DlgA, l(1)d.lg-1, Dlg-A, misb, dlg-1, l(1)dlg, l(1)dlg-1, l(1)discs large, l(1)bwn
Genomic Location
Chromosome (arm)XRecombination map1-34.8
Cytogenetic map10B6-10B10Sequence locationX:11,263,670..11,303,320 [+]

Genomic Maps

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modENCODE GBrowse
detailed view
hide Summary Information
Automatically generated summary

See sections below for more information
The gene discs large 1 is referred to in FlyBase by the symbol Dmel\dlg1 (CG1725, FBgn0001624). It is a protein_coding_gene from Drosophila melanogaster. There is experimental evidence that it has the molecular function: protein binding. There is experimental evidence for 16 unique biological process terms, many of which group under: anatomical structure development; localization; cellular component organization or biogenesis; macromolecule localization; mating; protein localization; morphogenesis of follicular epithelium; behavioral interaction between organisms; multicellular organismal reproductive process; synaptic transmission; locomotory behavior; establishment or maintenance of polarity of follicular epithelium; locomotion. 99 alleles are reported. The phenotypes of these alleles are annotated with: organ system subdivision; nervous system; organ system; multi-cell-component structure; adult segment; presumptive embryonic/larval nervous system; imaginal precursor; female germline cyst; plasma membrane part; cuticle. It has 17 annotated transcripts and 17 annotated polypeptides. Protein features are: Guanylate kinase; Guanylate kinase, conserved site; Guanylate kinase/L-type calcium channel; L27; L27-1; PDZ/DHR/GLGF; Src homology-3 domain; Variant SH3. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of moderately high expression to a trough of moderate expression. Peak expression observed at stages throughout embryogenesis, during early larval stages, during late pupal stages, in stages of adults of both sexes. Summary of FlyAtlas Anatomical Expression Data: Two or more Affy2 ProbeSets identify exons of this gene. This is a summary of the tissue expression peaks exhibited in at least one of these ProbeSets. Expression in all larval and adult organs/tissues ranges from low to undetected. Expression at high levels in the following post-embryonic organs or tissues: adult eye. Expression at moderate levels in the following post-embryonic organs or tissues: adult head, larval/adult central nervous system, adult crop, larval/adult hindgut, adult heart, adult fat body, larval/adult salivary gland, larval trachea, adult ovary, adult male accessory gland, larval/adult carcass. Gene sequence location is X:11263670..11303320.

External Summaries
hide Phenotypic Description from the Red Book (Lindsley & Zimm 1992)
Gene/Allele symbols may differ from current usage
dlg1: discs large
Late larval lethal; prolonged larval stages with bloated larvae attempting pupariation around day 15; some cuticular tanning, but no adult cuticular structures formed. During early larval development, the imaginal discs are smaller than those of normal larvae of the same age and are misshapen, but as the larvae continue to survive after the normal pupariation time, the discs continue to grow. They become large, amorphous, and solid, containing three times the normal numbers of cells at ten days of age; they also experience substantial cell death. By eleven days, wing and haltere discs may fuse; also first and second leg discs fuse with ventral ganglion of the CNS; great enlargement of optic lobes of brain also takes place. Discs, but not brains, transplanted into adults grow rapidly displaying invasive growth; they do not differentiate when transplanted into larvae for metamorphosis. Homozygous tissues do not survive, nor do gynandromorphs (one with male abdominal tissue vs. 66 expected). It is possible to produce homozygous germ-line clones (Perrimon). dlg1 embryos generated from such clones display defects in morphogenesis and neurogenesis; most tissues are defective; partial rescue achieved by a paternal dlg1+ contribution, in the form of either a normal X or a v+Y.
dlg12
Homozygotes fail to survive when raised at 25; when raised at 18 however, 37% survival attained; hemizygous females show 65-70% survival at 18, but are also lethal at 25. Survival at 18 nearly complete in heterozygotes with dlg15 and dlg118, and survival at 25 is 4% and 95% respectively. Embryos produced by matings between surviving dlg12 flies raised at 18 show but 4% hatchability at 18, and such crosses are completely sterile at 25; however in crosses of homozygous dlg1+2 females to dlg1+ males, rescue of heterozygous daughters nearly complete at either 18 or 25 and is somewhat reduced at 29. Abnormal embryos produced by dlg12 females show failure of dorsal closure, and head involution. The maternal effect of dlg1 is germ-line specific, since embryos produced by homozygous clones in heterozygous mothers are indistinguishable from those produced by homozygous mothers (Perrimon, 1988, Dev. Biol. 127: 392-407).
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Description
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What does this section not display?
This section does not currently display links that were removed or gene model changes.
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FB2012_01
Sequence features
Controlled Vocabulary Terms
References
FB2011_10
References
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Detailed Mapping Data
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
10B6-10B10  
Limits computationally determined from genome sequence between P{EP}CG11756EP1610 and P{EP}CG32666EP1452  
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
10B14-10B17  
(determined by in situ hybridisation) 10B8--11 (determined by in situ hybridisation)  
10B8-10B11  
(determined by in situ hybridisation)  
10B8-10B11  
(determined by in situ hybridisation)  
10B14-10B17  
(determined by in situ hybridisation)  
10B8-10B11  
(determined by in situ hybridisation)  
Experimentally Determined Recombination Data
Location
1-34.8
 
Left of (cM)
Right of (cM)
Notes
hide Gene Model & Products
Please see the GBrowse view of Dmel\dlg1 for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
detailed view FBtr0073457 FBtr0073482 FBtr0073490 FBtr0073491 FBtr0073492 FBtr0073483 FBtr0112813 FBtr0073488 FBtr0302114 FBtr0073484 FBtr0301288 FBtr0112812 FBtr0073487 FBtr0308089 FBtr0073489 FBtr0073485 FBtr0301289 FBtr0073486 FBtr0308088 FBtr0300849 FBtr0309222 FBpp0073338 FBpp0089351 FBpp0089349 FBpp0111725 FBpp0073339 FBpp0089353 FBpp0291324 FBpp0089348 FBpp0290503 FBpp0073340 FBpp0111724 FBpp0300431 FBpp0300432 FBpp0290504 FBpp0089350 FBpp0073342 FBpp0073341 FBpp0089352 FBpp0301161 FBpp0290073 FBti0071723 FBti0024932 FBti0052587 FBti0068320 FBti0037321 FBti0057169 FBti0056717 FBti0144076 FBti0048400 FBti0035750 FBti0014401 FBti0027353 FBti0029819 FBti0071354 FBti0034181 FBti0145080 FBti0028565 FBti0013927 FBti0051544 FBti0015516 FBti0099888 FBti0143657 FBti0038104 FBti0053764 FBti0143790 FBti0042857
Comments on Gene Model
Gene model reviewed during 5.40
Gene model includes transcripts encoding non-overlapping portions of the full CDS.
hide Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Associated CDS (aa)
FBtr0073486
  4864
  968
FBtr0073488
  5324
  970
FBtr0073483
  2582
  208
FBtr0073485
  4822
  960
FBtr0073487
  4707
  960
FBtr0073484
  2554
  816
FBtr0073489
  4867
  975
FBtr0073490
  5147
  911
FBtr0073491
  2142
  208
FBtr0073492
  2130
  208
FBtr0112812
  6065
  911
FBtr0112813
  6788
  946
FBtr0301288
  3196
  1030
FBtr0301289
  4840
  960
FBtr0302114
  2361
  206
FBtr0308088
 
  4841
  983
FBtr0308089
 
  5336
  975
Additional Transcript Data & Comments
Reported size (kB)
5.1 (longest cDNA)
Comments
External Data
Crossreferences
hide Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
RefSeq ID
GenBank protein
FBpp0073342  
103.2  
968  
8.49  
FBpp0089351  
106.7  
970  
6.75  
FBpp0073339  
24.4  
208  
10.43  
FBpp0073341  
102.4  
960  
7.87  
FBpp0089350  
102.4  
960  
7.87  
FBpp0073340  
88.7  
816  
4.49  
FBpp0089352  
104.0  
975  
7.15  
FBpp0089353  
100.2  
911  
6.95  
FBpp0089348  
24.4  
208  
10.43  
FBpp0089349  
24.4  
208  
10.43  
FBpp0111724  
100.5  
911  
8.77  
FBpp0111725  
104.3  
946  
6.61  
FBpp0290503  
112.5  
1030  
4.80  
FBpp0290504  
102.4  
960  
7.87  
FBpp0291324  
24.2  
206  
10.43  
FBpp0300431  
104.9  
983  
7.56  
 
 
FBpp0300432  
104.0  
975  
7.15  
 
 
Additional Polypeptide Data & Comments
Reported size (kDa)
960 (aa); 102 (kD)
Comments
External Data
Linkouts
Crossreferences
InterPro domains - A database of protein families, domains, and functional sites
PDZ/DHR/GLGF (IPR001478)
L27 (IPR004172)
Guanylate kinase (IPR008144)
L27-1 (IPR015143)
Variant SH3 (IPR011511)
hide Sequences Consistent with the Gene Model
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
hide Mapped Features
Mapped Features have been reorganized, please see this article for details.
Additional mapped features and mutations can be found on GBrowse or related reports.
Type
Symbol & Location
Additional Notes
References
hide External Data
Linkouts
Crossreferences
hide Expression Data
hideTranscript Expression
in situ
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data
dlg1 transcripts are expressed throughout development.
Marker for
Subcellular Localization
CV Term
Notes
hidePolypeptide Expression
immunolocalization
Stage
Tissue/Position (including subcellular localization)
Reference
mass spectroscopy
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data
dlg1 protein is found mainly in epithelia, where it is localized at the apical part of the lateral cell membrane.
dlg1 is expressed in central brain neuropils. Lamina cross-sections exhibited a bright ring of R1-R6 terminals that label with dlg1. Using immunoelectron microscopy, dlg1 is often seen close to the heads of the capitate projections (invaginations from surrounding epithelial glial and specialised organelles for the endocytosis of vesicle membrane), but not the stalks.
Expression of dlg1 is observed in the neuromuscular junction of wildtype fly at 3, 15, 30 and 60 days post-eclosion.
Marker for
Subcellular Localization
CV Term
septate junction
Notes
hide High-Throughput Expression Data
or
Untitled Document detailed view Tim8-RA dlg1-RH dlg1-RI dlg1-RJ dlg1-RC dlg1-RL dlg1-RB dlg1-RO dlg1-RF dlg1-RM dlg1-RK dlg1-RE dlg1-RQ dlg1-RG dlg1-RD dlg1-RN dlg1-RA dlg1-RP CG15196-RB CG15196-RC
See Gelbart and Emmert, 2010.10.13 for analysis details and data files for all genes.

modENCODE Temporal Expression Data for FBgn0001624


   Styles
Linear
Logarithmic
Heatmap
   Scales
max expr for FBgn0001624
Very low expression bin max
Moderate expression bin max
High expression bin max
Extremely high expression bin max

Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of moderately high expression to a trough of moderate expression. Peak expression observed at stages throughout embryogenesis, during early larval stages, during late pupal stages, in stages of adults of both sexes.
[download data (TSV)]

Guide to modENCODE expression level colors
 
No expression (0 - 0)
 
Extremely low expression (1 - 10)
 
Very low expression (11 - 100)
 
Low expression (101 - 400)
 
Moderate expression (401 - 1400)
 
Moderately high expression (1401 - 4000)
 
High expression (4001 - 10000)
 
Very high expression (10001 - 100000)
 
Extremely high expression (100001 - 2000000)

Linear, scaled to maximum FBgn0001624 expression level
Developmental Stage   Expression Level
embryo 00-02hr
 
 1687
embryo 02-04hr
 
 3145
embryo 04-06hr
 
 3190
embryo 06-08hr
 
 2434
embryo 08-10hr
 
 2296
embryo 10-12hr
 
 1605
embryo 12-14hr
 
 1878
embryo 14-16hr
 
 2105
embryo 16-18hr
 
 2557
embryo 18-20hr
 
 2374
embryo 20-22hr
 
 2405
embryo 22-24hr
 
 2288
larva L1
 
 1630
larva L2
 
 1124
larva L3 12hr old
 
 1145
larva L3 puffstage 1-2
 
 553
larva L3 puffstage 3-6
 
 1005
larva L3 puffstage 7-9
 
 1064
white prepupae new
 
 1074
white prepupae 12hr
 
 957
white prepupae 24hr
 
 1323
pupae 2d postWPP
 
 1627
pupae 3d postWPP
 
 2783
pupae 4d postWPP
 
 3289
adult male 01day
 
 1822
adult male 05day
 
 1479
adult male 30day
 
 1418
adult female 01day
 
 1912
adult female 05day
 
 1320
adult female 30day
 
 1357
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
Linear, scaled to Very low expression
Developmental Stage   Expression Level
embryo 00-02hr
 (1687)
embryo 02-04hr
 (3145)
embryo 04-06hr
 (3190)
embryo 06-08hr
 (2434)
embryo 08-10hr
 (2296)
embryo 10-12hr
 (1605)
embryo 12-14hr
 (1878)
embryo 14-16hr
 (2105)
embryo 16-18hr
 (2557)
embryo 18-20hr
 (2374)
embryo 20-22hr
 (2405)
embryo 22-24hr
 (2288)
larva L1
 (1630)
larva L2
 (1124)
larva L3 12hr old
 (1145)
larva L3 puffstage 1-2
 (553)
larva L3 puffstage 3-6
 (1005)
larva L3 puffstage 7-9
 (1064)
white prepupae new
 (1074)
white prepupae 12hr
 (957)
white prepupae 24hr
 (1323)
pupae 2d postWPP
 (1627)
pupae 3d postWPP
 (2783)
pupae 4d postWPP
 (3289)
adult male 01day
 (1822)
adult male 05day
 (1479)
adult male 30day
 (1418)
adult female 01day
 (1912)
adult female 05day
 (1320)
adult female 30day
 (1357)
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
Linear, scaled to Moderate expression
Developmental Stage   Expression Level
embryo 00-02hr
 (1687)
embryo 02-04hr
 (3145)
embryo 04-06hr
 (3190)
embryo 06-08hr
 (2434)
embryo 08-10hr
 (2296)
embryo 10-12hr
 (1605)
embryo 12-14hr
 (1878)
embryo 14-16hr
 (2105)
embryo 16-18hr
 (2557)
embryo 18-20hr
 (2374)
embryo 20-22hr
 (2405)
embryo 22-24hr
 (2288)
larva L1
 (1630)
larva L2
 
 1124
larva L3 12hr old
 
 1145
larva L3 puffstage 1-2
 
 553
larva L3 puffstage 3-6
 
 1005
larva L3 puffstage 7-9
 
 1064
white prepupae new
 
 1074
white prepupae 12hr
 
 957
white prepupae 24hr
 
 1323
pupae 2d postWPP
 (1627)
pupae 3d postWPP
 (2783)
pupae 4d postWPP
 (3289)
adult male 01day
 (1822)
adult male 05day
 1479
adult male 30day
 1418
adult female 01day
 (1912)
adult female 05day
 
 1320
adult female 30day
 
 1357
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
Linear, scaled to High expression
Developmental Stage   Expression Level
embryo 00-02hr
 
 1687
embryo 02-04hr
 
 3145
embryo 04-06hr
 
 3190
embryo 06-08hr
 
 2434
embryo 08-10hr
 
 2296
embryo 10-12hr
 
 1605
embryo 12-14hr
 
 1878
embryo 14-16hr
 
 2105
embryo 16-18hr
 
 2557
embryo 18-20hr
 
 2374
embryo 20-22hr
 
 2405
embryo 22-24hr
 
 2288
larva L1
 
 1630
larva L2
 
 1124
larva L3 12hr old
 
 1145
larva L3 puffstage 1-2
 
 553
larva L3 puffstage 3-6
 
 1005
larva L3 puffstage 7-9
 
 1064
white prepupae new
 
 1074
white prepupae 12hr
 
 957
white prepupae 24hr
 
 1323
pupae 2d postWPP
 
 1627
pupae 3d postWPP
 
 2783
pupae 4d postWPP
 
 3289
adult male 01day
 
 1822
adult male 05day
 
 1479
adult male 30day
 
 1418
adult female 01day
 
 1912
adult female 05day
 
 1320
adult female 30day
 
 1357
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
 High 
 Very high 
Linear, scaled to Extremely high expression
Developmental Stage   Expression Level
embryo 00-02hr
 
 1687
embryo 02-04hr
 
 3145
embryo 04-06hr
 
 3190
embryo 06-08hr
 
 2434
embryo 08-10hr
 
 2296
embryo 10-12hr
 
 1605
embryo 12-14hr
 
 1878
embryo 14-16hr
 
 2105
embryo 16-18hr
 
 2557
embryo 18-20hr
 
 2374
embryo 20-22hr
 
 2405
embryo 22-24hr
 
 2288
larva L1
 
 1630
larva L2
 
 1124
larva L3 12hr old
 
 1145
larva L3 puffstage 1-2
 
 553
larva L3 puffstage 3-6
 
 1005
larva L3 puffstage 7-9
 
 1064
white prepupae new
 
 1074
white prepupae 12hr
 
 957
white prepupae 24hr
 
 1323
pupae 2d postWPP
 
 1627
pupae 3d postWPP
 
 2783
pupae 4d postWPP
 
 3289
adult male 01day
 
 1822
adult male 05day
 
 1479
adult male 30day
 
 1418
adult female 01day
 
 1912
adult female 05day
 
 1320
adult female 30day
 
 1357
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
 High 
 Very high 
 Extremely high 
log, scaled to maximum FBgn0001624 expression level
Developmental Stage   Expression Level
embryo 00-02hr
 
 1687
embryo 02-04hr
 
 3145
embryo 04-06hr
 
 3190
embryo 06-08hr
 
 2434
embryo 08-10hr
 
 2296
embryo 10-12hr
 
 1605
embryo 12-14hr
 
 1878
embryo 14-16hr
 
 2105
embryo 16-18hr
 
 2557
embryo 18-20hr
 
 2374
embryo 20-22hr
 
 2405
embryo 22-24hr
 
 2288
larva L1
 
 1630
larva L2
 
 1124
larva L3 12hr old
 
 1145
larva L3 puffstage 1-2
 
 553
larva L3 puffstage 3-6
 
 1005
larva L3 puffstage 7-9
 
 1064
white prepupae new
 
 1074
white prepupae 12hr
 
 957
white prepupae 24hr
 
 1323
pupae 2d postWPP
 
 1627
pupae 3d postWPP
 
 2783
pupae 4d postWPP
 
 3289
adult male 01day
 
 1822
adult male 05day
 
 1479
adult male 30day
 
 1418
adult female 01day
 
 1912
adult female 05day
 
 1320
adult female 30day
 
 1357
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
 High 
log, scaled to Very low expression
Developmental Stage   Expression Level
embryo 00-02hr
 (1687)
embryo 02-04hr
 (3145)
embryo 04-06hr
 (3190)
embryo 06-08hr
 (2434)
embryo 08-10hr
 (2296)
embryo 10-12hr
 (1605)
embryo 12-14hr
 (1878)
embryo 14-16hr
 (2105)
embryo 16-18hr
 (2557)
embryo 18-20hr
 (2374)
embryo 20-22hr
 (2405)
embryo 22-24hr
 (2288)
larva L1
 (1630)
larva L2
 (1124)
larva L3 12hr old
 (1145)
larva L3 puffstage 1-2
 (553)
larva L3 puffstage 3-6
 (1005)
larva L3 puffstage 7-9
 (1064)
white prepupae new
 (1074)
white prepupae 12hr
 (957)
white prepupae 24hr
 (1323)
pupae 2d postWPP
 (1627)
pupae 3d postWPP
 (2783)
pupae 4d postWPP
 (3289)
adult male 01day
 (1822)
adult male 05day
 (1479)
adult male 30day
 (1418)
adult female 01day
 (1912)
adult female 05day
 (1320)
adult female 30day
 (1357)
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
log, scaled to Moderate expression
Developmental Stage   Expression Level
embryo 00-02hr
 1687
embryo 02-04hr
 (3145)
embryo 04-06hr
 (3190)
embryo 06-08hr
 2434
embryo 08-10hr
 2296
embryo 10-12hr
 1605
embryo 12-14hr
 1878
embryo 14-16hr
 2105
embryo 16-18hr
 (2557)
embryo 18-20hr
 2374
embryo 20-22hr
 2405
embryo 22-24hr
 2288
larva L1
 1630
larva L2
 
 1124
larva L3 12hr old
 
 1145
larva L3 puffstage 1-2
 
 553
larva L3 puffstage 3-6
 
 1005
larva L3 puffstage 7-9
 
 1064
white prepupae new
 
 1074
white prepupae 12hr
 
 957
white prepupae 24hr
 
 1323
pupae 2d postWPP
 1627
pupae 3d postWPP
 (2783)
pupae 4d postWPP
 (3289)
adult male 01day
 1822
adult male 05day
 1479
adult male 30day
 1418
adult female 01day
 1912
adult female 05day
 
 1320
adult female 30day
 
 1357
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
log, scaled to High expression
Developmental Stage   Expression Level
embryo 00-02hr
 
 1687
embryo 02-04hr
 
 3145
embryo 04-06hr
 
 3190
embryo 06-08hr
 
 2434
embryo 08-10hr
 
 2296
embryo 10-12hr
 
 1605
embryo 12-14hr
 
 1878
embryo 14-16hr
 
 2105
embryo 16-18hr
 
 2557
embryo 18-20hr
 
 2374
embryo 20-22hr
 
 2405
embryo 22-24hr
 
 2288
larva L1
 
 1630
larva L2
 
 1124
larva L3 12hr old
 
 1145
larva L3 puffstage 1-2
 
 553
larva L3 puffstage 3-6
 
 1005
larva L3 puffstage 7-9
 
 1064
white prepupae new
 
 1074
white prepupae 12hr
 
 957
white prepupae 24hr
 
 1323
pupae 2d postWPP
 
 1627
pupae 3d postWPP
 
 2783
pupae 4d postWPP
 
 3289
adult male 01day
 
 1822
adult male 05day
 
 1479
adult male 30day
 
 1418
adult female 01day
 
 1912
adult female 05day
 
 1320
adult female 30day
 
 1357
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
 High 
 Very high 
log, scaled to Extremely high expression
Developmental Stage   Expression Level
embryo 00-02hr
 
 1687
embryo 02-04hr
 
 3145
embryo 04-06hr
 
 3190
embryo 06-08hr
 
 2434
embryo 08-10hr
 
 2296
embryo 10-12hr
 
 1605
embryo 12-14hr
 
 1878
embryo 14-16hr
 
 2105
embryo 16-18hr
 
 2557
embryo 18-20hr
 
 2374
embryo 20-22hr
 
 2405
embryo 22-24hr
 
 2288
larva L1
 
 1630
larva L2
 
 1124
larva L3 12hr old
 
 1145
larva L3 puffstage 1-2
 
 553
larva L3 puffstage 3-6
 
 1005
larva L3 puffstage 7-9
 
 1064
white prepupae new
 
 1074
white prepupae 12hr
 
 957
white prepupae 24hr
 
 1323
pupae 2d postWPP
 
 1627
pupae 3d postWPP
 
 2783
pupae 4d postWPP
 
 3289
adult male 01day
 
 1822
adult male 05day
 
 1479
adult male 30day
 
 1418
adult female 01day
 
 1912
adult female 05day
 
 1320
adult female 30day
 
 1357
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
 High 
 Very high 
 Extremely high 
Heatmap
Developmental Stage   Expression Level
embryo 00-02hr
 
 
embryo 02-04hr
 
 
embryo 04-06hr
 
 
embryo 06-08hr
 
 
embryo 08-10hr
 
 
embryo 10-12hr
 
 
embryo 12-14hr
 
 
embryo 14-16hr
 
 
embryo 16-18hr
 
 
embryo 18-20hr
 
 
embryo 20-22hr
 
 
embryo 22-24hr
 
 
larva L1
 
 
larva L2
 
 
larva L3 12hr old
 
 
larva L3 puffstage 1-2
 
 
larva L3 puffstage 3-6
 
 
larva L3 puffstage 7-9
 
 
white prepupae new
 
 
white prepupae 12hr
 
 
white prepupae 24hr
 
 
pupae 2d postWPP
 
 
pupae 3d postWPP
 
 
pupae 4d postWPP
 
 
adult male 01day
 
 
adult male 05day
 
 
adult male 30day
 
 
adult female 01day
 
 
adult female 05day
 
 
adult female 30day
 
 

FlyAtlas Anatomical Expression Data for FBgn0001624


   Styles
Linear
Logarithmic
Heatmap
Back-to-back
   Scales
max expr for FBgn0001624
Moderate expression bin max
High level expression bin max
Very high expression bin max

Summary of FlyAtlas Anatomical Expression Data: Two or more Affy2 ProbeSets identify exons of this gene. This is a summary of the tissue expression peaks exhibited in at least one of these ProbeSets. Expression in all larval and adult organs/tissues ranges from low to undetected. Expression at high levels in the following post-embryonic organs or tissues: adult eye. Expression at moderate levels in the following post-embryonic organs or tissues: adult head, larval/adult central nervous system, adult crop, larval/adult hindgut, adult heart, adult fat body, larval/adult salivary gland, larval trachea, adult ovary, adult male accessory gland, larval/adult carcass.
[download data (TSV)]

Guide to FlyAtlas expression level colors
 
No expression (0 - 9.999)
 
Low expression (10 - 99.999)
 
Moderate expression (100 - 499.999)
 
High level expression (500 - 999.999)
 
Very high expression (1000 - 25000)

Heatmap
Tissue   Expression Level
Larval Central Nervous System no informative data
Larval Midgut no informative data
Larval Hindgut no informative data
Larval Malpighian Tubules no informative data
Larval Fat Body no informative data
Larval Salivary Gland no informative data
Larval Trachea no informative data
Larval Carcass no informative data
Adult Head no informative data
Adult Eye no informative data
Adult Brain no informative data
Adult Thoracic-Abdominal Ganglion no informative data
Adult Crop no informative data
Adult Midgut no informative data
Adult Hindgut no informative data
Adult Malpighian Tubules no informative data
Adult Fat Body no informative data
Adult Salivary Gland no informative data
Adult Heart no informative data
Adult VirginFemale Spermatheca no informative data
Adult InseminatedFemale Spermatheca no informative data
Adult Ovary no informative data
Adult Testis no informative data
Adult Male Accessory Gland no informative data
Adult Carcass no informative data

modENCODE Temporal Expression Data (Graveley et al., 2011)
FlyAtlas Anatomical Expression Data (Chintapalli et al., 2007)
hide Expression Clusters
A cluster of genes with similar mRNA expression dynamics across development.
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Linkouts
FLIGHT - Cell culture data for RNAi and other high-throughput technologies
FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
hide Alleles & Phenotypes
hide Summary of Allele Phenotypes
Lethality
Allele
Other Phenotypes
Allele
Phenotype manifest in
Allele
imaginal disc & epithelial cell & plasma membrane | somatic clone
imaginal disc & epithelial cell & septate junction | somatic clone
imaginal disc & septate junction
neuromuscular junction & bouton
neuromuscular junction & postsynaptic membrane
postsynaptic membrane & neuromuscular junction | larval stage
presynaptic membrane & neuromuscular junction | larval stage
type I bouton & synaptic vesicle & third instar larva (with Df(1)N71)
hide Classical Alleles ( 57 )
For All Classical Alleles Show

Allele of dlg1ClassMutagenStocksKnown lesion
dlg1G02762 --
dlg1G03422 --
dlg114amorphic allele - genetic evidence, loss of function allele1 Yes
dlg118hypomorphic allele - genetic evidence1 Yes
dlg12hypomorphic allele - genetic evidence1 Yes
dlg15-HA-1959
1 --
dlg15hypomorphic allele - genetic evidence1 --
dlg161 Yes
dlg1CB-5424-3
1 --
dlg1d087531 --
dlg1d107471 --
dlg1e036221 --
dlg1EY05003
1 --
dlg1f03974
1 --
dlg1f079371 --
dlg1G04561 --
dlg1NP1102
1 --
dlg1NP4134
1 --
dlg1NP7225
1 --
dlg1100 --
dlg1110 --
dlg1120 Yes
dlg1130 --
dlg115loss of function allele0 --
dlg116
0 --
dlg117
0 --
dlg1190 --
dlg110 --
dlg130 --
dlg140 --
dlg17loss of function allele, hypomorphic allele - genetic evidence0 Yes
dlg180 --
dlg190 --
dlg1A-51.10 Yes
dlg1A40.20 Yes
dlg1b88
0 Yes
dlg1CC019360 Yes
dlg1CPTI0002070 Yes
dlg1CPTI0025690 Yes
dlg1CPTI0028600 Yes
dlg1G40 --
dlg1G50 --
dlg1G60 --
dlg1G70 --
dlg1G80 --
dlg1G90 --
dlg1GG01705
0 --
dlg1misb
0 --
dlg1PG1000 --
dlg1PL320 --
dlg1S97-1380 Yes
dlg1S97-50 Yes
dlg1S97-flpV0 Yes
dlg1S97-rev1500 Yes
dlg1sw
0 Yes
dlg1unspecified
0 --
dlg1w55
0 --
hide Alleles Carried on Transgenic Constructs ( 42 )
For All Alleles Carried on Transgenic Constructs Show

Allele of dlg1ClassMutagenStocksKnown lesion
dlg1GD46892 Yes
dlg1GL001881 Yes
dlg1HMS000141 Yes
dlg1HMS000241 Yes
dlg1HMS001721 Yes
dlg1HMS015211 Yes
dlg1JF010761 Yes
dlg1JF010771 Yes
dlg1JF013651 Yes
dlg1JF016941 Yes
dlg1a.S97N0 Yes
dlg1cQa0 Yes
dlg1dsRNA.cBa0 Yes
dlg1HOOK.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1KK1162850 Yes
dlg1PDZ2+HOOK.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1S48A.Scer\UAS.T:Avic\GFP0 Yes
dlg1S48D.Scer\UAS.T:Avic\GFP0 Yes
dlg1S97N.Scer\UAS.T:Avic\GFP-EGFP0 Yes
dlg1S97N0 Yes
dlg1SA.Scer\UAS.T:Avic\GFP0 Yes
dlg1Scer\UAS.cBa0 Yes
dlg1Scer\UAS.T:Avic\GFP-YFP0 Yes
dlg1Scer\UAS.T:Avic\GFP0 Yes
dlg1SD.Scer\UAS.T:Avic\GFP0 Yes
dlg1WT.Scer\UAS.T:Avic\GFP-EGFP0 Yes
dlg1WT.Scer\UAS.T:Avic\GFP0 Yes
dlg1ΔC1:2.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔE-F.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔGUK.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔHOOK.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔI3.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔN.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔN2:3.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔPDZ1.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔPDZ1:2.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔPDZ1:3.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔPDZ2.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔPDZ2:3.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔPDZ3.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1ΔSH3.Scer\UAS.T:Zzzz\FLAG0 Yes
dlg1Δt40.Scer\UAS.T:Zzzz\FLAG0 Yes
hide Aneuploid Aberrations
Duplicated in
Not disrupted in
Not duplicated in
Disrupted in
hide Transgenic Constructs & Insertions
Transgenic Constructs
Type of construct
Name
Expression data
Insertions
Type of insertions
Name
Expression data
insertion of enhancer trap binary system
hide Gene Ontology: Function, Process & Cellular Component ( 51 unique terms )
hide Terms Based on Experimental Evidence ( 28 terms )
Molecular Function
CV term
References
inferred from physical interaction with gukh
Biological Process
CV term
References
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
Cellular Component
CV term
References
inferred from direct assay
inferred from direct assay
inferred from direct assay
inferred from mutant phenotype
inferred from direct assay
colocalizes_with
postsynaptic membrane
inferred from direct assay
colocalizes_with
presynaptic membrane
inferred from direct assay
inferred from direct assay
inferred from direct assay
hide Terms Based on Predictions or Assertions ( 28 terms )
Molecular Function
CV term
References
Biological Process
CV term
References
traceable author statement
non-traceable author statement
non-traceable author statement
traceable author statement
non-traceable author statement
Cellular Component
CV term
References
non-traceable author statement
traceable author statement
non-traceable author statement
traceable author statement
hide Sequence Ontology: Class of Gene
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hide Summary of Physical Interactions
Protein-protein
Interacting group
Assay
References
hide Summary of Genetic Interactions
Interacts with
Please look at the allele data for full details of the genetic interactions
dlg1 allele
Gene
References
hide External Data
Linkouts
BioGRID - A database of protein and genetic interactions
DPiM - DPiM, Drosophila Protein interaction Map
DroID - A comprehensive database of gene and protein interactions.
InterologFinder Protein-protein interactions (PPI) from both known and predicted PPI data sets.
hide Orthologs
Genome-wide drosophilid orthologs
Curated drosophilid orthologs
Linkouts
InParanoid A subset of ortholog calls from InParanoid.
OrthoDB (Arthropod subset) The hierarchical catalog of eukaryotic orthologs.
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hide Stocks Listed in FlyBase ( 32 )
Bloomington
Harvard
Kyoto
VDRC
hide Genomic Clones ( 2 )
Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete
hide cDNA Clones ( 199 )
Please Note
This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see GBrowse for alignment of the cDNAs and ESTs to the gene model.
cDNA Clones, Fully Sequenced
BDGP DGC clones
Other clones
cDNA Clones, End Sequenced (ESTs)
BDGP DGC clones
Other clones
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Linkouts
DRSC - Results from RNAi screens.
GenomeRNAi - GenomeRNAi – A database for cell-based and in vivo RNAi phenotypes and reagents
hide Antibody Information
polyclonal antibody
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hide Relationship to Other Genes
Source for database identity of
Source for identity of: dlg1 CG1725
Source for database merge of
Source for merge of: dlg1 anon-EST:Posey93
Source for merge of: dlg1 anon-WO03040301.258 anon-WO03040301.260 anon-WO03040301.268
Source for merge of: dlg1 CG1730
Source for merge of: dlg1 l(1)G0276 l(1)G0456 l(1)G0342
Additional comments
Annotations CG1725 and CG1730 merged as CG1725 in release 3 of the genome annotation.
Source for merge of dlg1 anon-WO03040301.258 anon-WO03040301.260 anon-WO03040301.268 was sequence comparison (date:051113).
hide Other Comments
dlg1 protein is required for the microtubule-induced cortical polarity of the raps and G-iα65A proteins in neuroblasts.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
Vap-33-1 and dlg1 localize asymmetrically at the synapse during bouton budding.
baz, raps and dlg1 establish and maintain planar polarity in pI cells.
The l(2)gl and dlg1 products act in a common process that differentially mediates cortical protein targeting in mitotic neuroblasts, creating intrinsic differences between daughter cells.
The dlg1 product regulates the localization of l(2)gl.
The l(2)gl and dlg1 gene products regulate basal protein targeting, but not apical complex formation or spindle orientation, in both embryonic and larval neuroblasts. The l(2)gl and dlg1 proteins promote, and that of zip inhibits, actomyosin dependent basal protein targeting in neuroblasts.
dlg1 and CaMKII protein colocalise at synapses and exist in the same protein complex.
Functional analysis of the MAGUK domains of dlg1 in vivo.
The dlg1 gene product is not required for the localization of glutamate receptors at synapses.
The dlg1 product colocalises with Sh K+ channels, which are clustered at glutamatergic synapses at the larval neuromuscular junction. Results demonstrate dlg1 plays an important role in synaptic organisation in vivo that correlates with its ability to bind directly to specific membrane proteins of the synapse.
Some of the proteins of apico-lateral junctions are required both for apico-basal cell polarity and for the signalling mechanisms controlling cell proliferation, whereas others are required more specifically in cell-cell signalling.
The C-terminal sequences of Fas2 and Sh are both necessary and sufficient for targeting to the subsynaptic muscle membrane at the larval neuromuscular junction, and this localization depends on the product of dlg1.
Mutations in dlg1 can result in postsynaptic structural defects and large synaptic currents at neuromuscular junctions. Targetted expression of dlg1 using Scer\GAL4 can substantially rescue the reduced postsynaptic structure and presynaptic expression can rescue the physiological defect. Levels of postsynaptic dlg1 regulate or determine subsynaptic reticulum (SSR) size. Results suggest that dlg1 functions in the regulation of neurotransmitter release and postsynaptic structure.
The expression of dlg1 during synaptogenesis and synapse maturation has been studied.
dlg1 protein is localised on the cytoplasmic face of the septate junction and is required for the maintenance of this structure. dlg1 is also required for proper organisation of the cytoskeleton, for the differential location of membrane proteins and for apicobasal polarity of epithelial cells. These functions can be uncoupled from dlg1s role as a tumour suppressor since mutations in two domains of the protein (SH3 and GUK) cause loss of normal cell proliferation control without affecting the other functions of the protein.
Drosophila homolog of rat PSD-95.
In addition to its function as a tumor suppressor, the dlg1 gene is required for proper formation of neuromuscular synapses.
dlg1 immunoreactivity is expressed at one type of glutamatergic synapse and is associated with both presynaptic and postsynaptic membranes. Mutations in dlg1 alter the expression and cause striking changes in the structure of the subsynaptic reticulum, a postsynaptic specialisation at these synapses. Results indicate that dlg1 is required for normal synaptic structure.
Mutants display an imaginal disc neoplastic phenotype.
Endocrine mechanisms responsible for the prolongation of larval life in dlg1 mutants have been investigated: results suggest that delayed pupariation is caused by the overgrown imaginal discs inhibiting the production or release of ecdysteroids from the endocrine system.
Reduced ecdysteroid titer and delayed or blocked metamorphosis in mutants may be a result of altered neuropeptide production, which is probably secondary to the imaginal disc overgrowth.
Mutant analysis of dlg1 suggests that cell-cell interaction and communication is required for the termination of disc cell proliferation. This must occur prior to cellular response to ecdysone.
Mutations cause neoplastic imaginal overgrowth.
A protein, PSD-95, similar to the dlg1 tumour suppressor protein has been found in the rat brain. dlg1 protein is associated with septate junctions in developing flies and contains a guanylate kinase domain that is required for normal control of cell division.
Mutant analysis demonstrates that the dlg1 gene product is a guanylate kinase homolog located in a small apical belt of the lateral cell membrane coinciding in position with the septate junction.
The developmental profile of dlg1 transcription has been investigated.
dlg1 has been isolated and characterized.
Late larval lethal; prolonged larval stages with bloated larvae attempting pupariation around day 15; some cuticular tanning, but no adult cuticular structures formed. During early larval development, the imaginal discs are smaller than those of normal larvae of the same age and are misshapen, but as the larvae continue to survive after the normal pupariation time, the discs continue to grow. They become large, amorphous and solid, containing three times the normal numbers of cells at ten days of age; they also experience substantial cell death. By eleven days, wing and haltere discs may fuse; also first and second leg discs fuse with ventral ganglion of the CNS; great enlargement of optic lobes of brain also takes place. Discs, but not brains, transplanted into adults grow rapidly displaying invasive growth; they do not differentiate when transplanted into larvae for metamorphosis. Homozygous tissues do not survive, nor do gynandromorphs (one with male abdominal tissue vs. 66 expected). It is possible to produce homozygous germ-line clones (Perrimon, 1988). dlg1 embryos generated from such clones display defects in morphogenesis and neurogenesis; most tissues are defective; partial rescue achieved by a paternal dlg1+ contribution, in the form of either a normal X or a v+Y.
 
hide External Crossreferences & Linkouts
Sequence Crossreferences
RefSeq (Transcripts)
RefSeq (Proteins)
Entrez Gene - A searchable database of RefSeq genes.
Other Crossreferences
InterPro domains - A database of protein families, domains, and functional sites
PDZ/DHR/GLGF (IPR001478)
L27 (IPR004172)
Guanylate kinase (IPR008144)
L27-1 (IPR015143)
Variant SH3 (IPR011511)
Linkouts
BioGRID - A database of protein and genetic interactions
DPiM - DPiM, Drosophila Protein interaction Map
DroID - A comprehensive database of gene and protein interactions.
DRSC - Results from RNAi screens.
FLIGHT - Cell culture data for RNAi and other high-throughput technologies
FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
FlyMine - Integrated genomics database for Drosophila, Anopheles, and C.elegans
GenomeRNAi - GenomeRNAi – A database for cell-based and in vivo RNAi phenotypes and reagents
InParanoid A subset of ortholog calls from InParanoid.
Interactive Fly - A cyberspace guide to Drosophila development and metazoan evolution
InterologFinder Protein-protein interactions (PPI) from both known and predicted PPI data sets.
modMine - Data generated by the modENCODE project.
OrthoDB (Arthropod subset) The hierarchical catalog of eukaryotic orthologs.
hide Synonyms & Secondary IDs ( 60 )
Reported As
Symbol Synonym
anon-EST:Posey93
anon-WO03040301.258
 
anon-WO03040301.260
 
anon-WO03040301.268
 
dlg
(Zhao et al., 2008, Werz et al., 2005, Dunlop et al., 2004, Bachmann et al., 2004, Le Borgne and Schweisguth, 2003, Mendoza et al., 2003, Karunanithi et al., 2002, Brumby et al., 2004, Roegiers and Jan, 2004, Dudu et al., 2004, Zhao et al., 2005, Goode et al., 2005, Cho, 2005, Bilder, 2004, Szafranski and Goode, 2004, Kuppers-Munther et al., 2004, Pagliarini and Xu, 2003, Gibson and Perrimon, 2003, Wodarz and Huttner, 2003, Radovic and Bryant, 2003, Doe and Bowerman, 2001, Johnson and Wodarz, 2003, Lecuit and Pilot, 2003, Bilder et al., 2003, Tanentzapf and Tepass, 2003, Albertson and Doe, 2003, Kaltschmidt et al., 2002, Medina et al., 2002, Humbert et al., 2003, Drapeau et al., 2003, Abdelilah-Seyfried et al., 2003, Chia and Yang, 2002, Adler, 2002, Greaves, 2001, Doe, 2001, Goode, 2000, Caruana, 2002, Schaefer and Knoblich, 2001, Muller, 2003, Wedlich, 2002, Cross et al., 2003, Papagiannouli et al., 2003, Marhold et al., 2003, Pennetta et al., 2002, Kaufmann et al., 2002, Cross et al., 2002, Marhold et al., 2002, Leeds and Coyle-Thompson, 2002, Mathew et al., 2001, Kuchinke et al., 2001, Karunanithi et al., 2001, Wodarz, 2001, Johnston and Gallant, 2002, Tepass et al., 2001, Hardie and Raghu, 2001, Wu et al., 2001, Luxenberg et al., 2001, Bellaiche et al., 2001, Bilder, 2001, Radovic et al., 2001, Ramon and Coyle-Thompson, 2001, Tanentzapf and Tepass, 2001, Ohshiro et al., 2001, Peng et al., 2000, Ohshiro et al., 2000, Greaves, 2000, Wodarz, 2000, Thomas et al., 2000, Sone et al., 2000, Peifer, 2000, Muller, 2000, Dobens and Raftery, 2000, Bilder et al., 2000, Littleton and Ganetzky, 2000, Andrew et al., 2000, Ramon et al., 2000, Radovic et al., 2000, Atwood et al., 1999, Turenchalk et al., 1999, Greaves et al., 1999, Bilder et al., 1999, Koh et al., 1999, Torroja et al., 1999, Prokop, 1999, Rohrbough et al., 1999, McGee and Bredt, 1999, Kim and Huganir, 1999, Jesu et al., 1999, Bilder and Perrimon, 1999, Agnes and Noselli, 1999, Kondo, 1998, Gundelfinger et al., 1998, Woods et al., 1998, Craven and Bredt, 1998, Woodhouse et al., 1998, Ward et al., 1998, Jesu et al., 1998, Jesu et al., 1998, Biessmann and Walter, 1998, Petersen et al., 1997, Noselli, 1998, Hough et al., 1997, Bryant, 1993, Zito et al., 1997, Thomas et al., 1997, Ruiz-Cathada et al., 1997, Kim, 1997, Izaddoost et al., 1997, Thomas et al., 1997, Sheng and Wyszynski, 1997, Goode and Perrimon, 1997, Makino et al., 1997, Littlejohn et al., 1997, Ponting et al., 1997, Woods et al., 1997, Trimmer and Rhodes, 1997, Dimitratos et al., 1997, Bryant, 1997, Budnik, 1996, Brunner and O'Kane, 1997, Goode and Perrimon, 1997, Fagotto and Gumbiner, 1996, Fanning and Anderson, 1996, Woods et al., 1996, Budnik et al., 1996, Guan et al., 1996, Kim, 1995, Peifer, 1996, Hough et al., 1996, Budnik et al., 1995, Kirkpatrick and Peifer, 1995, Watson et al., 1994, Shieh and Niemeyer, 1995, Mechler, 1994, Gateff, 1994, Goode and Perrimon, 1995, Woods and Bryant, 1993, Peifer et al., 1993, Bryant et al., 1993, Woods and Bryant, 1993, Boedigheimer et al., 1993, Binari and Perrimon, 1994, Sehnal and Bryant, 1993, Garner et al., 1993, Skaer, 1993, Zitnan et al., 1993, Koonin et al., 1992, Woods and Bryant, 1992, Woods and Bryant, 1991, Bryant and Schmidt, 1990, Richardson et al., 2005, Zhao et al., 2006, Szafranski and Goode, 2006, Hall et al., 2006, Denef et al., 2006, Wirtz-Peitz and Knoblich, 2006, Humbert et al., 2006, Wodarz and Gonzalez, 2006, Djiane et al., 2005, Janody and Treisman, 2006, Emery et al., 2005, Mathew et al., 2002, Wiggin et al., 2005, Mendoza-Topaz et al., 2008, Guthridge et al., 2007, Tountas and Fortini, 2007, D'Costa et al., 2006, Goode et al., 2005, Bao et al., 2007, Yang et al., 2005, Lecuit, 2004, Chia et al., 2008, Wei et al., 2004, Hackney et al., 2007, Gorczyca et al., 2007, Laprise et al., 2006, Jankovics and Brunner, 2006, Denef et al., 2008, Zhang et al., 2007, Heckscher et al., 2007, Pielage et al., 2008, Rodal et al., 2008, Blankenship et al., 2007, Moyer and Jacobs, 2008, Donlea et al., 2009, Ohsawa et al., 2011, Courbard et al., 2009, Igaki et al., 2006, Igaki et al., 2006, Grosskortenhaus et al., 2005, Viquez et al., 2006, Katsuki et al., 2009, Ni et al., 2009, Kohsaka et al., 2007, Li et al., 2009, Laprise et al., 2010, Grzeschik et al., 2010, Franz and Riechmann, 2010, Walther and Pichaud, 2010, Cordero et al., 2010, Mao and Freeman, 2009, Fichelson et al., 2010, Simone and DiNardo, 2010, Bahri et al., 2010, Bachmann et al., 2010, Bachmann et al., 2010, Garlena et al., 2010, Fernandez-Minan et al., 2008, Grifoni et al., 2004, Dow et al., 2003, Buchon et al., 2010, Kaplan et al., 2009, Kitajima et al., 2010, Thomson and Johnson, 2010, Albornoz et al., 2008, Letizia et al., 2011, Pastor-Pareja et al., 2008, Cabernard et al., 2010)
DLG
(Liebl et al., 2005, Singh et al., 2005, Montana and Littleton, 2004, Genova and Fehon, 2003, Koh et al., 2002, Rosin et al., 2004, Rieckhof et al., 2003, Packard et al., 2003, Benton and St. Johnston, 2003, Schenck et al., 2003, Cereijido et al., 2003, Van Doren et al., 2003, Rushton et al., 2003, Packard et al., 2002, Beumer et al., 2002, Radovic et al., 2002, Kazantsev et al., 2002, Razzaq et al., 2001, Renden et al., 2001, Mathew et al., 2001, Parmentier et al., 2001, Beumer et al., 2001, Kramer, 2000, Bellen, 2000, Seidensticker and Behrens, 2000, Murthy, 1999, Beumer et al., 1999, O'Brien et al., 1998, Parmentier et al., 1999, Gorczyca et al., 1999, Bhat et al., 1999, Koh et al., 1999, Montell, 1998, Baumgartner et al., 1996, Roush, 1996, Thompson and Cohen, 2006, Hiesinger et al., 2005, Dickman et al., 2006, Dickman, 2006, Ataman, 2006, Ashraf et al., 2006, Wang et al., 2006, Rivlin et al., 2004, Ohyama et al., 2007, Haas et al., 2007, Liebl et al., 2008, Ash et al., 2007, Pan et al., 2008, Acharya et al., 2006, Margolis and Borg, 2005, Aravamudan and Broadie, 2003, Pallavi and Shashidhara, 2005, Hebbar et al., 2006, Chen and Featherstone, 2005, Kapelnikov et al., 2008, Cauchi et al., 2008, Kumar et al., 2009, Gilestro et al., 2009, Ramachandran et al., 2009, Beramendi et al., 2007, Rushton et al., 2009, Korkut et al., 2009, Chang et al., 2008, Dickman and Davis, 2009, Fuentes-Medel et al., 2009, Gibson et al., 2011, Ratnaparkhi et al., 2008, Kolodziejczyk et al., 2008, Milton et al., 2010, Mosca and Schwarz, 2010, Kim et al., 2010, Choi et al., 2010, Hamanaka and Meinertzhagen, 2010, Chiang et al., 2011, Morimoto et al., 2010, Varija Raghu et al., 2011, Uytterhoeven et al., 2011, Beerman and Jongens, 2011, Wu et al., 2011, Shih and Chiang, 2011, Lanson et al., 2011)
Dlg
(Araujo et al., 2005, Munoz-Descalzo et al., 2005, Masuda-Nakagawa et al., 2005, Ferres-Marco et al., 2006, Xu et al., 2005, Pielage et al., 2005, Albin and Davis, 2004, Cho, 2004, Lee et al., 2003, Udan et al., 2003, Rolls et al., 2003, Vaccari et al., 2005, Grosshans et al., 2005, Lim and Choi, 2004, Kato et al., 2004, van Roessel et al., 2004, Wu et al., 2004, Schulte et al., 2003, Roche et al., 2002, Wu and Beitel, 2004, Betschinger and Knoblich, 2004, Strickland and Burgess, 2004, Wu et al., 2005, Hall et al., 2005, Torban et al., 2004, Koh et al., 2004, Bachmann et al., 2003, Horton and Ehlers, 2003, Coyle et al., 2004, Bardin et al., 2004, Wu et al., 2004, Bellaiche et al., 2004, Llimargas et al., 2004, Lim and Choi, 2003, Siegrist and Doe, 2004, Mueller and Bossinger, 2003, Anonymous, 2003, Bilder, 2003, Hoover and Bryant, 2000, Lecuit, 2003, Henrique and Schweisguth, 2003, Bastock et al., 2003, Braga and Harwood, 2001, Bryant and Huwe, 2000, Nelson, 2003, Hemphala et al., 2003, Knust and Bossinger, 2002, Goode and Szafranski, 2003, Zhao et al., 2003, Deng et al., 2003, Kango-Singh et al., 2002, Knox and Brown, 2002, Chern and Choi, 2002, Hebbar and Fernandes, 2002, Hering and Sheng, 2002, Hoover and Bryant, 2002, Verstreken et al., 2002, Aberle et al., 2002, Leventis et al., 2001, Hong et al., 2001, Zelhof et al., 2001, Chase, 2001, Knust, 2001, Bilder, 2001, Bellaiche et al., 2001, Mayer, 2001, Zahraoui et al., 2001, Bienz and Clevers, 2000, Zahraoui et al., 2000, Cho, 2000, Huwe et al., 2000, Dimitratos et al., 1999, Martinez Arias et al., 1999, Yeaman et al., 1999, Noselli and Agnes, 1999, Radovic' et al., 1999, Tsunoda et al., 1998, Craven and Bredt, 1998, Broadie, 1998, Anonymous, 1998, Anonymous, 1998, Brosamle, 1998, Woods et al., 1997, Tepass, 1997, Woods et al., 1997, Woods et al., 1996, Anderson, 1996, Fanning et al., 1993, Wang et al., 2006, Auld et al., 2006, Bogdanik et al., 2008, Le Bivic, 2005, Singh et al., 2006, Dudu, 2006, Siddall et al., 2006, Thompson and Cohen, 2006, McCartney et al., 2006, Muro et al., 2006, Ahringer, 2005, Siegrist and Doe, 2005, Kim et al., 2006, Nolo et al., 2006, Poulton and Deng, 2006, Wei et al., 2005, Harris and Peifer, 2004, Mahr and Aberle, 2006, Dudu et al., 2006, Mirkovic and Mlodzik, 2006, Sommer et al., 2005, Wang et al., 2006, Koh et al., 2007, Schneider et al., 2006, Simoes et al., 2006, Qian and Prehoda, 2006, Pfleger et al., 2007, Bennett and Harvey, 2006, Kolsch et al., 2007, Tian and Ten Hagen, 2007, Tiwari and Roy, 2009, Yu et al., 2008, Merino et al., 2009, Banovic et al., 2010, Stowers and Isacoff, 2007, Langevin et al., 2005, Harris and Peifer, 2005, Sasaki et al., 2007, Nagaraj and Banerjee, 2007, Lovegrove et al., 2006, Bach et al., 2007, Sanchez-Soriano and Prokop, 2005, Lee et al., 2007, Moberg et al., 2005, Meyer and Aberle, 2006, Wu et al., 2007, Pielage et al., 2006, Lee et al., 2002, Jafar-Nejad et al., 2005, Wang et al., 2007, Marques, 2005, Beuchle et al., 2007, Suzuki and Ohno, 2006, Zhao et al., 2007, Murthy et al., 2010, Rohrbough et al., 2007, Szafranski and Goode, 2007, Horne-Badovinac and Bilder, 2008, Menut et al., 2007, Siegrist and Doe, 2006, Harris and Peifer, 2007, Corrigall et al., 2007, Link et al., 2007, Mirouse et al., 2007, Kohsaka et al., 2007, Besse et al., 2007, Albertson et al., 2008, Cao et al., 2008, Grzeschik et al., 2007, Song et al., 2007, Nishimura et al., 2007, Homem and Peifer, 2008, Yasugi et al., 2008, Pope and Harris, 2008, O'Keefe et al., 2007, Conder et al., 2007, Ou et al., 2007, Polesello and Tapon, 2007, O'Connor-Giles et al., 2008, Egger et al., 2007, Banerjee et al., 2008, Vogler and Urban, 2008, Albertson et al., 2004, Bayraktar et al., 2006, Speicher et al., 2008, Walthall et al., 2007, Miech et al., 2008, Chandraratna et al., 2007, Sokac and Wieschaus, 2008, Narasimha et al., 2008, Romani et al., 2009, Schulte et al., 2006, Wairkar et al., 2009, Mirouse et al., 2009, Gorfinkiel and Arias, 2007, Nagaraj and Banerjee, 2009, Campbell et al., 2010, Hamaratoglu et al., 2006, Morrison et al., 2008, Alves-Silva et al., 2008, Korolchuk et al., 2007, Grusche et al., 2009, Rodahl et al., 2009, Widmann and Dahmann, 2009, Giagtzoglou et al., 2009, Ninov et al., 2009, Emes et al., 2008, Peng et al., 2009, Verstreken et al., 2005, Lee et al., 2009, Hamaratoglu et al., 2009, Genevet et al., 2009, Glavic et al., 2009, Laprise et al., 2009, Sekyrova et al., 2010, Peng et al., 2009, Willecke et al., 2008, Baena-Lopez et al., 2008, Sawyer et al., 2009, Woolworth et al., 2009, Lin et al., 2009, Flaherty et al., 2009, Sahota et al., 2009, Massarwa et al., 2009, O'Keefe et al., 2009, Campbell et al., 2009, Yan et al., 2009, Warner and Longmore, 2009, Willecke et al., 2006, Patel et al., 2009, Copeland et al., 2007, Eid et al., 2008, Ly et al., 2008, Kumar et al., 2009, Larson et al., 2008, Guha et al., 2009, Cobreros et al., 2008, Zhang et al., 2009, Warner and Longmore, 2009, Barber et al., 2009, Ogawa et al., 2009, Kim et al., 2009, Langton et al., 2009, Huntwork and Littleton, 2007, Roeth et al., 2009, Pielage et al., 2008, Haines et al., 2007, Martinez et al., 2009, Johnson et al., 2009, Masuda-Nakagawa et al., 2009, Gervais and Casanova, 2010, Krahn et al., 2010, Robinson et al., 2010, Ho et al., 2010, Maynard et al., 2010, Morais-de-Sá et al., 2010, Haglund et al., 2010, Maurel-Zaffran et al., 2010, Lee et al., 2008, Devaud et al., 2008, Fernandes et al., 2010, Yu et al., 2010, Beam and Moberg, 2010, Warner et al., 2010, Chen et al., 2010, Levine et al., 2010, Tamori et al., 2010, Januschke and Gonzalez, 2010, Nelson et al., 2010, Marie et al., 2010, Ekas et al., 2010, Hamel et al., 2010, Graham et al., 2010, Bachmann et al., 2008, Wang and Riechmann, 2007, Zhang et al., 2007, Harumoto et al., 2010, Tikhmyanova et al., 2010, Tsurudome et al., 2010, Daniels et al., 2011, Liu et al., 2010, Padash-Barmchi et al., 2010, Djiane et al., 2011, Kaplan and Tolwinski, 2010, Lee et al., 2010, Roy et al., 2007, Wang et al., 2011, Lee and Thomas, 2011, Müller et al., 2011, Kaplan et al., 2011, Laplante et al., 2010, Hijazi et al., 2011, Nahm et al., 2010, Szul et al., 2011, James and Broihier, 2011, Jiang et al., 2011, Charlton-Perkins et al., 2011, Georgiou and Baum, 2010, Rossetto et al., 2011, Raghu and Borst, 2011, Peng et al., 2009, Khuong et al., 2010, Gilbert et al., 2011, Ball et al., 2010, Ayyub, 2011, Fan et al., 2010, Rohrbough and Broadie, 2010)
l(1)d.lg.-1
l(1)G19
 
l(1)l.pr.-2
 
Name Synonym
Discs large
(Wu et al., 2005, Schneeberger and Raabe, 2003, Gibson and Schubiger, 2001, Chan et al., 2003, Hipfner et al., 2004, Martinez Arias et al., 1999, Muro et al., 2006, Kim et al., 2006, Poulton and Deng, 2006, Harris and Peifer, 2004, Sommer et al., 2005, Bennett and Harvey, 2006, Ash et al., 2007, Stowers and Isacoff, 2007, Sasaki et al., 2007, Sanchez-Soriano and Prokop, 2005, Lecuit, 2004, Suzuki and Ohno, 2006, Hackney et al., 2007, Krieser et al., 2007, Mirouse et al., 2007, Polesello and Tapon, 2007, Chandraratna et al., 2007, Schulte et al., 2006, Blankenship et al., 2007, Hamaratoglu et al., 2009, Laprise et al., 2009, Sahota et al., 2009, Massarwa et al., 2009, O'Keefe et al., 2009, Ribaya et al., 2009, Warner and Longmore, 2009, Patel et al., 2009, Kondo et al., 2007, Guha et al., 2009, Forster et al., 2010, Warner and Longmore, 2009, Kim et al., 2009, Langton et al., 2009, Huntwork and Littleton, 2007, Krahn et al., 2010, Grzeschik et al., 2010, Robinson et al., 2010, Franz and Riechmann, 2010, Maynard et al., 2010, Ratnaparkhi et al., 2008, Kolodziejczyk et al., 2008, Maurel-Zaffran et al., 2010, Warner et al., 2010, Chen et al., 2010, Tamori et al., 2010, Nelson et al., 2010, Hamel et al., 2010, Milton et al., 2010, Simone and DiNardo, 2010, Bahri et al., 2010, Murthy et al., 2010, Kim et al., 2010, Choi et al., 2010, Tsurudome et al., 2010, Padash-Barmchi et al., 2010, Park et al., 2011, Masuda-Nakagawa et al., 2010, Buchon et al., 2010, Lee and Wu, 2010, Kaplan et al., 2009, Syed et al., 2011, Szul et al., 2011, Gilbert et al., 2011, Ayyub, 2011, Rohrbough and Broadie, 2010)
discslarge
lethal(1)benign wing imaginal disc neoplasm
lethal(1)discs large
lethal(2)discs large
Secondary FlyBase IDs
  • FBgn0010108
  • FBgn0027239
  • FBgn0027662
  • FBgn0028321
  • FBgn0029052
  • FBgn0030295
  • FBgn0066811
  • FBgn0066812
  • FBgn0066813
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hide Recent research papers ( 95 )
Ayyub, 2011, J. Genet. 90(2): 239--249
Cullin-5 and cullin-2 play a role in the development of neuromuscular junction and the female germ line of Drosophila. [FBrf0214802]
Beerman and Jongens, 2011, Neuroscience 181: 48--66
A non-canonical start codon in the Drosophila fragile X gene yields two functional isoforms. [FBrf0213401]
Charlton-Perkins et al., 2011, Neural Dev. 6: 20
Prospero and Pax2 combinatorially control neural cell fate decisions by modulating Ras- and Notch-dependent signaling. [FBrf0213993]
Chiang et al., 2011, Curr. Biol. 21(1): 1--11
Three-Dimensional Reconstruction of Brain-wide Wiring Networks in Drosophila at Single-Cell Resolution. [FBrf0212704]
Daniels et al., 2011, Neurobiol. Disease 41(2): 415--420
Increased vesicular glutamate transporter expression causes excitotoxic neurodegeneration. [FBrf0212635]
Djiane et al., 2011, J. Cell Biol. 192(1): 189--200
Su(dx) E3 ubiquitin ligase-dependent and -independent functions of Polychaetoid, the Drosophila ZO-1 homologue. [FBrf0212737]
Gibson et al., 2011, Cell 144(3): 427--438
Control of the mitotic cleavage plane by local epithelial topology. [FBrf0214365]
Gilbert et al., 2011, Dev. Cell 20(5): 700--712
A Screen for Conditional Growth Suppressor Genes Identifies the Drosophila Homolog of HD-PTP as a Regulator of the Oncoprotein Yorkie. [FBrf0213686]
Hijazi et al., 2011, PLoS ONE 6(3): e17763
The ly6 protein coiled is required for septate junction and blood brain barrier organisation in Drosophila. [FBrf0213269]
James and Broihier, 2011, Development 138(15): 3273--3286
Crimpy inhibits the BMP homolog Gbb in motoneurons to enable proper growth control at the Drosophila neuromuscular junction. [FBrf0214390]
Jiang et al., 2011, Oncogene 30(29): 3248--3260
Sds22/PP1 links epithelial integrity and tumor suppression via regulation of myosin II and JNK signaling. [FBrf0214488]
Kaplan et al., 2011, PLoS ONE 6(4): e18616
Complex Interactions between GSK3 and aPKC in Drosophila Embryonic Epithelial Morphogenesis. [FBrf0213424]
Lanson et al., 2011, Hum. Mol. Genet. 20(13): 2510--2523
A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43. [FBrf0213887]
Laplante and Nilson, 2011, J. Cell Biol. 192(2): 335--348
Asymmetric distribution of Echinoid defines the epidermal leading edge during Drosophila dorsal closure. [FBrf0212838]
Lee and Thomas, 2011, Mech. Dev. 128(1-2): 116--128
Rac1 modulation of the apical domain is negatively regulated by β(Heavy)-spectrin. [FBrf0213021]
Letizia et al., 2011, J. Cell Sci. 124(2): 240--251
Regulated Crb accumulation controls apical constriction and invagination in Drosophila tracheal cells. [FBrf0212559]
Müller et al., 2011, Neuron 69(4): 749--762
Rab3-GAP Controls the Progression of Synaptic Homeostasis at a Late Stage of Vesicle Release. [FBrf0213055]
Ohsawa et al., 2011, Dev. Cell 20(3): 315--328
Elimination of Oncogenic Neighbors by JNK-Mediated Engulfment in Drosophila. [FBrf0213219]
Oshima and Fehon, 2011, J. Cell Sci. 124(16): 2861--2871
Analysis of protein dynamics within the septate junction reveals a highly stable core protein complex that does not include the basolateral polarity protein Discs large. [FBrf0214577]
Park et al., 2011, Biochem. Biophys. Res. Commun. 404(2): 638--645
Normal prion protein in Drosophila enhances the toxicity of pathogenic polyglutamine proteins and alters susceptibility to oxidative and autophagy signaling modulators. [FBrf0212784]
Raghu and Borst, 2011, PLoS ONE 6(5): e19472
Candidate glutamatergic neurons in the visual system of Drosophila. [FBrf0213690]
Ribeiro et al., 2011, PLoS Genet. 7(2): e1001295
Phosphoinositide regulation of integrin trafficking required for muscle attachment and maintenance. [FBrf0213137]
Rossetto et al., 2011, Hum. Mol. Genet. 20(21): 4248--4257
Defhc1.1, a homologue of the juvenile myoclonic gene EFHC1, modulates architecture and basal activity of the neuromuscular junction in Drosophila. [FBrf0216330]
Shih and Chiang, 2011, J. Neurogenet. 25(1-2): 1--6
Anatomical Characterization of Thermosensory AC Neurons in the Adult Drosophila Brain. [FBrf0213700]
Syed et al., 2011, J. Neurosci. 31(21): 7876--7885
The CD59 Family Member Leaky/Coiled Is Required for the Establishment of the Blood-Brain Barrier in Drosophila. [FBrf0213741]
Szul et al., 2011, Cell. Logist. 1(2): 69--76
The Garz Sec7 domain guanine nucleotide exchange factor for Arf regulates salivary gland development in Drosophila. [FBrf0213963]
Uytterhoeven et al., 2011, Cell 145(1): 117--132
Loss of skywalker reveals synaptic endosomes as sorting stations for synaptic vesicle proteins. [FBrf0213384]
Varija Raghu et al., 2011, J. Comp. Neurol. 519(1): 162--176
Neurons with cholinergic phenotype in the visual system of Drosophila. [FBrf0212356]
Wang et al., 2011, Dev. Biol. 350(2): 414--428
Notch signaling regulates neuroepithelial stem cell maintenance and neuroblast formation in Drosophila optic lobe development. [FBrf0212909]
Willecke et al., 2011, Oncogene 30(39): 4067--4074
Loss of PI3K blocks cell-cycle progression in a Drosophila tumor model. [FBrf0216281]
Wu et al., 2011, Curr. Biol. 21(10): 848--854
Heterotypic Gap Junctions between Two Neurons in the Drosophila Brain Are Critical for Memory. [FBrf0213804]
Bachmann et al., 2010, J. Neurosci. 30(17): 5811--5824
A perisynaptic ménage à trois between Dlg, DLin-7, and Metro controls proper organization of Drosophila synaptic junctions. [FBrf0210640]
Bahri et al., 2010, Development 137(12): 2023--2032
The leading edge during dorsal closure as a model for epithelial plasticity: Pak is required for recruitment of the Scribble complex and septate junction formation. [FBrf0210918]
Ball et al., 2010, Neuron 66(4): 536--549
Retrograde BMP Signaling Controls Synaptic Growth at the NMJ by Regulating Trio Expression in Motor Neurons. [FBrf0210920]
Banovic et al., 2010, Neuron 66(5): 724--738
Drosophila Neuroligin 1 Promotes Growth and Postsynaptic Differentiation at Glutamatergic Neuromuscular Junctions. [FBrf0211035]
Beam and Moberg, 2010, Fly 4(2): 104--116
The gang of four gene regulates growth and patterning of the developing Drosophila eye. [FBrf0211089]
Buchon et al., 2010, BMC Biol. 8: 152
Drosophila EGFR pathway coordinates stem cell proliferation and gut remodeling following infection. [FBrf0212840]
Cabernard et al., 2010, Nature 467(7311): 91--94
A spindle-independent cleavage furrow positioning pathway. [FBrf0211664]
Campbell et al., 2010, Mech. Dev. 127(7-8): 345--357
Mesenchymal-to-epithelial transition of intercalating cells in Drosophila renal tubules depends on polarity cues from epithelial neighbours. [FBrf0211143]
Chen et al., 2010, PLoS ONE 5(3): e9480
Role of Spastin in Apical Domain Control along the Rhabdomere Elongation in Drosophila Photoreceptor. [FBrf0210148]
Choi et al., 2010, Hum. Mol. Genet. 19(22): 4474--4489
A Drosophila model of GSS syndrome suggests defects in active zones are responsible for pathogenesis of GSS syndrome. [FBrf0212151]
Cordero et al., 2010, Dev. Cell 18(6): 999--1011
Oncogenic Ras diverts a host TNF tumor suppressor activity into tumor promoter. [FBrf0211264]
Ekas et al., 2010, Dev. Biol. 344(2): 621--636
Characterization of a dominant-active STAT that promotes tumorigenesis in Drosophila. [FBrf0211400]
Fan et al., 2010, Cell Death Differ. 17(6): 912--921
Dual roles of Drosophila p53 in cell death and cell differentiation. [FBrf0210741]
Fernandes et al., 2010, Dev. Cell 18(1): 64--76
Zona pellucida domain proteins remodel the apical compartment for localized cell shape changes. [FBrf0211093]
Fichelson et al., 2010, Development 137(5): 815--824
lethal giant larvae is required with the par genes for the early polarization of the Drosophila oocyte. [FBrf0209930]
Forster et al., 2010, Curr. Biol. 20(1): 62--68
Sec24-Dependent Secretion Drives Cell-Autonomous Expansion of Tracheal Tubes in Drosophila. [FBrf0209657]
Franz and Riechmann, 2010, Dev. Biol. 338(2): 136--147
Stepwise polarisation of the Drosophila follicular epithelium. [FBrf0209855]
Garlena et al., 2010, J. Cell Sci. 123(18): 3177--3188
Regulation of mixed-lineage kinase activation in JNK-dependent morphogenesis. [FBrf0211702]
Georgiou and Baum, 2010, J. Cell Sci. 123(7): 1089--1098
Polarity proteins and Rho GTPases cooperate to spatially organise epithelial actin-based protrusions. [FBrf0214990]
Gervais and Casanova, 2010, Curr. Biol. 20(4): 359--366
In Vivo Coupling of Cell Elongation and Lumen Formation in a Single Cell. [FBrf0210105]
Graham et al., 2010, J. Biol. Chem. 285(15): 11143--11153
Neurologic dysfunction and male infertility in Drosophila porin mutants: a new model for mitochondrial dysfunction and disease. [FBrf0210435]
Grzeschik et al., 2010, Curr. Biol. 20(7): 573--581
Lgl, aPKC, and Crumbs regulate the Salvador/Warts/Hippo pathway through two distinct mechanisms. [FBrf0210559]
Haglund et al., 2010, Curr. Biol. 20(10): 944--950
Cindr interacts with anillin to control cytokinesis in Drosophila melanogaster. [FBrf0210868]
Hamanaka and Meinertzhagen, 2010, J. Comp. Neurol. 518(7): 1133--1155
Immunocytochemical localization of synaptic proteins to photoreceptor synapses of Drosophila melanogaster. [FBrf0209968]
Hamel et al., 2010, J. Cell Biol. 188(4): 581--594
Notch ligand activity is modulated by glycosphingolipid membrane composition in Drosophila melanogaster. [FBrf0210025]
Harumoto et al., 2010, Dev. Cell 19(3): 389--401
Atypical cadherins dachsous and fat control dynamics of noncentrosomal microtubules in planar cell polarity. [FBrf0211754]
Ho et al., 2010, Dev. Biol. 337(2): 274--283
Mob as tumor suppressor is activated at the cell membrane to control tissue growth and organ size in Drosophila. [FBrf0209794]
Ho et al., 2010, Development 137(5): 745--754
Echinoid regulates Flamingo endocytosis to control ommatidial rotation in the Drosophila eye. [FBrf0209940]
Januschke and Gonzalez, 2010, J. Cell Biol. 188(5): 693--706
The interphase microtubule aster is a determinant of asymmetric division orientation in Drosophila neuroblasts. [FBrf0210175]
Kaplan and Tolwinski, 2010, J. Cell Sci. 123(18): 3157--3165
Spatially defined Dsh-Lgl interaction contributes to directional tissue morphogenesis. [FBrf0211705]
Khuong et al., 2010, Proc. Natl. Acad. Sci. U.S.A. 107(40): 17379--17384
WASP is activated by phosphatidylinositol-4,5-bisphosphate to restrict synapse growth in a pathway parallel to bone morphogenetic protein signaling. [FBrf0214154]
Kim et al., 2010, J. Asia-Pacific Ent. 13(4): 339--343
Alterations in both acetylcholinesterase activity and synaptic scaffolding protein localization in the nervous system of Drosophila presenilin mutants. [FBrf0212161]
Kim and Marqués, 2010, Dev. Dyn. 239(9): 2413--2425
Identification of downstream targets of the Bone Morphogenetic Protein pathway in the Drosophila nervous system. [FBrf0211763]
Kitajima et al., 2010, Dev. Biol. 347(1): 9--23
Progenitor properties of symmetrically dividing Drosophila neuroblasts during embryonic and larval development. [FBrf0211968]
Krahn et al., 2010, Curr. Biol. 20(7): 636--642
Membrane targeting of Bazooka/PAR-3 is mediated by direct binding to phosphoinositide lipids. [FBrf0210551]
Laplante et al., 2010, Dev. Dyn. 239(9): 2509--2519
Echinoid regulates tracheal morphology and fusion cell fate in Drosophila. [FBrf0211771]
Laprise et al., 2010, Curr. Biol. 20(1): 55--61
Epithelial Polarity Proteins Regulate Drosophila Tracheal Tube Size in Parallel to the Luminal Matrix Pathway. [FBrf0209969]
Lee et al., 2010, J. Neurosci. 30(50): 16959--16969
LRRK2 kinase regulates synaptic morphology through distinct substrates at the presynaptic and postsynaptic compartments of the Drosophila neuromuscular junction. [FBrf0212570]
Lee and Wu, 2010, J. Neurosci. 30(47): 15821--15833
Orchestration of stepwise synaptic growth by k+ and Ca2+ channels in Drosophila. [FBrf0212405]
Levine et al., 2010, Dev. Biol. 344(1): 196--209
Opposing interactions between Drosophila Cut and the C/EBP encoded by Slow Border Cells direct apical constriction and epithelial invagination. [FBrf0211314]
Liu et al., 2010, J. Neurosci. 30(35): 11624--11634
Distinct Presynaptic and Postsynaptic Dismantling Processes of Drosophila Neuromuscular Junctions during Metamorphosis. [FBrf0211694]
Marie et al., 2010, J. Neurosci. 30(24): 8071--8082
Synaptic homeostasis is consolidated by the cell fate gene gooseberry, a Drosophila pax3/7 homolog. [FBrf0211066]
Masuda-Nakagawa et al., 2010, Gene Expr. Patterns 10(7-8): 328--337
Targeting expression to projection neurons that innervate specific mushroom body calyx and antennal lobe glomeruli in larval Drosophila. [FBrf0211879]
Maurel-Zaffran et al., 2010, Dev. Biol. 343(1-2): 18--27
Reiterative use of signalling pathways controls multiple cellular events during Drosophila posterior spiracle organogenesis. [FBrf0211024]
Maynard et al., 2010, Dev. Biol. 339(2): 295--306
Gp93, the Drosophila GRP94 ortholog, is required for gut epithelial homeostasis and nutrient assimilation-coupled growth control. [FBrf0210107]
Milton et al., 2010, Development 137(5): 735--743
Differential requirement of Salvador-Warts-Hippo pathway members for organ size control in Drosophila melanogaster. [FBrf0209966]
Morais-de-Sá et al., 2010, Cell 141(3): 509--523
aPKC phosphorylation of Bazooka defines the apical/lateral border in Drosophila epithelial cells. [FBrf0210663]
Morimoto et al., 2010, Neuroscience 165(4): 1284--1292
Subunit-specific and homeostatic regulation of glutamate receptor localization by CaMKII in Drosophila neuromuscular junctions. [FBrf0209866]
Mosca and Schwarz, 2010, Nat. Neurosci. 13(8): 935--943
The nuclear import of Frizzled2-C by Importins-beta11 and alpha2 promotes postsynaptic development. [FBrf0211361]
Murthy et al., 2010, Development 137(16): 2773--2783
Sec5, a member of the exocyst complex, mediates Drosophila embryo cellularization. [FBrf0211434]
Nahm et al., 2010, J. Neurosci. 30(24): 8138--8150
dCIP4 (Drosophila Cdc42-interacting protein 4) restrains synaptic growth by inhibiting the secretion of the retrograde Glass bottom boat signal. [FBrf0211075]
Nelson et al., 2010, Genetics 185(3): 831--839
The Drosophila Claudin Kune-kune Is Required for Septate Junction Organization and Tracheal Tube Size Control. [FBrf0211332]
Padash-Barmchi et al., 2010, J. Cell Sci. 123(23): 4052--4062
Control of Gliotactin localization and levels by tyrosine phosphorylation and endocytosis is necessary for survival of polarized epithelia. [FBrf0212409]
Robinson et al., 2010, Curr. Biol. 20(7): 582--590
Crumbs regulates Salvador/Warts/Hippo signaling in Drosophila via the FERM-domain protein expanded. [FBrf0210560]
Rohrbough and Broadie, 2010, Development 137(20): 3523--3533
Anterograde Jelly belly ligand to Alk receptor signaling at developing synapses is regulated by Mind the gap. [FBrf0211915]
Sekyrova et al., 2010, Development 137(1): 141--150
Interaction between Drosophila bZIP proteins Atf3 and Jun prevents replacement of epithelial cells during metamorphosis. [FBrf0209550]
Simone and DiNardo, 2010, Development 137(8): 1385--1394
Actomyosin contractility and Discs large contribute to junctional conversion in guiding cell alignment within the Drosophila embryonic epithelium. [FBrf0210407]
Tamori et al., 2010, PLoS Biol. 8(7): e1000422
Involvement of Lgl and Mahjong/VprBP in Cell Competition. [FBrf0211298]
Thomson and Johnson, 2010, Cell Death Differ. 17(11): 1717--1727
Inducible somatic oocyte destruction in response to rapamycin requires wild-type regulation of follicle cell epithelial polarity. [FBrf0211996]
Tikhmyanova et al., 2010, PLoS ONE 5(8): e12369
Dcas supports cell polarization and cell-cell adhesion complexes in development. [FBrf0211678]
Tsurudome et al., 2010, Neuron 68(5): 879--893
The Drosophila miR-310 Cluster Negatively Regulates Synaptic Strength at the Neuromuscular Junction. [FBrf0212495]
Walther and Pichaud, 2010, Curr. Biol. 20(12): 1065--1074
Crumbs/DaPKC-Dependent Apical Exclusion of Bazooka Promotes Photoreceptor Polarity Remodeling. [FBrf0211169]
Warner et al., 2010, Curr. Biol. 20(8): 677--686
The Cdc42/Par6/aPKC Polarity Complex Regulates Apoptosis-Induced Compensatory Proliferation in Epithelia. [FBrf0211164]
Yu et al., 2010, Dev. Cell 18(2): 288--299
Kibra Functions as a Tumor Suppressor Protein that Regulates Hippo Signaling in Conjunction with Merlin and Expanded. [FBrf0210017]
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