A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Gene Dmel\shi

General Information
SymbolDmel\shiSpeciesD. melanogaster
NameshibireAnnotation symbolCG18102
Feature typeprotein_coding_geneFlyBase IDFBgn0003392
Gene Model StatusCurrent Stock availability 30 publicly available
Also Known AsDyn, Ddyn
Genomic Location
Chromosome (arm)XRecombination map1-51.5
Cytogenetic map13F18-13F18Sequence locationX:15,786,149..15,800,285 [+]

Genomic Maps

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Automatically generated summary

See sections below for more information
The gene shibire is referred to in FlyBase by the symbol Dmel\shi (CG18102, FBgn0003392). It is a protein_coding_gene from Drosophila melanogaster. There is experimental evidence that it has the molecular function: actin binding; microtubule binding. There is experimental evidence for 34 unique biological process terms, many of which group under: anatomical structure development; biological regulation; cellular component organization or biogenesis; localization; multicellular organismal reproductive process; regulation of biological process; synaptic transmission; learning; mating; memory; associative learning; cellular process involved in reproduction. 75 alleles are reported. The phenotypes of these alleles are annotated with: organ system subdivision; external compound sense organ; adult segment; peripheral nervous system; nervous system; female germline cyst; antennal segment; late extended germ band embryo; adult mesothoracic segment; muscle founder cell. It has 12 annotated transcripts and 12 annotated polypeptides. Protein features are: Dynamin; Dynamin GTPase effector; Dynamin central domain; Dynamin, GTPase domain; Dynamin, GTPase region, conserved site; GTPase effector domain, GED; Pleckstrin homology domain; Pleckstrin homology-type. 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, at stages throughout the larval period, at stages throughout the pupal period, 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 at high levels in the following post-embryonic organs or tissues: adult eye, adult central nervous system. Expression at moderate levels in the following post-embryonic organs or tissues: adult head, larval central nervous system, larval midgut, larval/adult hindgut, larval Malpighian tubules, adult heart, adult salivary gland, larval trachea, adult testis, larval carcass. Gene sequence location is X:15786149..15800285.

External Summaries
hide Phenotypic Description from the Red Book (Lindsley & Zimm 1992)
Gene/Allele symbols may differ from current usage
shi: shibire (C. A. Poodry)
The shibire locus is characterized by its temperature-sensitive alleles, which are reversibly paralyzed by exposure to 29, but are essentially normal at 22 (Grigliatti et al.). Exposure of developing animals to the restrictive temperature for pulses of one to several hours leads to a plethora of developmental defects, which are specific for the stage treated (Poodry, Hall, and Suzuki, 1973, Dev. Biol. 66: 442-56) (see following table). Short exposures to restrictive temperatures at the time of delamination of the neuroblasts from the neurogenic ectoderm leads to excess neurogenesis at the expense of epidermogenesis, as seen in the neurogenic mutants (Poodry, 1990, Dev. Biol., in press). Differentiation of myoblasts and neuroblasts is inhibited in shi1 embryonic cells in vitro at 30 (Buzin, Dewhurst, and Seecof, 1978, Dev. Biol. 66: 442-56). Embryonic neurons cultured at 30 show reduced adhesion to the substrate, retardation of growth cone formation and suppressed neuron formation and elongation; reversed by shift to permissive temperature (Kim and Wu, 1987, J. Neurosci. 7: 3245-55). Lethal embryos disorganized by the restrictive temperature can be cultured in vivo as tumorous masses (Poodry). Eye-antenna discs can also be cultured as tumorous masses for several transfer generations (Williams, 1981, DIS 56: 158-61). Primary in vivo culture of cut leg imaginal discs leads to an exceptionally high rate of transdetermination (Poodry).
            

temperature-
sensitive period               developmental phenotype
_________________________________________________________________________
1.5-3 hr                       loss of pole cells
3-4 hr                         fusion of cell membranes leading
                               to syncytium
5-12 hr                        disorganized proliferation of cells
                               leading to transplantable tumorous
                               masses
late third instar              stubby legs; joints missing;
  12 hr heat pulse             clipped wings
48 hr before pupariation       eye scar (loss of pigment cells
                               and cone cells).  The later the
                               heat pulse, the more anterior the
                               position of the scar on eye
pupariation to pupation        animals die and fail to undergo
                               pupation
14-24 hr after pupariation     supernumerary microchaetae on head
                               and thorax; the temperature sensitive
                               period for each bristle site precedes
                               the final cell division of bristle
                               precursor; loss of macrochaetae on
                               head and thorax.  Disruption of giant-
                               fiber pathway development (Hummon and
                               Costello, 1987, J. Neurosci. 7:  3633-38).
                               Reduced numbers of dorsal-longitudinal
                               flight muscles (Hummon and Costello,
                               1988, Roux's Arch. Dev. Biol.
                               197:  383-93)
24-36 hr after pupariation     loss of head and thoracic micro-
                               chaetae; supernumerary abdominal
                               macrochaetae and microchaetae
28-42 hr after pupariation     loss of abdominal macrochaetae
                               and microchaetae
32-48 hr after pupariation     loss of abdominal microchaetae
48 hr after pupariation        scimitar-shaped bristles
adult                          eggs fail to mature

            
            
The temperature-sensitive alleles differ in the severity of their paralysis, recovery period, the restrictive temperature for developmental effects, and in their viability as hemizygotes. They are all hypomorphs, being recessive and having a more extreme expression in combination with a deficiency than when homozygous. A wild-type paternal gene can rescue an egg from a homozygous mother only after 10 hr of development (Swanson and Poodry, 1976, Dev. Biol. 48: 205-11). Of the developmental effects tested, all are autonomous in mosaics generated by somatic recombination or in gynandromorphs (Poodry). The developmental effects on bristles is not enhanced or suppressed by the presence of temperature-sensitive alleles of N; shi is epistatic to N (Lujan, 1981, DIS 56: 86). Physiological studies of shi have revealed the loss of transients in electroretinograms (Kelley and Suzuki, 1974, Proc. Nat. Acad. Sci. USA 71: 4906-09) and failure of neuromuscular transmission at the restrictive temperature (Ikeda, Ozawa, and Hagiwara, 1976, Nature 259: 489-91; Siddiqi and Benzer, 1976, Proc Nat. Acad. Sci. USA 73: 3253-57), though axonal conduction and muscle membrane excitability are unimpaired (Ikeda et al.). Exposure of shi1 adults to 29 causes the depletion of synaptic vesicles from the neuromuscular synapse and their replacement with large cisternae (Poodry and Edgar, 1979, J. Cell Biol. 81: 520-27; Koenig, Saito, and Ikeda, 1983, J. Cell Biol. 96: 1517-22). Accumulation of acetyl choline is reduced at the restrictive temperature, not because of reduced synthesis but because of an abnormally rapid rate of release from the cell, which is not reduced by inhibiting tetrodotoxin-sensitive nerve activity (Wu, Merneking, and Barker, 1983, J. Neurochem. 40: 1386-96). Endocytosis is reversibly blocked in the nerve terminus (Kosaka and Ikeda, 1983, Neurobiol. 14: 207-25; Masur, Kim, and Wu, 1990, J. Neurosci.) and may limit the ability of nerves to regenerate synaptic vesicles. Neuromuscular transmission temperature is sensitive in mosaics in which the neuron but not the muscle is mutant, but not in the converse situation (Koenig and Ikeda, 1983, J. Neurobiol. 14: 411-19). During recovery from exposure to 30 shits1 muscles display a multimodal distribution of miniature excitatory junction potential amplitudes never seen in wild type (Ikeda and Koenig, 1987, J. Physiol. 406: 215-23). Further, as the temperature is increased the amplitude of evoked excitatory junction potentials decreases; the numbers of vesicles per synapse displays a correlated decrease (Koenig, Kosaka, and Ikeda, 1989, J. Neurosci. 9: 1937-42). Endocytosis is also blocked in the garland cells (Kosaka and Ikeda, 1983, J. Cell Biol. 97: 499-507). Vesiculation of cell membranes results in fusion of blastoderm cells (Swanson and Poodry, 1981, Dev. Biol. 84: 465-70) and vesiculation of surface membranes accompanies secretion of protein epicuticle (Poodry).
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Description
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FB2011_10
FB2012_01
Sequence features
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
13F18-13F18  
Limits computationally determined from genome sequence between P{EP}Gβ13FEP1071 and P{EP}EP1458&P{EP}EP1522  
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
13F-14A  
(determined by in situ hybridisation)  
14A-14A  
(determined by in situ hybridisation)  
13F16-14A1  
(determined by in situ hybridisation)  
14A-14A  
Determined by comparing Celera genomic sequence with sequence from BDGP BAC and P1 clones.  
Experimentally Determined Recombination Data
Location
1-51.5
 
Left of (cM)
Right of (cM)
Notes
hide Gene Model & Products
Please see the GBrowse view of Dmel\shi for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
detailed view FBtr0301598 FBtr0074117 FBtr0074121 FBtr0074124 FBtr0074123 FBtr0074122 FBtr0074118 FBtr0301594 FBtr0301597 FBtr0111036 FBtr0301595 FBtr0111037 FBtr0074119 FBtr0301596 FBtr0300392 FBtr0300391 FBtr0300393 FBpp0073927 FBpp0290810 FBpp0110335 FBpp0290811 FBpp0110336 FBpp0073929 FBpp0089277 FBpp0290812 FBpp0089279 FBpp0089280 FBpp0089278 FBpp0073928 FBpp0290809 FBpp0289621 FBpp0289620 FBpp0289622 FBti0021212 FBti0071282
Comments on Gene Model
EST data suggest additional 5' exon(s)
hide Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Associated CDS (aa)
FBtr0074121
  4151
  830
FBtr0074118
  4341
  830
FBtr0074119
  4039
  830
FBtr0074122
  4169
  830
FBtr0074123
  3208
  877
FBtr0074124
  3190
  877
FBtr0111036
  4469
  830
FBtr0111037
  4441
  830
FBtr0301594
  3380
  877
FBtr0301595
  3275
  877
FBtr0301596
  3096
  883
FBtr0301597
  4359
  836
Additional Transcript Data & Comments
Reported size (kB)
5.1, 4.3 (northern blot)
Comments
External Data
Crossreferences
hide Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
RefSeq ID
GenBank protein
shi-PA  
FBpp0089278  
93.0  
830  
8.43  
shi-PB  
FBpp0073928  
93.0  
830  
8.43  
shi-PC  
FBpp0073929  
93.0  
830  
8.43  
shi-PE  
FBpp0089279  
93.0  
830  
8.43  
shi-PF  
FBpp0089280  
97.8  
877  
8.58  
shi-PG  
FBpp0089277  
97.8  
877  
8.58  
shi-PH  
FBpp0110335  
93.0  
830  
8.43  
shi-PI  
FBpp0110336  
93.0  
830  
8.43  
shi-PJ  
FBpp0290809  
97.8  
877  
8.58  
shi-PK  
FBpp0290810  
97.8  
877  
8.58  
shi-PL  
FBpp0290811  
98.5  
883  
8.43  
shi-PM  
FBpp0290812  
93.7  
836  
8.26  
Additional Polypeptide Data & Comments
Reported size (kDa)
883, 836 (aa); 100 (kD observed)
Comments
A form of shi protein which localizes predominantly to the head. This form includes 6aa inserted at the first alternate splice site (Alt1) that are absent in the "body" form of the protein.
A form of shi protein which localizes predominantly to the body. This form lacks 6aa inserted at the first alternate splice site (Alt1) that are present in the "head" form of the protein. An antibody to shi was generated in mouse that reacts primarily with the body form of shi protein. This difference supports the existence of different brain and body forms but the differential immunoreactivity could not be completely explained by the splicing variants identified here.
alternative 3' exon
External Data
Linkouts
Crossreferences
InterPro domains - A database of protein families, domains, and functional sites
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
No Assay Recorded
Stage
Tissue/Position (including subcellular localization)
Reference
dissected tissue
Stage
Tissue/Position (including subcellular localization)
Reference
in situ
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data
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
western blot
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data
Marker for
Subcellular Localization
CV Term
Notes
hide High-Throughput Expression Data
or
Untitled Document detailed view CG15916-RA shi-RA shi-RG shi-RF shi-RE shi-RB shi-RJ shi-RM shi-RH shi-RK shi-RI shi-RC shi-RL CycD-RE CycD-RD CycD-RF
See Gelbart and Emmert, 2010.10.13 for analysis details and data files for all genes.

modENCODE Temporal Expression Data for FBgn0003392


   Styles
Linear
Logarithmic
Heatmap
   Scales
max expr for FBgn0003392
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, at stages throughout the larval period, at stages throughout the pupal period, 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 FBgn0003392 expression level
Developmental Stage   Expression Level
embryo 00-02hr
 
 2479
embryo 02-04hr
 
 2573
embryo 04-06hr
 
 1368
embryo 06-08hr
 
 1382
embryo 08-10hr
 
 1881
embryo 10-12hr
 
 1802
embryo 12-14hr
 
 2445
embryo 14-16hr
 
 3062
embryo 16-18hr
 
 3666
embryo 18-20hr
 
 3429
embryo 20-22hr
 
 3178
embryo 22-24hr
 
 3778
larva L1
 
 2784
larva L2
 
 1557
larva L3 12hr old
 
 1053
larva L3 puffstage 1-2
 
 1051
larva L3 puffstage 3-6
 
 1735
larva L3 puffstage 7-9
 
 2190
white prepupae new
 
 2415
white prepupae 12hr
 
 2187
white prepupae 24hr
 
 2657
pupae 2d postWPP
 
 2944
pupae 3d postWPP
 
 3778
pupae 4d postWPP
 
 2936
adult male 01day
 
 3352
adult male 05day
 
 3439
adult male 30day
 
 3149
adult female 01day
 
 2264
adult female 05day
 
 2319
adult female 30day
 
 2127
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
 High 
Linear, scaled to Very low expression
Developmental Stage   Expression Level
embryo 00-02hr
 (2479)
embryo 02-04hr
 (2573)
embryo 04-06hr
 (1368)
embryo 06-08hr
 (1382)
embryo 08-10hr
 (1881)
embryo 10-12hr
 (1802)
embryo 12-14hr
 (2445)
embryo 14-16hr
 (3062)
embryo 16-18hr
 (3666)
embryo 18-20hr
 (3429)
embryo 20-22hr
 (3178)
embryo 22-24hr
 (3778)
larva L1
 (2784)
larva L2
 (1557)
larva L3 12hr old
 (1053)
larva L3 puffstage 1-2
 (1051)
larva L3 puffstage 3-6
 (1735)
larva L3 puffstage 7-9
 (2190)
white prepupae new
 (2415)
white prepupae 12hr
 (2187)
white prepupae 24hr
 (2657)
pupae 2d postWPP
 (2944)
pupae 3d postWPP
 (3778)
pupae 4d postWPP
 (2936)
adult male 01day
 (3352)
adult male 05day
 (3439)
adult male 30day
 (3149)
adult female 01day
 (2264)
adult female 05day
 (2319)
adult female 30day
 (2127)
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
Linear, scaled to Moderate expression
Developmental Stage   Expression Level
embryo 00-02hr
 (2479)
embryo 02-04hr
 (2573)
embryo 04-06hr
 
 1368
embryo 06-08hr
 
 1382
embryo 08-10hr
 (1881)
embryo 10-12hr
 (1802)
embryo 12-14hr
 (2445)
embryo 14-16hr
 (3062)
embryo 16-18hr
 (3666)
embryo 18-20hr
 (3429)
embryo 20-22hr
 (3178)
embryo 22-24hr
 (3778)
larva L1
 (2784)
larva L2
 (1557)
larva L3 12hr old
 
 1053
larva L3 puffstage 1-2
 
 1051
larva L3 puffstage 3-6
 (1735)
larva L3 puffstage 7-9
 (2190)
white prepupae new
 (2415)
white prepupae 12hr
 (2187)
white prepupae 24hr
 (2657)
pupae 2d postWPP
 (2944)
pupae 3d postWPP
 (3778)
pupae 4d postWPP
 (2936)
adult male 01day
 (3352)
adult male 05day
 (3439)
adult male 30day
 (3149)
adult female 01day
 (2264)
adult female 05day
 (2319)
adult female 30day
 (2127)
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
Linear, scaled to High expression
Developmental Stage   Expression Level
embryo 00-02hr
 
 2479
embryo 02-04hr
 
 2573
embryo 04-06hr
 
 1368
embryo 06-08hr
 
 1382
embryo 08-10hr
 
 1881
embryo 10-12hr
 
 1802
embryo 12-14hr
 
 2445
embryo 14-16hr
 
 3062
embryo 16-18hr
 
 3666
embryo 18-20hr
 
 3429
embryo 20-22hr
 
 3178
embryo 22-24hr
 
 3778
larva L1
 
 2784
larva L2
 
 1557
larva L3 12hr old
 
 1053
larva L3 puffstage 1-2
 
 1051
larva L3 puffstage 3-6
 
 1735
larva L3 puffstage 7-9
 
 2190
white prepupae new
 
 2415
white prepupae 12hr
 
 2187
white prepupae 24hr
 
 2657
pupae 2d postWPP
 
 2944
pupae 3d postWPP
 
 3778
pupae 4d postWPP
 
 2936
adult male 01day
 
 3352
adult male 05day
 
 3439
adult male 30day
 
 3149
adult female 01day
 
 2264
adult female 05day
 
 2319
adult female 30day
 
 2127
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
 
 2479
embryo 02-04hr
 
 2573
embryo 04-06hr
 
 1368
embryo 06-08hr
 
 1382
embryo 08-10hr
 
 1881
embryo 10-12hr
 
 1802
embryo 12-14hr
 
 2445
embryo 14-16hr
 
 3062
embryo 16-18hr
 
 3666
embryo 18-20hr
 
 3429
embryo 20-22hr
 
 3178
embryo 22-24hr
 
 3778
larva L1
 
 2784
larva L2
 
 1557
larva L3 12hr old
 
 1053
larva L3 puffstage 1-2
 
 1051
larva L3 puffstage 3-6
 
 1735
larva L3 puffstage 7-9
 
 2190
white prepupae new
 
 2415
white prepupae 12hr
 
 2187
white prepupae 24hr
 
 2657
pupae 2d postWPP
 
 2944
pupae 3d postWPP
 
 3778
pupae 4d postWPP
 
 2936
adult male 01day
 
 3352
adult male 05day
 
 3439
adult male 30day
 
 3149
adult female 01day
 
 2264
adult female 05day
 
 2319
adult female 30day
 
 2127
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
 High 
 Very high 
 Extremely high 
log, scaled to maximum FBgn0003392 expression level
Developmental Stage   Expression Level
embryo 00-02hr
 
 2479
embryo 02-04hr
 
 2573
embryo 04-06hr
 
 1368
embryo 06-08hr
 
 1382
embryo 08-10hr
 
 1881
embryo 10-12hr
 
 1802
embryo 12-14hr
 
 2445
embryo 14-16hr
 
 3062
embryo 16-18hr
 
 3666
embryo 18-20hr
 
 3429
embryo 20-22hr
 
 3178
embryo 22-24hr
 
 3778
larva L1
 
 2784
larva L2
 
 1557
larva L3 12hr old
 
 1053
larva L3 puffstage 1-2
 
 1051
larva L3 puffstage 3-6
 
 1735
larva L3 puffstage 7-9
 
 2190
white prepupae new
 
 2415
white prepupae 12hr
 
 2187
white prepupae 24hr
 
 2657
pupae 2d postWPP
 
 2944
pupae 3d postWPP
 
 3778
pupae 4d postWPP
 
 2936
adult male 01day
 
 3352
adult male 05day
 
 3439
adult male 30day
 
 3149
adult female 01day
 
 2264
adult female 05day
 
 2319
adult female 30day
 
 2127
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
 (2479)
embryo 02-04hr
 (2573)
embryo 04-06hr
 (1368)
embryo 06-08hr
 (1382)
embryo 08-10hr
 (1881)
embryo 10-12hr
 (1802)
embryo 12-14hr
 (2445)
embryo 14-16hr
 (3062)
embryo 16-18hr
 (3666)
embryo 18-20hr
 (3429)
embryo 20-22hr
 (3178)
embryo 22-24hr
 (3778)
larva L1
 (2784)
larva L2
 (1557)
larva L3 12hr old
 (1053)
larva L3 puffstage 1-2
 (1051)
larva L3 puffstage 3-6
 (1735)
larva L3 puffstage 7-9
 (2190)
white prepupae new
 (2415)
white prepupae 12hr
 (2187)
white prepupae 24hr
 (2657)
pupae 2d postWPP
 (2944)
pupae 3d postWPP
 (3778)
pupae 4d postWPP
 (2936)
adult male 01day
 (3352)
adult male 05day
 (3439)
adult male 30day
 (3149)
adult female 01day
 (2264)
adult female 05day
 (2319)
adult female 30day
 (2127)
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
log, scaled to Moderate expression
Developmental Stage   Expression Level
embryo 00-02hr
 (2479)
embryo 02-04hr
 (2573)
embryo 04-06hr
 
 1368
embryo 06-08hr
 
 1382
embryo 08-10hr
 1881
embryo 10-12hr
 1802
embryo 12-14hr
 2445
embryo 14-16hr
 (3062)
embryo 16-18hr
 (3666)
embryo 18-20hr
 (3429)
embryo 20-22hr
 (3178)
embryo 22-24hr
 (3778)
larva L1
 (2784)
larva L2
 1557
larva L3 12hr old
 
 1053
larva L3 puffstage 1-2
 
 1051
larva L3 puffstage 3-6
 1735
larva L3 puffstage 7-9
 2190
white prepupae new
 2415
white prepupae 12hr
 2187
white prepupae 24hr
 (2657)
pupae 2d postWPP
 (2944)
pupae 3d postWPP
 (3778)
pupae 4d postWPP
 (2936)
adult male 01day
 (3352)
adult male 05day
 (3439)
adult male 30day
 (3149)
adult female 01day
 2264
adult female 05day
 2319
adult female 30day
 2127
Expression Level Scale
 None 
 Extremely low 
 Very low 
 Low 
 Moderate 
 Moderately high 
log, scaled to High expression
Developmental Stage   Expression Level
embryo 00-02hr
 
 2479
embryo 02-04hr
 
 2573
embryo 04-06hr
 
 1368
embryo 06-08hr
 
 1382
embryo 08-10hr
 
 1881
embryo 10-12hr
 
 1802
embryo 12-14hr
 
 2445
embryo 14-16hr
 
 3062
embryo 16-18hr
 
 3666
embryo 18-20hr
 
 3429
embryo 20-22hr
 
 3178
embryo 22-24hr
 
 3778
larva L1
 
 2784
larva L2
 
 1557
larva L3 12hr old
 
 1053
larva L3 puffstage 1-2
 
 1051
larva L3 puffstage 3-6
 
 1735
larva L3 puffstage 7-9
 
 2190
white prepupae new
 
 2415
white prepupae 12hr
 
 2187
white prepupae 24hr
 
 2657
pupae 2d postWPP
 
 2944
pupae 3d postWPP
 
 3778
pupae 4d postWPP
 
 2936
adult male 01day
 
 3352
adult male 05day
 
 3439
adult male 30day
 
 3149
adult female 01day
 
 2264
adult female 05day
 
 2319
adult female 30day
 
 2127
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
 
 2479
embryo 02-04hr
 
 2573
embryo 04-06hr
 
 1368
embryo 06-08hr
 
 1382
embryo 08-10hr
 
 1881
embryo 10-12hr
 
 1802
embryo 12-14hr
 
 2445
embryo 14-16hr
 
 3062
embryo 16-18hr
 
 3666
embryo 18-20hr
 
 3429
embryo 20-22hr
 
 3178
embryo 22-24hr
 
 3778
larva L1
 
 2784
larva L2
 
 1557
larva L3 12hr old
 
 1053
larva L3 puffstage 1-2
 
 1051
larva L3 puffstage 3-6
 
 1735
larva L3 puffstage 7-9
 
 2190
white prepupae new
 
 2415
white prepupae 12hr
 
 2187
white prepupae 24hr
 
 2657
pupae 2d postWPP
 
 2944
pupae 3d postWPP
 
 3778
pupae 4d postWPP
 
 2936
adult male 01day
 
 3352
adult male 05day
 
 3439
adult male 30day
 
 3149
adult female 01day
 
 2264
adult female 05day
 
 2319
adult female 30day
 
 2127
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 FBgn0003392


   Styles
Linear
Logarithmic
Heatmap
Back-to-back
   Scales
max expr for FBgn0003392
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 at high levels in the following post-embryonic organs or tissues: adult eye, adult central nervous system. Expression at moderate levels in the following post-embryonic organs or tissues: adult head, larval central nervous system, larval midgut, larval/adult hindgut, larval Malpighian tubules, adult heart, adult salivary gland, larval trachea, adult testis, larval 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
hide External Data & Images
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
abdominal 2 ventral longitudinal muscle & larval somatic muscle | conditional ts
actin filament & spermatid | conditional ts
adherens junction & wing cell | pupal stage | conditional - heat sensitive
axon & eye photoreceptor cell | conditional - heat sensitive, with Scer\GAL4GMR.PF
eye photoreceptor cell & ommatidium | ectopic
garland cell & endosome
glial cell & brain & pupa | conditional ts, with Scer\GAL4repo
larval somatic muscle & presynaptic membrane | conditional ts
larval somatic muscle & synaptic vesicle | conditional ts
macrochaeta & thorax | conditional ts
mesothoracic tergum & macrochaeta
microchaeta & thorax | conditional ts
photoreceptor cell & synaptic vesicle
wing & macrochaeta
hide Classical Alleles ( 58 )
For All Classical Alleles Show

Allele of shiClassMutagenStocksKnown lesion
shi111 Yes
shi22 Yes
shiKG036902 --
shi100 --
shi110 --
shi12.12Bloss of function allele0 --
shi120 --
shi130 --
shi140 --
shi150 --
shi160 Yes
shi170 --
shi180 --
shi190 Yes
shi200 Yes
shi21loss of function allele0 Yes
shi220 --
shi30 --
shi40 Yes
shi50 --
shi60 --
shi70 --
shi80 --
shi90 --
shiBA10 --
shiBS1
0 --
shiCK2
0 --
shiEM140 --
shiEM180 Yes
shiEM270 --
shiEM330 Yes
shiEM350 Yes
shiEM380 --
shiEM420 Yes
shiEM440 --
shiEM45
0 --
shiEM530 --
shiEM550 --
shiEM560 Yes
shiEM590 --
shiEM610 --
shiEM620 --
shiEM650 --
shiEM660 Yes
shiEM70 --
shiEP-866
0 Yes
shiFL54loss of function allele0 Yes
shiKVS0 Yes
shiSHY0 Yes
shiSK20 --
shitp12
0 --
shitp1
0 --
shitp2
0 --
shitp4
0 --
shitp9
0 --
shiunspecified
0 --
shiVF30 --
shiVS20 Yes
hide Alleles Carried on Transgenic Constructs ( 17 )
For All Alleles Carried on Transgenic Constructs Show

Allele of shiClassMutagenStocksKnown lesion
shiK44A.Scer\UAS4 Yes
shits1.Ncra\QUAS4 Yes
shiGD15292 Yes
shiK39A.GMR2 Yes
shiJF031331 Yes
shiKK1014441 Yes
shits1.Scer\FRT.Ncra\QUAS1 Yes
shi1.Scer\UAS0 Yes
shiK44A.ro0 Yes
shiScer\UAS.cSa0 Yes
shit150 Yes
shits.Scer\FRT.stop.Scer\UAS0 Yes
shits.Scer\UAS.cUa0 Yes
shits.Scer\UAS0 Yes
shits1.-FRT.Ncra\QUAS0 Yes
shits1.Ecol\lexAop0 Yes
shiWT.GMR0 Yes
hide Aneuploid Aberrations
Duplicated in
Disrupted in
Not duplicated in
Not disrupted in
hide Transgenic Constructs & Insertions
Transgenic Constructs
Type of construct
Name
Expression data
Insertions
Type of insertions
Name
Expression data
miscellaneous insertions
insertion of mobile activating element
hide Gene Ontology: Function, Process & Cellular Component ( 47 unique terms )
hide Terms Based on Experimental Evidence ( 39 terms )
Molecular Function
CV term
References
inferred from direct assay
inferred from direct assay
Biological Process
CV term
References
inferred from mutant phenotype
inferred from mutant phenotype
inferred from direct assay
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from direct assay
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from genetic interaction with jar
inferred from mutant phenotype
Cellular Component
CV term
References
inferred from mutant phenotype
hide Terms Based on Predictions or Assertions ( 14 terms )
Molecular Function
CV term
References
inferred from sequence or structural similarity with mouse Dnm
non-traceable author statement
Biological Process
CV term
References
traceable author statement
non-traceable author statement
traceable author statement
traceable author statement
traceable author statement
Cellular Component
CV term
References
inferred from sequence or structural similarity with UniProtKB:P39055
hide Sequence Ontology: Class of Gene
hide Interactions & Pathways
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
shi allele
Gene
References
hide External Data
Linkouts
BioGRID - A database of protein and genetic interactions
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
OrthoDB (Arthropod subset) The hierarchical catalog of eukaryotic orthologs.
hide Stocks & Reagents
hide Stocks Listed in FlyBase ( 30 )
Bloomington
2248
Kyoto
106278
106754
VDRC
hide Genomic Clones ( 2 )
Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete
hide cDNA Clones ( 229 )
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
hide RNAi & Array Information
Linkouts
DRSC - Results from RNAi screens.
GenomeRNAi - GenomeRNAi – A database for cell-based and in vivo RNAi phenotypes and reagents
hide Antibody Information
polyclonal
hide Other Information
hide Discoverer
Grigliatti, 1971.
 
hide Etymology
"shibire" means "paralysed" in Japanese.
hide Identification
hide Relationship to Other Genes
Source for database identity of
Source for database merge of
Source for merge of: shi anon-WO0153538.12 anon-WO0153538.13 anon-WO0153538.14
Source for merge of: shi CG18102
Additional comments
Source for merge of shi anon-WO0153538.12 anon-WO0153538.13 anon-WO0153538.14 was sequence comparison (date:051113).
hide Other Comments
dsRNA made from templates generated with primers directed against shi profoundly promotes the wg-signaling pathway.
RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a phenotype when assayed in Kc167 and S2R+ cells: binucleate cells.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
Dl is not endocytosed in shi mutants.
shi dependent retrieval of secreted sog protein is required for formation of the sog protein gradient across the dorsal side of the blastoderm embryo.
A P{UAS-shits1.K} transgene has been used to show that synaptic transmission from mushroom body neurons is required during memory retrieval but not during acquisition or storage.
shi has a role in maintaining normal heart function.
shi mutants have been used to show that there are two functionally and topographically distinct pools of synaptic vesicles, exo/endo cycling and reserve pools.
Fluorescent Ca-sensitive dye, Ca Crimson, is used to monitor presynaptic Ca dynamics.
In presynaptic terminals α-Adaptin defines a network-like membrane structure to which the GTPase dynamin is recruited. α-Adaptin is necessary for the formation of clathrin coated pits and participates in the dynamin-dependent release of coated vesicles from the membrane surface. Results suggest an α-Adaptin-dependent control of the vesicle cycle that maintains the balance between the amount of vesicle- and surface-associated membranes.
Overexpression of different constitutively active forms of N in shi mutant flies indicates that shi function is not necessary for transduction of the signal downstream of N, even when the receptor, N, is integrated in the plasma membrane. When wild-type N is activated by its ligand Dl, shi is required in both signaling and receiving cells for normal singling out of precursors.
The structure of the protein encoded by the second, stnB ORF suggests a possible role in membrane trafficking, allowing an interpretation of the interaction seen between the various 'stoned' and shi mutants.
The two isoforms of dynamin detected in wild type and shi mutants are associated with two different pellet fractions of head homogenates. At least one isoform is membrane-associated. Normal distribution of dynamin is not affected by heat shock, block of the GTP cycle or the presence of stabilised microtubules in wild type or shi mutants. Results suggest the two isoforms are likely to be involved in separate cellular compartments rather than different functional states in the same membrane-cycling pathway.
Recycling of synaptic vesicle proteins is blocked in temperature sensitive mutants of shi. Similar inhibition of dye uptake is also seen. Vesicle recycling after the block can occur in the absence of extracellular calcium. BWSV induces calcium-independent exocytosis at nerve terminals. It is most likely that calcium is required for the endocytic recycling of synaptic vesicles.
shi gene product is thought to provide the motor for vesicular transport during endocytosis.
Mosaic analysis within muscles demonstrates the developmental focus of the shi mutant phenotype is the muscle itself. The normal shi function, endocytosis, is essential in muscle tissue during a sensitive stage of myogenesis in early pupae.
Mutations at stnA show allele-specific interactions with mutations at dnc and shi. A suppressor of stnA, Su(stn) has been identified. The stnA gene product interacts directly or indirectly with the cAMP second messenger system, synaptic membrane recycling pathway and with biogenic amine metabolism.
Expression of shi is particularly high in CNS and PNS throughout neuronal development.
The shi locus encodes Drosophila dynamin.
shi has been cloned and sequenced.
Studies of the neuromuscular junctions of heat-treated shi1 flies indicate that paralysis is associated with loss of synaptic vesicles. Examination of the neurogenic region of the embryos reveals numerous packets of extracellular vesicles and coated pits blocked in endocytosis.
The shibire locus is characterized by its temperature-sensitive alleles, which are reversibly paralyzed by exposure to 29oC, but are essentially normal at 22oC (Grigliatti, Hall, Rosenbluth and Suzuki, 1973). Exposure of developing animals to the restrictive temperature for pulses of one to several hours leads to a plethora of developmental defects, which are specific for the stage treated (Poodry, Hall and Suzuki, 1973) (see shi1 allele record. Short exposures to restrictive temperatures at the time of delamination of the neuroblasts from the neurogenic ectoderm leads to excess neurogenesis at the expense of epidermogenesis, as seen in the neurogenic mutants (Poodry, 1990). Differentiation of myoblasts and neuroblasts is inhibited in shi1 embryonic cells in vitro at 30oC (Buzin, Dewhurst and Seecof, 1978). Embryonic neurons cultured at 30oC show reduced adhesion to the substrate, retardation of growth cone formation and suppressed neuron formation and elongation; reversed by shift to permissive temperature (Kim and Wu, 1987). Lethal embryos disorganized by the restrictive temperature can be cultured in vivo as tumorous masses (Poodry). Eye-antenna discs can also be cultured as tumorous masses for several transfer generations (Williams, 1981). Primary in vivo culture of cut leg imaginal discs leads to an exceptionally high rate of transdetermination (Poodry). The temperature-sensitive alleles differ in the severity of their paralysis, recovery period, the restrictive temperature for developmental effects and in their viability as hemizygotes. They are all hypomorphs, being recessive and having a more extreme expression in combination with a deficiency than when homozygous. A wild-type paternal gene can rescue an egg from a homozygous mother only after 10 hr of development (Swanson and Poodry, 1976). Of the developmental effects tested, all are autonomous in mosaics generated by somatic recombination or in gynandromorphs (Poodry). The developmental effects on bristles is not enhanced or suppressed by the presence of temperature-sensitive alleles of N; shi is epistatic to N (Lujan, 1981). Physiological studies of shi have revealed the loss of transients in electroretinograms (Kelley and Suzuki, 1974) and failure of neuromuscular transmission at the restrictive temperature (Ikeda, Ozawa and Hagiwara, 1976; Siddiqi and Benzer, 1976), though axonal conduction and muscle membrane excitability are unimpaired (Ikeda, Ozawa and Hagiwara, 1976). Exposure of shi1 adults to 29oC causes the depletion of synaptic vesicles from the neuromuscular synapse and their replacement with large cisternae (Poodry and Edgar, 1979; Koenig, Saito and Ikeda, 1983). Accumulation of acetyl choline is reduced at the restrictive temperature, not because of reduced synthesis but because of an abnormally rapid rate of release from the cell, which is not reduced by inhibiting tetrodotoxin-sensitive nerve activity (Wu, Merneking and Barker, 1983). Endocytosis is reversibly blocked in the nerve terminus (Kosaka and Ikeda, 1983a; Masur, Kim and Wu, 1990) and may limit the ability of nerves to regenerate synaptic vesicles. Neuromuscular transmission temperature is sensitive in mosaics in which the neuron but not the muscle is mutant, but not in the converse situation (Koenig and Ikeda, 1983b). During recovery from exposure to 30oC shi1 muscles display a multimodal distribution of miniature excitatory junction potential amplitudes never seen in wild type (Ikeda and Koenig, 1987). Further, as the temperature is increased the amplitude of evoked excitatory junction potentials decreases; the numbers of vesicles per synapse displays a correlated decrease (Koenig, Kosaka and Ikeda, 1989). Endocytosis is also blocked in the garland cells (Kosaka and Ikeda, 1983a). Vesiculation of cell membranes results in fusion of blastoderm cells (Swanson and Poodry, 1981) and vesiculation of surface membranes accompanies secretion of protein epicuticle (Poodry).
 
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
Linkouts
BioGRID - A database of protein and genetic interactions
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
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 ( 21 )
Reported As
Symbol Synonym
anon-WO0153538.12
 
anon-WO0153538.13
 
anon-WO0153538.14
 
l(1)shi
l(1)VII
 
shi
(Klose et al., 2005, Keene et al., 2004, Mathew et al., 2005, Mathew et al., 2005, Pitman et al., 2006, Bokel et al., 2006, Rives et al., 2006, Keene et al., 2006, Kitamoto, 2002, Narayanan et al., 2005, Dickman, 2006, Ohyama et al., 2007, Baker et al., 2007, Davis, 2004, Gallet et al., 2006, Kicheva et al., 2007, Jekely et al., 2005, Zhao et al., 2008, Acevedo et al., 2007, Mateus et al., 2011, Kitamoto, 2002, Quinones et al., 2010, Hughes and Thomas, 2007, Lee et al., 2008, Trotta et al., 2004, Benhra et al., 2010, Classen et al., 2005, Shiraiwa, 2008, Poodry, 1980, Sasaki et al., 2007, Honjo and Furukubo-Tokunaga, 2005, Ghosh-Roy et al., 2005, Roegiers et al., 2005, Rogat and Miller, 2002, Pinal and Pichaud, 2011, Yuva-Aydemir et al., 2011, Zhang et al., 2008, Barnes et al., 2008, Zhang et al., 2007, Seto and Bellen, 2006, Kvitsiani and Dickson, 2006, Wang et al., 2004, Honjo et al., 2008, Windler and Bilder, 2008, Pai et al., 2006, Molnar et al., 2006, Bakal et al., 2007, Dietzl et al., 2007, Dubnau et al., 2003, Kawasaki et al., 2000, Huang et al., 2006, Hennig et al., 2006, van Swinderen and Greenspan, 2003, Meyer et al., 2006, Kitamoto, 2001, Stewart et al., 2002, Estes et al., 2000, Chen et al., 2002, Robertson et al., 2000, Song et al., 2007, Nallamothu et al., 2008, Pirraglia et al., 2006, Callejo et al., 2006, Han et al., 2007, Tsarouhas et al., 2007, Belenkaya et al., 2008, Sokac and Wieschaus, 2008, Raghu et al., 2009, Chang et al., 2008, Callejo et al., 2008, O'Connor-Giles et al., 2008, Guha et al., 2003, Hoyer et al., 2008, Xia and Tully, 2007, Cronin et al., 2004, Sakai and Kitamoto, 2006, Rister and Heisenberg, 2006, Seugnet et al., 2008, Georgiou et al., 2008, Leibfried et al., 2008, Honjo and Furukubo-Tokunaga, 2009, Loevenich et al., 2009, Nikolaev et al., 2009, Séjourné et al., 2011, Gerber et al., 2004, Su et al., 2007, Yang et al., 2009, Häsemeyer et al., 2009, Doherty et al., 2009, Zimmermann et al., 2009, Kilman et al., 2009, Pouille et al., 2009, Xu et al., 2008, Desai et al., 2009, Sousa-Nunes et al., 2011, Hall, 2003, Kumar et al., 2009, Verstreken et al., 2005, van Swinderen et al., 2009, Soukup et al., 2009, Peralta et al., 2009, Sakai et al., 2009, Beramendi et al., 2007, Thum et al., 2006, Yan et al., 2009, Joseph et al., 2009, Li et al., 2010, Katsuki et al., 2009, Krashes et al., 2009, Hsouna et al., 2007, Venken et al., 2009, Yao et al., 2009, Huntwork and Littleton, 2007, Gonzalez-Bellido et al., 2009, Zhou et al., 2008, Gao et al., 2008, Krashes et al., 2007, Cherry and Perrimon, 2004, Schwaerzel et al., 2002, Rohrbough and Broadie, 2002, Koenig and Ikeda, 2005, Wu et al., 2005, Koenig and Ikeda, 2007, Gao et al., 2008, Koganezawa et al., 2010, Chen et al., 2008, Windler and Bilder, 2010, Zhang et al., 2010, Nojima et al., 2010, Hebbar and Fernandes, 2010, Poskanzer et al., 2006, Rister et al., 2007, Zhang et al., 2010, Zars, 2010, Xi et al., 2008, Alekseyenko et al., 2010, Yamaguchi et al., 2010, Grygoruk et al., 2010, Ho et al., 2010, Mehnert and Cantera, 2008, Keene et al., 2010, Nahm et al., 2010, Pauls et al., 2010, Saja et al., 2010, Popodi et al., 2010-, Hsouna et al., 2010, Kahsai et al., 2010, Silies and Klämbt, 2010, Kamikouchi et al., 2010, Kim et al., 2010, Dason et al., 2010, Wigby et al., 2011, Yarali and Gerber, 2010, Liu et al., 2010, Roy et al., 2007, Wasbrough et al., 2010, Wasbrough et al., 2010, Yuan et al., 2010, Uytterhoeven et al., 2011, Burke and Waddell, 2011, Ng et al., 2011, Kazama et al., 2011, Vaccari et al., 2008, Han et al., 2011, Akalal et al., 2006, Larkin et al., 2010, Ye et al., 2004, Kopyl et al., 2010, Lee et al., 2011, Houalla et al., 2010, Negreiros et al., 2010, Stümpges and Behr, 2011, Rodal et al., 2008, Kopyl et al., 2010, Yang et al., 2011)
Name Synonym
shibire
(van der Bliek, 1991.5.15, Rikhy et al., 2007, Bokel et al., 2006, Koh et al., 2007, Dickman et al., 2005, Narayanan et al., 2005, Beronja et al., 2005, Ohyama et al., 2007, Zhao et al., 2008, Pocha et al., 2011, Kitamoto, 2002, Trotta et al., 2004, Seto and Bellen, 2006, Zhang et al., 2007, Macleod et al., 2004, Sasaki et al., 2007, Lee and Sun, 2008, Honjo and Furukubo-Tokunaga, 2005, Pai et al., 2006, Kelly and Phillips, 2005, Huang et al., 2006, Lecuit, 2004, Meyer et al., 2006, Chen et al., 2002, Robertson et al., 2000, Ing et al., 2007, Nallamothu et al., 2008, Han et al., 2007, Tsarouhas et al., 2007, Sokac and Wieschaus, 2008, Chang et al., 2008, Callejo et al., 2008, Guha et al., 2003, Hoyer et al., 2008, Heerssen et al., 2008, Behr et al., 2007, Sakai and Kitamoto, 2006, Rister and Heisenberg, 2006, Seugnet et al., 2008, Georgiou et al., 2008, Leibfried et al., 2008, Honjo and Furukubo-Tokunaga, 2009, Nikolaev et al., 2009, Su et al., 2007, Yang et al., 2009, Chiang et al., 2009, Akbergenova and Bykhovskaia, 2009, Zimmermann et al., 2009, Kilman et al., 2009, Pouille et al., 2009, Desai et al., 2009, Hall, 2003, Tanaka et al., 2009, Rajan et al., 2009, Vlisidou et al., 2009, Joseph et al., 2009, Beramendi et al., 2007, Al-Anzi et al., 2009, Gupta et al., 2009, Rogat and Miller, 2002, Hughes and Thomas, 2007, Li et al., 2010, Raghu et al., 2009, Katsuki et al., 2009, Krashes et al., 2009, Hsouna et al., 2007, Fricke et al., 2009, Katsov and Clandinin, 2008, Yao et al., 2009, Huntwork and Littleton, 2007, Vijayakrishnan et al., 2009, Cherry and Perrimon, 2004, Rohrbough and Broadie, 2002, Koenig and Ikeda, 2005, Wu et al., 2005, Koenig and Ikeda, 2007, Potter et al., 2010, Potter et al., 2010, Potter et al., 2010, Chen et al., 2008, Belenkaya et al., 2008, Zhang et al., 2010, Yamaguchi et al., 2010, McPhee et al., 2010, Dason et al., 2010, Roy et al., 2007, Wasbrough et al., 2010, Freeman et al., 2011, Kawasaki et al., 2000, van Swinderen and Greenspan, 2003, Davis, 2004, Keene et al., 2004, Klose et al., 2005, Xu et al., 2008, Gonzalez-Bellido et al., 2009, Koganezawa et al., 2010, Shiraiwa, 2008, Zhou et al., 2008, Hebbar and Fernandes, 2010, Zhang et al., 2010, Nojima et al., 2010, Alekseyenko et al., 2010, Benhra et al., 2010, Burke and Waddell, 2011, Akalal et al., 2006, Ye et al., 2004, Kuromi et al., 2010, Cammarato et al., 2011, Negreiros et al., 2010)
Secondary FlyBase IDs
  • FBgn0030705
  • FBgn0045942
  • FBgn0045943
  • FBgn0045944
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hide Recent research papers ( 61 )
Burke and Waddell, 2011, Curr. Biol. 21(9): 746--750
Remembering nutrient quality of sugar in Drosophila. [FBrf0213625]
Freeman et al., 2011, Mol. Cell. Neurosci. 46(2): 535--547
NFAT regulates pre-synaptic development and activity-dependent plasticity in Drosophila. [FBrf0212894]
Han et al., 2011, Proc. Natl. Acad. Sci. U.S.A. 108(23): 9673--9678
Enhancer-driven membrane markers for analysis of nonautonomous mechanisms reveal neuron-glia interactions in Drosophila. [FBrf0213916]
Iyengar et al., 2011, Genes Brain Behav. 10(8): 883--900
Silencing synaptic communication between random interneurons during Drosophila larval locomotion. [FBrf0216607]
Kawasaki et al., 2011, Proc. Natl. Acad. Sci. U.S.A. 108(25): E222--E229
The DISABLED protein functions in CLATHRIN-mediated synaptic vesicle endocytosis and exoendocytic coupling at the active zone. [FBrf0213990]
Kazama et al., 2011, J. Neurosci. 31(21): 7619--7630
Cell Death Triggers Olfactory Circuit Plasticity via Glial Signaling in Drosophila. [FBrf0213815]
Kohatsu et al., 2011, Neuron 69(3): 498--508
Female Contact Activates Male-Specific Interneurons that Trigger Stereotypic Courtship Behavior in Drosophila. [FBrf0213024]
Lee et al., 2011, Proc. Natl. Acad. Sci. U.S.A. 108(33): 13794--13799
Serotonin-mushroom body circuit modulating the formation of anesthesia-resistant memory in Drosophila. [FBrf0214737]
Mateus et al., 2011, PLoS ONE 6(4): e18729
Endocytic and Recycling Endosomes Modulate Cell Shape Changes and Tissue Behaviour during Morphogenesis in Drosophila. [FBrf0213562]
Ng et al., 2011, Curr. Biol. 21(8): 625--634
Glial cells physiologically modulate clock neurons and circadian behavior in a calcium-dependent manner. [FBrf0213518]
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]
Pinal and Pichaud, 2011, J. Cell Sci. 124(9): 1564--1570
Dynamin- and Rab5-dependent endocytosis is required to prevent Drosophila photoreceptor degeneration. [FBrf0213465]
Pocha et al., 2011, Curr. Biol. 21(13): 1111--1117
Retromer controls epithelial cell polarity by trafficking the apical determinant crumbs. [FBrf0214250]
Sartain et al., 2011, Development 138(8): 1619--1629
The poly(A) polymerase GLD2 is required for spermatogenesis in Drosophila melanogaster. [FBrf0213334]
Sorribes et al., 2011, PLoS Comput. Biol. 7(6): e1002075
The origin of behavioral bursts in decision-making circuitry. [FBrf0214285]
Sousa-Nunes et al., 2011, Nature 471(7339): 508--512
Fat cells reactivate quiescent neuroblasts via TOR and glial insulin relays in Drosophila. [FBrf0214426]
Stümpges and Behr, 2011, FEBS Lett. 585(20): 3316--3321
Time-specific regulation of airway clearance by the Drosophila J-domain transmembrane protein Wurst. [FBrf0216409]
Séjourné et al., 2011, Nat. Neurosci. 14(7): 903--910
Mushroom body efferent neurons responsible for aversive olfactory memory retrieval in Drosophila. [FBrf0214029]
Uytterhoeven et al., 2011, Cell 145(1): 117--132
Loss of skywalker reveals synaptic endosomes as sorting stations for synaptic vesicle proteins. [FBrf0213384]
Wigby et al., 2011, Proc. Biol. Sci. 278(1704): 424--431
Insulin signalling regulates remating in female Drosophila. [FBrf0212666]
Yang et al., 2011, Neuron 72(2): 285--299
Nak regulates localization of clathrin sites in higher-order dendrites to promote local dendrite growth. [FBrf0216477]
Yuva-Aydemir et al., 2011, J. Neurosci. 31(19): 7005--7015
Spinster Controls Dpp Signaling during Glial Migration in the Drosophila Eye. [FBrf0213705]
Ai et al., 2010, Nature 468(7324): 691--695
Acid sensing by the Drosophila olfactory system. [FBrf0212455]
Alekseyenko et al., 2010, PLoS ONE 5(5): e10806
Targeted manipulation of serotonergic neurotransmission affects the escalation of aggression in adult male Drosophila melanogaster. [FBrf0210961]
Benhra et al., 2010, Mol. Biol. Cell 21(12): 2078--2086
Neuralized promotes Basal to apical transcytosis of delta in epithelial cells. [FBrf0211002]
Dason et al., 2010, J. Neurosci. 30(47): 15856--15865
Vesicular sterols are essential for synaptic vesicle cycling. [FBrf0212381]
Grygoruk et al., 2010, J. Biol. Chem. 285(10): 6867--6878
A Tyrosine-based Motif Localizes a Drosophila Vesicular Transporter to Synaptic Vesicles in Vivo. [FBrf0210098]
Hamanaka and Meinertzhagen, 2010, J. Comp. Neurol. 518(7): 1133--1155
Immunocytochemical localization of synaptic proteins to photoreceptor synapses of Drosophila melanogaster. [FBrf0209968]
Hebbar and Fernandes, 2010, Dev. Biol. 340(2): 344--354
Glial remodeling during metamorphosis influences the stabilization of motor neuron branches in Drosophila. [FBrf0210520]
Ho et al., 2010, Development 137(5): 745--754
Echinoid regulates Flamingo endocytosis to control ommatidial rotation in the Drosophila eye. [FBrf0209940]
Houalla et al., 2010, Mol. Brain 3: 19
Rab-mediated vesicular transport is required for neuronal positioning in the developing Drosophila visual system. [FBrf0211130]
Hsouna et al., 2010, Mol. Cell. Biol. 30(15): 3779--3794
Drosophila von hippel-lindau tumor suppressor gene function in epithelial tubule morphogenesis. [FBrf0211250]
Kahsai et al., 2010, J. Exp. Biol. 213(13): 2256--2265
Neuropeptides in the Drosophila central complex in modulation of locomotor behavior. [FBrf0211022]
Kamikouchi et al., 2010, Europ. J. Neurosci. 31(4): 697--703
Mechanical feedback amplification in Drosophila hearing is independent of synaptic transmission. [FBrf0210513]
Keene et al., 2010, Curr. Biol. 20(13): 1209--1215
Clock and cycle Limit Starvation-Induced Sleep Loss in Drosophila. [FBrf0211239]
Kim et al., 2010, Exp. Gerontol. 45(7-8): 611--620
Gene expression profiling implicates OXPHOS complexes in lifespan extension of flies over-expressing a small mitochondrial chaperone, Hsp22. [FBrf0210880]
Koganezawa et al., 2010, Curr. Biol. 20(1): 1--8
The Shaping of Male Courtship Posture by Lateralized Gustatory Inputs to Male-Specific Interneurons. [FBrf0209959]
Kopyl et al., 2010, Russ. J. Genet. 46(3): 276--282
Drosophila melanogaster gene Merlin interacts with the clathrin adaptor protein gene lap. [FBrf0215199]
Kopyl et al., 2010, Genetika, Moscow 46(3): 314--320
[Drosophila melanogaster gene Merlin interacts with the clathrin adaptor protein gene lap] [FBrf0210615]
Kuromi et al., 2010, Europ. J. Neurosci. 32(3): 335--346
Two types of Ca channel linked to two endocytic pathways coordinately maintain synaptic transmission at the Drosophila synapse. [FBrf0211498]
Larkin et al., 2010, Learn. Mem. 17(12): 645--653
Central synaptic mechanisms underlie short-term olfactory habituation in Drosophila larvae. [FBrf0212326]
Li et al., 2010, EMBO J. 29(5): 992--1006
Bicaudal-D binds clathrin heavy chain to promote its transport and augments synaptic vesicle recycling. [FBrf0210180]
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]
McPhee et al., 2010, Nature 465(7301): 1093--1096
Activation of autophagy during cell death requires the engulfment receptor Draper. [FBrf0211145]
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]
Negreiros et al., 2010, genesis 48(1): 31--43
alphaPS1betaPS integrin receptors regulate the differential distribution of Sog fragments in polarized epithelia. [FBrf0209674]
Nojima et al., 2010, Curr. Biol. 20(9): 836--840
Neuronal synaptic outputs determine the sexual fate of postsynaptic targets. [FBrf0210762]
Pauls et al., 2010, J. Neurosci. 30(32): 10655--10666
Drosophila Larvae Establish Appetitive Olfactory Memories via Mushroom Body Neurons of Embryonic Origin. [FBrf0211533]
Potter et al., 2010, Cell 141(3): 536--548
The Q system: a repressible binary system for transgene expression, lineage tracing, and mosaic analysis. [FBrf0210697]
Quinones et al., 2010, J. Cell Biol. 189(2): 353--367
I-BAR protein antagonism of endocytosis mediates directional sensing during guided cell migration. [FBrf0210570]
Saja et al., 2010, Neurobiol. Disease 40(1): 135--145
Identifying cellular pathways modulated by Drosophila palmitoyl-protein thioesterase 1 function. [FBrf0211567]
Sidyelyeva et al., 2010, Cell. Molec. Life Sci. 67(17): 2991--3004
Individual carboxypeptidase D domains have both redundant and unique functions in Drosophila development and behavior. [FBrf0211540]
Silies and Klämbt, 2010, Nat. Neurosci. 13(11): 1357--1364
APC/C(Fzr/Cdh1)-dependent regulation of cell adhesion controls glial migration in the Drosophila PNS. [FBrf0212144]
Wasbrough et al., 2010, J. Proteomics 73(11): 2171--2185
The Drosophila melanogaster sperm proteome-II (DmSP-II). [FBrf0211978]
Windler and Bilder, 2010, Curr. Biol. 20(6): 538--543
Endocytic internalization routes required for delta/notch signaling. [FBrf0210409]
Yamaguchi et al., 2010, Proc. Natl. Acad. Sci. U.S.A. 107(12): 5634--5639
Contribution of photoreceptor subtypes to spectral wavelength preference in Drosophila. [FBrf0210366]
Yarali and Gerber, 2010, Front. Behav. Neurosci. 4: 189
A Neurogenetic Dissociation between Punishment-, Reward-, and Relief-Learning in Drosophila. [FBrf0212711]
Yu et al., 2010, J. Neurosci. 30(36): 12151--12156
Plexin a-semaphorin-1a reverse signaling regulates photoreceptor axon guidance in Drosophila. [FBrf0211784]
Yuan et al., 2010, J. Cell Sci. 123(6): 939--946
Analysis of integrin turnover in fly myotendinous junctions. [FBrf0213429]
Zhang et al., 2010, Curr. Biol. 20(7): 591--599
DN1(p) circadian neurons coordinate acute light and PDF inputs to produce robust daily behavior in Drosophila. [FBrf0210593]
hide Recent reviews ( 1 )
Zars, 2010, Learn. Mem. 17(5): 246--251
Short-term memories in Drosophila are governed by general and specific genetic systems. [FBrf0210637]