A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Dmel\P{PZ}Rca103300 Insertion

General Information
Symbol Dmel\P{PZ}Rca103300 Species D. melanogaster
Name FlyBase ID FBti0005236
Feature type transposable_element_insertion_site
Description
Inserted element P{PZ} Expression data lacZ reporter
Affected gene(s) Ecol\lacZ, Rca1 Viability / fertility
Causes allele(s) Ecol\lacZRca1-03300, Rca103300 Stock availability 2 publicly available
LINE ID l(2)03300
Genomic Location
Chromosomal location 2L ( 27C1 ) Sequence location 2L:6,852,365..6,852,365 [+]
Map ( GBrowse ) detailed view FBti0053821 FBti0041621 FBti0005236 FBti0006601
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Description
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FB2012_01
FB2011_10
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hide Detailed Mapping Data
Chromosome (arm)
Sequence Location
2L:6,852,365..6,852,365 [+]
Orientation
Cytological location
(computed by FlyBase)
27C1 ( inferred by FlyBase from sequence location )
Cytological location
(reported)
27B4-27C1 (in situ hybridization reported)
Comments concerning
location
hide Sequence Data
Flanking sequence
hide Inserted Element
Construct P{PZ}
Location-dependent
role
lacZ enhancer trap
Size 14.545Kb
Associated alleles
Molecular map
hide Affected Gene(s)
Insertion may
affect gene
hide Alleles and Phenotypes
Causes alleles
Lethality
References
lethal | recessive
semi-lethal
 
Sterility
References
hide Phenotype Manifest In
abdominal segment 2 & cardioblast
abdominal segment 3 & cardioblast
abdominal segment 4 & cardioblast
abdominal segment 5 & cardioblast
abdominal segment 6 & cardioblast
abdominal segment 7 & cardioblast
aCC neuron | precursor
EL neuron
embryonic pericardial cell
ganglion mother cell
ganglion mother cell GMC1-1a
ganglion mother cell GMC4-2a
pCC neuron
pCC neuron | precursor
RP2sib neuron
U neuron
hide Detailed Description
Statement
Reference
86% of mutant embryos lack eve expressing pericardial cells (EPC), the rest show one EPC per hemisegment (instead of the two seen in wild-type). DA1 muscles form as in wild-type. A halving is also seen in the number of myocardial cells seen in segments A2 to A7, though the number seen in segments T3 to A1 remain normal.
In mutant embryos, the ganglion mother cells, GMC1-1a and GMC4-2a fail to divide into their normal progeny. The non-dividing GMC1-1a and GMC4-2a cells are larger than normal and sit where its offspring should normally be. A loss of approximately 10% of EL neurons is also seen.
In mutant embryos the division of neurons are affected in a lineage specific manner. The ganglion mother cell (GMC) of the RP2/sib lineage fails to divide, and assumes the identity of the RP2 neuron. The GMC of the aCC/pCC lineage is similarly affected; it fails to divide and assumes the identity of the aCC. These phenotypes are fully penetrant. Timing and axonal projections from these neurons continue as if they were wildtype. Other lineages are also affected in mutant embryos. The CQ lineage fails to divide in about 50% of hemisegments and the U lineage fails to divide in 65% of hemisegments. The effect on the EL line is minimal.
Dominantly enhances the rough eye phenotype of CycEJP homozygotes. One copy of Rca103300 has no effect on the reduction in the number of cells entering S phase posterior to the morphogenetic furrow seen in CycEJP homozygotes.
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Reporter Expression
distribution deduced from reporter
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Information
Statement
Reference
In the adult brain, expressed in the central brain and the optic lobe.
In wandering third instar larva, no detectable β-gal staining.
Marker for
Reflects
expression of
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FlyView (LinkOut)
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Line ID
Origin as a multiple insertion line
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hide Related Aberration or Balancer
Aberration
Balancer
hide Stocks ( 2 )
Bloomington
Kyoto
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hide Synonyms & Secondary IDs
Reported As
Symbol Synonym
P{PZ}l(2)0330003300
P{PZ}Rca103300
P{ry+t7.2=PZ}l(2)0330003300
Secondary FlyBase IDs
  • FBti0000315
hide References ( 14 )
Research paper
Bellen et al., 2004, Genetics 167(2): 761--781
The BDGP gene disruption project: single transposon insertions associated with 40% of Drosophila genes. [FBrf0179132]
Han and Bodmer, 2003, Development 130(13): 3039--3051
Myogenic cells fates are antagonized by Notch only in asymmetric lineages of the Drosophila heart, with or without cell division. [FBrf0160590]
Lear et al., 1999, Mech. Dev. 88(2): 207--219
Neural cell fate in rca1 and cycA mutants: the roles of intrinsic and extrinsic factors in asymmetric division in the Drosophila central nervous system. [FBrf0111940]
Spradling et al., 1999, Genetics 153(1): 135--177
The Berkeley Drosophila genome project gene disruption project. Single P-element insertions mutating 25% of vital Drosophila genes. [FBrf0111489]
Wai et al., 1999, Development 126(12): 2759--2770
Cell division genes promote asymmetric interaction between numb and Notch in the Drosophila CNS. [FBrf0109136]
Russell et al., 1998, Genome 41(1): 7--13
Lethal P-lacZ insertion lines expressed during pattern respecification in the imaginal discs of Drosophila. [FBrf0102000]
Secombe et al., 1998, Genetics 149(4): 1867--1882
Analysis of a Drosophila cyclin E hypomorphic mutation suggests a novel role for cyclin E in cell proliferation control during eye imaginal disc development. [FBrf0103367]
Dong et al., 1997, Genes Dev. 11(1): 94--105
Control of G1 in the developing Drosophila eye: rca1 regulates Cyclin A. [FBrf0091048]
Mlodzik and Hiromi, 1992, Conn, 1992: 397--414
Enhancer trap method in Drosophila: its application to neurobiology. [FBrf0066714]
Personal communication to FlyBase
Vosshall, 1998.8.10, Patterns of lacZ expression.
Patterns of lacZ expression. [FBrf0103142]
Meister and Braun, 1995.10, lacZ expression patterns for P{} insertions at Bloomington.
lacZ expression patterns for P{} insertions at Bloomington. [FBrf0083714]
FlyBase analysis
FlyBase, 1992-, FlyBase curation
FlyBase curation. [FBrf0105495]
Computer file
Gene Disruption Project members, 2001-, [title not yet available]
[title not yet available] [FBrf0132177]
BDGP Project Members, 1994-1999, Berkeley Drosophila Genome Project.
Berkeley Drosophila Genome Project. [FBrf0067338]