A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\Tap42Δ305b

General Information
SymbolDmel\Tap42Δ305bSpeciesD. melanogaster
NameFlyBase IDFBal0181305
Feature typealleleAssociated geneDmel\Tap42
Allele class
MutagenP-element activity
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Description
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FB2013_03
FB2013_02
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Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Imprecise excision of the P{lacW}Nnp-1k07826 element, which removes the element and 1.6kb of sequences downstream. This deletion extends through the transcription and translation start sites of Tap42 and removes the first 8 codons of the Tap42 coding region.
Caused by aberration
Cytology
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Statement
Reference
Tap42Δ305b animals (Df(2L)Tap42Δ305b homozygotes in which lack of Nnp-1 and CG6523 function has been rescued using the P{Nnp-1t5.1} transgene) progress to the early third larval instar with a slight developmental delay and die shortly thereafter, between 96 and 120 hours after egg laying. Tap42Δ305b larvae (Df(2L)Tap42Δ305b homozygotes in which lack of Nnp-1 and CG6523 function has been rescued using the P{Nnp-1t5.1} transgene) have smaller and poorly organised mitotic spindles in the central nervous system compared to controls and most mitotic chromosomes are in a highly condensed metaphase configuration (no mitotic cells in anaphase or telophase have been observed). Third larval instar mutant brains contain pyknotic nuclei. Clones of cells lacking Tap42 function (homozygous for Df(2L)Tap42Δ305b, and with lack of Nnp-1 and CG6523 function rescued by the P{Nnp-1t5.1} transgene) show no change in cell size compared to control cells, and the cell cycle phasing of the mutant cells is indistinguishable from that of wild-type controls. Although clones of cells lacking Tap42 function (homozygous for Df(2L)Tap42Δ305b, and with lack of Nnp-1 and CG6523 function rescued by the P{Nnp-1t5.1} transgene) can be readily identified in wing discs 48 hours after induction, by 72 hours after induction they are no longer present. Mutant clones induced using the Minute technique can persist to 72 hours, but show signs of massive cell death, with highly condensed pyknotic nuclei, and these clones are eliminated at later timepoints. Mutant clones in the eye imaginal discs can survive beyond the 72 hour period in the mitotically quiescent region posterior to the morphogenetic furrow, but not in the mitotically active anterior region.
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Statement
Reference
Tap42Δ305b is a non-suppressor of increased cell size phenotype of Ptendj189
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Statement
Reference
Clones of Ptendj189 Tap42Δ305b double mutant cells (homozygous for Ptendj189 and Df(2L)Tap42Δ305b and with the lack of Nnp-1 and CG6523 function caused by Df(2L)Tap42Δ305b rescued using the P{Nnp-1t5.1} transgene) show the characteristic increase in cell size and S/G2 content of Ptendj189 single mutants.
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hide Synonyms & Secondary IDs ( 1 )
Reported As
Symbol Synonym
Tap42Δ305b
 
Name Synonym
Secondary FlyBase IDs
hide References ( 1 )
Research paper
Cygnar et al., 2005, Genetics 170(2): 733--740
The phosphatase subunit tap42 functions independently of target of rapamycin to regulate cell division and survival in Drosophila. [FBrf0188576]