A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\Nl1N-ts2

General Information
SymbolDmel\Nl1N-ts2SpeciesD. melanogaster
NameFlyBase IDFBal0012888
Feature typealleleAssociated geneDmel\N
Also Known AsNts2
Allele classheat sensitive hypomorphic allele - genetic evidence
Mutagenethyl methanesulfonate
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Description
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FB2013_03
FB2013_02
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Cytology
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Wound healing does not appear to be affected compared to controls in N[l1N-ts2]/+ wing discs which have been fragmented (a 90[o] sector has been dissected out of the posterior compartment, leaving a 3/4 anterior fragment) and then implanted into wild-type females (analysed at 24 and 48 hours after implantation). However, the N[l1N-ts2]/+ regenerating discs show significantly impaired proliferation compared to controls.
Stage 10 N[l1N-ts2] homozygous females, that have been shifted to a non-permissive temperature for less than 6 hours exhibit migration defects, despite these egg chambers already developing to stage 9, and follicle cell differentiation occurring, prior to the temperature shift (whereas wild-type controls exhibited no migration defects).
Adult flies show normal reactivity to electric shock and normal olfactory acuity (to methylcyclohexanol and octanol) after incubation at the restrictive temperature (30oC) for 2 days. Adult flies incubated for 2 days at the restrictive temperature show normal learning scores in a Pavlovian learning and memory assay. However, these flies show a significant reduction in one-day memory after spaced training compared to flies maintained at the permissive temperature.
When Nl1N-ts2 mutants are shifted to restrictive temperature between 104 and 128 h after egg laying (AEL) (8-32h after puparium formation (APF)), the L3 vein is broader, indicative of abnormal vein resolution. The campaniform sensillae (CS) are centered over the broader vein. When a transient temperature shift is applied at 60-80 h AEL, the L3 vein retains a wild-type width but its position is shifted anteriorly relative to the CS.
Shifting Nl1N-ts2 mutant larvae to the nonpermissive temperature in mid-late-L1 results in eye-antennal discs that are reduced in size.
Mutant larvae shifted to the non-permissive temperature (29oC) at the beginning of the L2 stage have abnormal wing discs. Mutant larvae shifted to the non-permissive temperature (29oC) at the beginning of the L3 stage have wing discs with a smaller wing pouch than normal. Adults derived from these larvae have notches at the distal tip of the wing.
Weak embryonic neurogenic phenotype at 29oC.
Lethal in combination with Df(1)N-8 at both 18oC and 29oC. 8% of homozygotes survive at 29oC, 97% survive at 18oC. Wings are normal in heterozygotes. Homozygotes are morphologically normal at 18oC. At 29oC, late pupae are head-eyeless, have a rough eye, stubby legs and irregular chaetae. Lethal in combination with Nl1N-ts1 at 29oC. 40% of Nl1N-ts2/NAx-tsl flies survive at 29oC and have an abruptex phenotype.
Similar to Nl1N-ts1 except for occasional survival of homozygotes to the pupal stage at 29oC and weaker expression of recessive visible defects in heterozygotes at this temperature.
 
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Fails to complement
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Failure to complement is at 29oC, complementation is at 18oC.
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Bloomington
Kyoto
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Discoverer
Shellenbarger.
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Reported As
Symbol Synonym
Nl1N-ts2
 
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hide References ( 13 )
Research paper
Blanco et al., 2010, BMC Dev. Biol. 10: 94
Gene expression following induction of regeneration in Drosophila wing imaginal discs. Expression profile of regenerating wing discs. [FBrf0211812]
Scherfer et al., 2008, Dev. Biol. 323(2): 189--196
Drosophila Serpin-28D regulates hemolymph phenoloxidase activity and adult pigmentation. [FBrf0207215]
Krzemień et al., 2007, Nature 446(7133): 325--328
Control of blood cell homeostasis in Drosophila larvae by the posterior signalling centre. [FBrf0194113]
Wang et al., 2007, Dev. Biol. 301(2): 532--540
Spatially localized Kuzbanian required for specific activation of Notch during border cell migration. [FBrf0191839]
Herranz et al., 2006, EMBO Rep. 7(3): 297--302
Self-refinement of Notch activity through the transmembrane protein Crumbs: modulation of gamma-Secretase activity. [FBrf0190373]
Ge et al., 2004, Proc. Natl. Acad. Sci. U.S.A. 101(27): 10172--10176
Notch signaling in Drosophila long-term memory formation. [FBrf0179219]
Lee and Adler, 2004, Mech. Dev. 121(1): 37--49
The grainy head transcription factor is essential for the function of the frizzled pathway in the Drosophila wing. [FBrf0167844]
Crozatier et al., 2003, Mech. Dev. 120(5): 529--535
Vein-positioning in the Drosophila wing in response to Hh; new roles of Notch signaling. [FBrf0160464]
Kenyon et al., 2003, Dev. Cell 5(3): 403--414
Coordinating proliferation and tissue specification to promote regional identity in the Drosophila head. [FBrf0162063]
Glise et al., 2002, Dev. Biol. 248(1): 93--106
Notch and wingless modulate the response of cells to hedgehog signalling in the Drosophila wing. [FBrf0151253]
Lehmann et al., 1983, Rouxs Arch. Dev. Biol. 192(2): 62--74
On the phenotype and development of mutants of early neurogenesis in Drosophila melanogaster. [FBrf0040185]
Shellenbarger and Mohler, 1975, Genetics 81: 143--162
Temperature-sensitive mutations of the Notch locus in Drosophila melanogaster. [FBrf0027480]
Shellenbarger, 1972, D. I. S. 48: 55
Evidence that EMS induces point mutations at high frequency. [FBrf0023652]