P{lacW} insertion in exon 1.
The P{lacW}Nrkk14301 insertion maps within both TppII and CG34439 (overlapping genes on opposite strands) by BLAST analysis of the flanking sequence of the insertion. In addition, in FBrf0139680, the P{lacW}Nrkk14301 insertion is stated to map "within the 5' end of an alternative-splice form of Nrk" (Nrk is located downstream to CG34439, and overlaps it on the same strand).
FlyBase curator comment: Interactions with Dg[086] and/or Dg[323] were detected in a Dg[086]/+ or Dg[323]/+ background which exhibits no obvious changes in muscle morphology. Nonetheless, these interactions have been captured as 'modifier' ('exacerbates') annotations here to best capture the experimental finding and the authors' intention.
Nrk[+]/Nrkk14301 is a suppressor of visible phenotype of DysRNAi.NH2.UAS, Scer\GAL4Act.PU
Nrk[+]/Nrkk14301 is a suppressor of visible phenotype of DysRNAi.C.UAS, Scer\GAL4Tub.PU
Df(3R)Exel6184/+, Nrkk14301 has abnormal neuroanatomy | third instar larval stage phenotype
Nrk[+]/Nrkk14301 is a non-enhancer of indirect flight muscle cell phenotype of DysRNAi.NH2.UAS, Scer\GAL4Act.PU
Nrk[+]/Nrkk14301 is a non-enhancer of indirect flight muscle cell phenotype of DgRNAi.UAS, Scer\GAL4Act.PU
Nrk[+]/Nrkk14301 is a suppressor of posterior crossvein phenotype of DysRNAi.NH2.UAS, Scer\GAL4Act.PU
Nrk[+]/Nrkk14301 is a suppressor of posterior crossvein phenotype of DysRNAi.C.UAS, Scer\GAL4Tub.PU
Df(3R)Exel6184/+, Nrkk14301 has indirect flight muscle cell phenotype
Dg[+]/DgO86, Nrkk14301 has indirect flight muscle cell phenotype
Dg[+]/Dg323, Nrkk14301 has indirect flight muscle cell phenotype
Df(3R)Exel6184/+, Nrkk14301 has lamina plexus | third instar larval stage phenotype
DysRNAi.C.UAS, Nrk[+]/Nrkk14301 has wing vein | ectopic phenotype
Nrk Dys double heterozygous flies (Nrkk14301/Df(3R)Exel6184) exhibit indirect flight muscle degeneration.
Nrkk14301 DgO86 double heterozygous flies exhibit indirect flight muscle degeneration.
One copy of Nrkk14301 does not enhance the indirect flight muscle degeneration seen when DysdsRNA.NH2.Scer\UAS is expressed under the control of Scer\GAL4Act.PU.
One copy of Nrkk14301 does not enhance the indirect flight muscle degeneration seen when DgdsRNA.Scer\UAS is expressed under the control of Scer\GAL4tub.PU.
Nrkk14301 Dg323 double heterozygous flies exhibit indirect flight muscle degeneration.
Combination of Df(3R)Exel6184 in heterozygous state with a single copy of Nrkk14301 results in a significantly increased frequency of lamina plexus defects in the third instar larval brain, whereas the rhabdomere length in the adult eye remains unaffected in the double heterozygotes.
Combination of DgO86 in heterozygous state with a single copy of Nrkk14301 does not significantly affect either the frequency of lamina plexus defects in the third instar larvae or the rhabdomere length in the adults.
One copy of Nrkk14301 weakly suppresses the detached posterior crossvein phenotype seen when DysdsRNA.NH2.Scer\UAS is expressed under the control of Scer\GAL4Act.PU.
One copy of Nrkk14301 moderately suppresses the detached posterior crossvein phenotype seen when DysdsRNA.C.Scer\UAS is expressed under the control of Scer\GAL4tub.PU but produces extra wing vein material.
The P{lacW}Nrkk14301 insertion (which is inserted into 2 overlapping genes; intron 1 of TppII and exon 1 of Nrk) is a moderate dominant enhancer of the Ras85Dix12a eggshell phenotype; 31-40% of dorsal appendages are wild type.
I. Kiss.
This allele was listed in the BDGP database as a lethal or sterile line during the period 1994-1999, but was discarded from the gene disruption project prior to the summary publication (FBrf0111489). Reasons for excluding lines from the collection described in FBrf0111489 include presence of more than one P insertion on the mutant chromosome, separation of lethality (or sterility) from the location of the insertion, and loss of lethality (or sterility) from the stock. Further information is available from http://www.fruitfly.org/bfd/ and from Dr. Spradling (spradling@mail1.ciwemb.edu).
Complements: Aats-val03531. Complements: Aats-valk14312. Complements: Aats-valk14804. Complements: Aats-valrI255. Complements: Aats-valrQ802.