Imprecise excision of P{lacW}neros1921 generates a small deletion that removes 189bp of the nero open-reading frame.
nero1 mutants die as second instar (L2) larvae, whether they are homozygous or in heteroallelic combinations ((with Df(3R)04661).
nero1 mutants cause both mild bristle loss and a severe reduction in bristle size. nero1 mutant socket cells are specified but fail to reach their mature size. Cells adjacent to nero1 exhibit mutant bristles that are smaller in size as indicated by trichome size and spacing. Ectodermal cells that lack nero in the developing thoraxes 47APF are significantly smaller than adjacent wild-type cells.
Rhabdomere size in nero1 mutant eye clones are also reduced when compared with adjacent wild-type cells, suggesting a defect in photoreceptor size.
nero1 mutant clones generated using the Scer\FLP1ey.PN technique are generally irrecoverable. However, nero1 mutant clones are easily obtained using Scer\FLP1ey.PN when cell competition is ameliorated through the use of an FRT chromosome bearing a cell lethal mutation that effectively removes the mitotic wild-type, sister twin cells. Indeed, nero1 mutant clones generated using this technique completely overtake the eye, leading to eyes and heads that are much smaller than wild-type heads.
nero1 mutant clones generated in the wing imaginal disc are smaller and contain fewer cells than their associated wild-type twin spots. The differences in cell number between nero1 clones and their wild-type twin spots are less obvious in small clones and clearly increase as clones get larger. This is likely caused by differences in nero protein perdurance in small clones. nero mutant cells are most likely eliminated because of an inability to compete with wild-type cells.
nero1 mutant larval fat bodies prominently display enlarged, acidified structures, even when the animals are fed an amino acid source, suggesting that nero1 mutant larvae undergo a constitutive starvation response in the presence of an amino acid source.
nero1 mutant clones show a decreased level of BrdU incorporation, indicating a delay in cell cycle progression.
nero1 is an enhancer of decreased cell size phenotype of eEF501296
nero1 is a suppressor of abnormal developmental rate phenotype of Tsc1Q87X
nero1 has microchaeta | somatic clone phenotype, suppressible by Hsap\DOHHUAS.cPa/Scer\GAL4Tub.PU
nero1 has microchaeta | somatic clone phenotype, non-suppressible by eEF5UAS.cPa/Scer\GAL4Tub.PU
nero1 has microchaeta | somatic clone phenotype, non-suppressible by Scer\GAL4Tub.PU/Hsap\DOHHH56A.UAS
nero1 has microchaeta | somatic clone phenotype, non-suppressible by Hsap\DOHHH89A.UAS/Scer\GAL4Tub.PU
nero1 has microchaeta | somatic clone phenotype, non-suppressible by Scer\GAL4Tub.PU/Hsap\DOHHH208A.UAS
nero1 has microchaeta | somatic clone phenotype, non-suppressible by Hsap\DOHHH240A.UAS/Scer\GAL4Tub.PU
eIF-5A01296; nero1 double mutant larvae display a slightly more severe larval growth defect than eIF-5A01296 mutants alone.
Unlike either nero1 or Tsc1Q87X mutant clones, Tsc1Q87X nero1 double mutant clones cannot be recovered. Tsc1Q87Xfully suppresses the autophagic defect seen in nero1 mutant animals. However, this epistatic relationship is reveresed in other contexts such as larval growth and developmental timing. Tsc1Q87X mutant larvae appear to undergo precocious development. However, this precocious development is suppressed in Tsc1Q87X nero1 double mutant larvae.
Overexpression of eIF-5AScer\UAS.cPa (under the control of Scer\GAL4tub) is not sufficient to rescue bristle size defects associated with nero1 mutant clones.
Overexpression of Hsap\DOHHScer\UAS.cPa fully complements defects in bristle size associated with nero1 mutant clones on the thorax and does not cause any other obvious phenotype.
Overexpression of Hsap\DOHHH56A.Scer\UAS fails to suppress the defects in bristle size associated with nero1 mutant clones on the thorax and does not cause any other obvious phenotype.
Overexpression of Hsap\DOHHH89A.Scer\UAS fails to suppress the defects in bristle size associated with nero1 mutant clones on the thorax and does not cause any other obvious phenotype.
Overexpression of Hsap\DOHHH208A.Scer\UAS fails to suppress the defects in bristle size associated with nero1 mutant clones on the thorax and does not cause any other obvious phenotype.
Overexpression of Hsap\DOHHH240A.Scer\UAS fails to suppress the defects in bristle size associated with nero1 mutant clones on the thorax and does not cause any other obvious phenotype.
nero1 is rescued by neroUAS.cPa/Scer\GAL4Act5C.PP
Overexpression of eIF-5AScer\UAS.cPa (under the control of Scer\GAL4tub) is not sufficient to rescue bristle size defects associated with nero1 mutant clones.