Insertion in a protein coding exon common to both BEAF-32 A and B isoforms.
BEAF-32NP6377/Df(2R)BSC429 animals and homozygous BEAF-32NP6377 retinal clones (covering the entire retina) have an increased proportion of pale R8 photoreceptors and a reciprocally decreased proportion of yellow R8 photoreceptors, compared to controls.
FlyBase curator comment: FBrf0219796 reports that the chromosome carrying the P{GawB}BEAF-32NP6377 insertion is homozygous lethal and causes neoplastic growth phenotypes. A subsequent report (FBrf0224638) provides evidence that these phenotypes are not due to an effect on BEAF-32, but are instead due to second-site mutations on the chromosome carrying the P{GawB}BEAF-32NP6377 insertion.
The homozygous larval lethality of the NP6377 chromosome is not due to the P{GawB}BEAF-32NP6377 insertion in BEAF-32, but is instead due to second site mutation(s): the lethality of the NP6377 chromosome is not rescued by BEAF-32+t5 or BEAF-32EGFP, and BEAF-32AB-KO (a null allele of BEAF-32) complements the lethality of the NP6377 chromosome.
Flies carrying BEAF-32AB-KO over the NP6377 chromosome were found to be viable and could be maintained as a healthy stock over 25 generations. This was unexpected as BEAF-32AB-KO/BEAF-32AB-KO homozygous females are almost sterile (see FBrf0200670). This suggests that in addition to the second site lethality, the NP6377 chromosome also carries another second site mutation: a dominant mutation that suppresses the female fertility defect caused by a lack of BEAF-32 protein. FlyBase curator comment: this second site dominant suppressor of BEAF-32 mutant female sterility has subsequently been named Tofu1 (see FBrf0255826).
The two second site mutations on the NP6377 chromosome (lethality and dominant suppressor of BEAF-32 mutant female sterility) are separable and therefore do not appear to be caused by the same mutation.
Separable from: Tofu1.