The open reading frame of the endogenous RpS5b locus has been deleted and replaced by a cassette that encodes 1. a Disc\RFPDsRed(T1).3xP3.cHa marker flanked by loxP sites (allowing subsequent removal of this marker from a targeted locus), and 2. a single attP site.
In RpS5bCRISPR homozygous females, egg chambers do not complete stage 8; stage 7/8 egg chambers exhibit an abnormal nuclear structure and multiple layered follicle cells within the posterior region; stage 8 oocytes do not accumulate yolk granules; stage 7 RpS5bCRISPR egg chambers display increased frequency of follicle cells undergoing mitosis, which is only observed in the posterior region of the egg chamber; stage 8 oocytes show a reduced and unpolarized microtubule cytoskeleton.
RpS5bCRISPR has decreased fecundity | female phenotype, suppressible by RpS5aUAS.cJa/Scer\GAL4VP16.mat.αTub67C
RpS5bCRISPR has female sterile phenotype, suppressible by RpS5aUAS.cJa/Scer\GAL4VP16.mat.αTub67C
RpS5bCRISPR has abnormal cell number | oogenesis phenotype, suppressible | partially by Scer\GAL4vas.PU/RpS5aGL01502
RpS5bCRISPR has abnormal cell number | oogenesis phenotype, suppressible | partially by Scer\GAL4GMR45D11/Nintra.GS.UAS
RpS5bCRISPR has nucleolus | oogenesis stage S7 phenotype, suppressible | partially by RpS5aUAS.cJa/Scer\GAL4VP16.mat.αTub67C
RpS5bCRISPR has posterior terminal follicle cell | oogenesis stage S7 phenotype, suppressible | partially by RpS5aUAS.cJa/Scer\GAL4VP16.mat.αTub67C
RpS5bCRISPR has posterior terminal follicle cell | oogenesis stage S8 phenotype, suppressible | partially by RpS5aUAS.cJa/Scer\GAL4VP16.mat.αTub67C
RpS5bCRISPR has posterior terminal follicle cell | oogenesis stage S7 phenotype, suppressible | partially by Scer\GAL4GMR45D11/Nintra.GS.UAS
RpS5bCRISPR has posterior terminal follicle cell | oogenesis stage S8 phenotype, suppressible | partially by Scer\GAL4GMR45D11/Nintra.GS.UAS
RpS5bCRISPR is partially rescued by RpS5bUAS.cJa/Scer\GAL4VP16.mat.αTub67C