P{PTT-GB}RpL10AbCB02653 is inserted -34bp upstream of the RpL10Ab transcriptional start site.
Insertion upstream of the transcription start site (insertion is 1-500bp upstream of the start site), in the appropriate predicted reading frame to fuse the GFP exon in the inserted construct to the endogenous protein.
RpL10AbCB02653 germline clones fail to progress into mid-oogenesis. Approximately 36% of dying egg chambers exhibit a loss of follicle cells around the egg chamber, while the nurse cells appear normal. Nuclei of RpL10AbCB02653 germline follicle cells display abnormal morphology and are much larger than heterozygous nuclei. Moreover, the nucleoli of these clones are larger and more prominent compared to controls. RpL10AbCB02653 germline clones are larger and reduced in number compared to controls, suggesting a defect in proliferation or survival. Only 19% of RpL10AbCB02653 stage 10 egg chambers exhibit follicle cell clones.
RpL10AbCB02653 has lethal - all die before end of larval stage phenotype, suppressible | partially by Fmer\RpL10AUAS.cWa/Scer\GAL4Act5C.PI
RpL10AbCB02653 has lethal - all die before end of larval stage phenotype, suppressible | partially by Fmer\RpL10AUAS.cWa/Scer\GAL4arm.PS
Ubiquitous expression of Zzzz\RpL10AScer\UAS.cWa under the control of Scer\GAL4Act5C.PI, leads to 37% viability of RpL10AbCB02653 flies whereas expression under the control of Scer\GAL4arm.PS leads to 39% viability in RpL10AbCB02653 mutants. In addition, these rescued flies are fertile, indicating that Zzzz\RpL10AScer\UAS.cWa has functional conservation with RpL10Ab.
Protein trap line.