P{SUPor-P}RpL10AbKG09231 is inserted -28bp upstream of the RpL10Ab transcriptional start site.
RpL10AbKG09231 germline clones fail to progress into mid-oogenesis. Approximately 50% of dying egg chambers exhibit a loss of follicle cells around the egg chamber, while the nurse cells appear normal. Nuclei of RpL10AbKG09231 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. RpL10AbKG09231 germline clones are larger and reduced in number compared to controls, suggesting a defect in proliferation or survival. Only 23% of RpL10AbKG09231 stage 10 egg chambers exhibit follicle cell clones.
RpL10AbKG09231 has lethal - all die before end of larval stage phenotype, suppressible | partially by Fmer\RpL10AUAS.cWa/Scer\GAL4Act5C.PI
RpL10AbKG09231 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 16% viability of RpL10AbKG09231 flies whereas expression under the control of Scer\GAL4arm.PS leads to 38% viability in RpL10AbKG09231 mutants. In addition, these rescued flies are fertile, indicating that Zzzz\RpL10AScer\UAS.cWa has functional conservation with RpL10Ab.