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. Author manuscript; available in PMC: 2021 Apr 20.
Published in final edited form as: J Genet Genomics. 2020 Mar 19;47(4):187–199. doi: 10.1016/j.jgg.2020.02.008

Fig. 6.

Fig. 6.

dP75 and Jil-1 function together to ensure oogenesis. A: Expression of genes measured by RNA-Seq. Gene expression is calculated as FPKM, and both the x-axis and y-axis are in log2 scale. B: dP75 and Jil-1 protect common targets for transcription. C: DAPI staining shows similar defects of germ cells by either depleting of dP75 or Jil-1 in germ cells. Upper panel: arrow heads point the nurse cells failed to pass the five-blob configuration. Percentage of each panel: 100% in GLD of mCherry (normal morphology); 57% in GLD of Jil-1 (abnormal morphology); 71% in GLD of dP75 (abnormal morphology). Stage 7 to stage 9 egg chambers were observed for quantification. Lower panel: oocyte DNA failed to compact into karyosome (pointed by arrow head). Percentage of each panel: 98% in GLD of mCherry (normal morphology), 34% in GLD of Jil-1 (abnormal morphology), 27% in GLD of dP75 (abnormal morphology). Stage 7 to stage 8 egg chambers were observed for quantification.