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. 2018 Feb 13;7:e32421. doi: 10.7554/eLife.32421

Figure 4. GSC nucleolar morphology and rDNA copy number decrease is heritable.

Figure 4.

(A) Scheme for aging of flies and collection of F1 progeny from old parents. (B) rDNA quantification from testes by qPCR in P0 at 0 and 40 days, and F1 at 0 days. Mean ±SD (p-value *≤0.05, t-test). (C) GSC nucleolar morphology in young P0, old P0 and young F1, as a percentage of total GSCs scored (n, number of GSCs scored). p-values from chi-squared test are shown. (D) Nucleolar dominance assessed by SNP in situ in GSCs from young P0, old P0 and young F1 (n, number of GSCs scored). Mean ±SD. p-value of t-test is shown. Note that ‘X-only’ rRNA transcription was never observed. (E) Y:X signal intensity ratio for the 18S rDNA and 240-IGS in mitotic germ cells comparing day 0 P0 Y and day 0 F1 Y (from day 40 father). Day 0 vs. day 40 fathers (P0) were mated to day 0 old females to yield P0 Y/X vs. F1 Y/X ratio, where X comes from the same source (day 0 yw female). Bracket indicates mean ±SD. p-values from Student’s t-test is shown. (F) Effect of X and Y chromosome inheritance from young vs. old parents on nucleolar morphology, as a percentage of total GSCs scored (n, number of GSCs scored). P-value from chi-squared test is shown.

Figure 4—source data 1. Pixel intensity measurement and its ratio from DNA FISH plotted in Figure 4E.
DOI: 10.7554/eLife.32421.009