Fig. 2: Separating wGDe inheritance by F2 sex allows different mechanisms of inheritance bias to be distinguished.
From: A CRISPR endonuclease gene drive reveals distinct mechanisms of inheritance bias

a Illustration of how homing, meiotic drive and copy-grafting/co-conversion are expected to influence the observed sex-linkage of an M (shown in Blue) linked wGDe element in the progeny of male drive double heterozygous parents. The expected sex-linkage is exactly opposite for an m linked wGDe element. b Parental germline inheritance bias of wGDe when combined with no Cas9, nup50, bgcn, or an sds3-Cas9 expressing element. We included the nup50 results from Li et al. that use the identical wGDe and nup50-Cas9 line. For each of the three Cas9 regulatory elements, the wGDe inheritance from male double heterozygotes is reported in pairs of columns segregated by the sex of the F2 progeny. In each case, the first pair of columns are the results for when wGDe is m-linked (m), and the second pair are the results for when wGDe is M-linked (M). Data are presented as mean values with the Wilson confidence intervals for the binomial proportion calculated for the pooled progeny count. The overlaid numbers are the percentage (cumulative within each column) of the indicated F2 sex and wGDe status among all progeny from that cross. The number of progeny scored is presented in Supplementary Table S3. Source data are provided as a Source Data file.