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. 2008 Jan;178(1):235–243. doi: 10.1534/genetics.107.083212

TABLE 2.

% P-Ser5
% P-Ser2
Transgene % lethality N None Low High N None Positive N
PIE-1(1–335) 9 701 0 100 0 15 87 13 105
PIE-1(1–355) cdk-7(RNAi) 96 422 100 0 0 42 100 0 42
PIE-1(1–335) cit-1.1/1.2(RNAi) 91 408 4 96 0 51 100 0 40
PIE-1(1–335) ama-1(RNAi) 97 445 100 0 0 51 100 0 45
PIE-1(1–240) 100 1038 0 0 100 25 0 100 151
PIE-1(1–240) cdk-7(RNAi) 100 441 100 0 0 46 100 0 45
PIE-1(1–240) cit-1.1/1.2(RNAi) 100 446 0 0 100 44 100 0 29
PIE-1(1–240) ama-1(RNAi) 100 364 100 0 0 45 100 0 43

Control RNAi experiments to evaluate the specificity of the P-Ser5 and P-Ser2 signals in pie-1(zu127) embryos carrying the indicated transgenes. P-Ser5 levels are divided into three categories depending on whether P-Ser5 was detected at levels equivalent to that seen in somatic blastomeres (high), at the intermediate level typical of wild-type germline blastomeres (low, with two prominent foci), or absent (none) (also see Figure 2). As expected for a modification linked to initiation, P-Ser5 signals (both in the high and low categories) are eliminated upon depletion of cdk-7 and ama-1, but remain unaffected by depletion cit-1.1/1.2. In contrast, as expected for a modification linked to elongation, P-Ser2 signals are eliminated upon depletion of all three genes.

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