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

TABLE 1.

Transgene % lethality n % P-Ser5 (high) n % P-Ser2 n
No transgene 100 >50 100 >50 100 >50
PIE-1(1–335) 9 701 0 15 13 105
PIE-1(1–320) 3 1002 0 25 7 92
PIE-1(1–299) 11 298 0 25 5 50
PIE-1(1–279) 100 623 100 25 97 67
PIE-1(1–259) 100 346 ND ND 100 25
PIE-1(1–240) 100 1038 100 25 100 151
PIE-1(DAQMEQT) 8 829 0 30 82 165
PIE-1(ΔYAPMAPT) 8 934 0 39 89 54
PIE-1(Δ240–259) 62 634 52 25 94 74

Percentage of pie-1(zu127) embryos expressing the indicated transgene that did not survive embryogenesis (% lethality), that exhibited a germline blastomere with high P-Ser5 levels (equivalent to somatic blastomeres) (% P-Ser5), or that exhibited a germline blastomere positive for P-Ser2 (% P-Ser2) is shown. Italics indicate no rescue of the pie-1(zu127) phenotypes, underlining indicates partial rescue, and no italics or underlining indicates rescue comparable to that obtained with the wild-type transgene PIE-1(1–335). Note that rescued embryos no longer have high P-Ser5 levels (equivalent to somatic blastomeres), but maintain the low intermediate levels observed in wild-type germline blastomeres (Figure 2). Examination of digital images revealed that, for the majority of pie-1(zu127) embryos expressing PIE-1(DAQMEQT) (16/20) and PIE-1(ΔYAPMAPT) (18/21), P-Ser2 levels in germline blastomeres were equivalent to P-Ser2 levels in somatic blastomeres (also see Figure 2).

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