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).