Mello C C, Schubert C, Draper B, Zhang W, Lobel R, Priess J R
Department of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98104, USA.
Nature. 1996 Aug 22;382(6593):710-2. doi: 10.1038/382710a0.
Totipotent germline blastomeres in Caenorhabditis elegans contain, but do not respond to, factors that promote somatic differentiation in other embryonic cells. Mutations in the maternal gene pie-1 result in the germline blastomeres adopting somatic cell fates. Here we show that pie-1 encodes a nuclear protein, PIE-1, that is localized to the germline blastomeres throughout early development. During division of each germline blastomere, PIE-1 initially associates with both centrosomes of the mitotic spindle. However, PIE-1 rapidly disappears from the centrosome destined for the somatic daughter, and persists in the centrosome of the daughter that becomes the next germline blastomere. The PIE-1 protein contains potential zinc-finger motifs also found in the mammalian growth-factor response protein TIS-11/NUP475 (refs 4-7). The localization and genetic properties of pie-1 provide an example of a repressor-based mechanism for preserving pluripotency within a stem cell lineage.
秀丽隐杆线虫中的全能生殖系卵裂球含有促进其他胚胎细胞体细胞分化的因子,但对这些因子没有反应。母源基因pie-1的突变导致生殖系卵裂球采用体细胞命运。我们在此表明,pie-1编码一种核蛋白PIE-1,该蛋白在早期发育过程中定位于生殖系卵裂球。在每个生殖系卵裂球分裂期间,PIE-1最初与有丝分裂纺锤体的两个中心体结合。然而,PIE-1迅速从注定形成体细胞后代的中心体消失,并持续存在于成为下一个生殖系卵裂球的后代的中心体中。PIE-1蛋白含有在哺乳动物生长因子反应蛋白TIS-11/NUP475中也发现的潜在锌指基序(参考文献4-7)。pie-1的定位和遗传特性提供了一种基于阻遏物的机制的例子,用于在干细胞谱系中维持多能性。