Schnabel R, Weigner C, Hutter H, Feichtinger R, Schnabel H
Max-Planck-Institut für Biochemie, Martinsried, Germany.
Mech Dev. 1996 Feb;54(2):133-47. doi: 10.1016/0925-4773(95)00466-1.
It is thought that at least some of the initial specification of the five somatic founder cells of the C. elegans embryo occurs cell-autonomously through the segregation of factors during cell divisions. It has been suggested that in embryos from mothers homozygous for mutations in the maternal-effect gene mex-1, four blastomeres of the 8-cell embryo adopt the fate of the MS blastomere. It was proposed that mex-1 functions to localise or regulate factors that determine the fate of this blastomere. Here, a detailed cell lineage analysis of 9 mex-1 mutants reveals that the fates of all somatic founder cells are affected by mutations in this gene. We propose that mex-1, like the par genes, is involved in establishing the initial polarity of the embryo.
人们认为,秀丽隐杆线虫胚胎的五个体细胞奠基细胞的至少一些初始特化是通过细胞分裂过程中因子的分离而自主发生的。有人提出,在母源效应基因mex-1发生突变的纯合子母亲的胚胎中,8细胞胚胎的四个卵裂球会采用MS卵裂球的命运。有人提出,mex-1的功能是定位或调节决定该卵裂球命运的因子。在这里,对9个mex-1突变体进行的详细细胞谱系分析表明,所有体细胞奠基细胞的命运都受到该基因突变的影响。我们提出,mex-1与par基因一样,参与建立胚胎的初始极性。