Oliver B, Perrimon N, Mahowald A P
Department of Developmental Genetics and Anatomy, Case Western Reserve University, School of Medicine, Cleveland, Ohio 44106.
Genes Dev. 1987 Nov;1(9):913-23. doi: 10.1101/gad.1.9.913.
Mutations at the ovo locus result in a defective female germ line. The male germ line is not affected. Adult females homozygous for loss-of-function alleles have no germ line stem cells. The sex-specific phenotype is evident at late blastoderm and early gastrula stages when the pole cells of embryos homozygous for a loss-of-function allele begin to die. This is the only zygotically acting gene known that is required specifically for embryonic germ line survival. Females heterozygous for dominant alleles or homozygous for alleles reducing gene activity exhibit a range of defects in oogenesis. We have mapped the ovo locus to position 4E1-2 of the salivary gland X chromosome by using a set of cytologically visible deletions.
ovo位点的突变会导致雌性生殖系出现缺陷。雄性生殖系不受影响。功能丧失等位基因的纯合成年雌性没有生殖系干细胞。当功能丧失等位基因的纯合胚胎的极细胞开始死亡时,这种性别特异性表型在胚盘后期和原肠胚早期很明显。这是已知的唯一一种专门用于胚胎生殖系存活的合子作用基因。显性等位基因的杂合雌性或基因活性降低的等位基因的纯合雌性在卵子发生过程中表现出一系列缺陷。我们通过使用一组细胞学上可见的缺失,将ovo位点定位到唾液腺X染色体的4E1-2位置。