Salz H K
Department of Genetics, Case Western Reserve University, Cleveland, Ohio 44106.
Genetics. 1992 Mar;130(3):547-54. doi: 10.1093/genetics/130.3.547.
Our analysis demonstrates that snf is a positive regulator of Sex-lethal in both the germline and the soma. In the germline, unregulated expression of Sex-lethal can bypass the requirement for snf+ gene function, implying that snf is required for Sex-lethal activity in the germline. This conclusion is supported by the finding that the Sex-lethal transcription pattern is abnormal in a snf mutant background. In the soma, activation of Sex-lethal appears to be sensitive to snf gene dosage only when the probability of Sex-lethal activation has been otherwise reduced. We also show that the activity of one of the constitutive Sex-lethal alleles (SxlM1) is sensitive to snf gene dosage, demonstrating that, in spite of its constitutive behavior in some assays, SxlM1 is still subject to some regulation. In spite of snf's role in the somatic activation of Sex-lethal, no lethal alleles of snf were isolated in a screen of approximately 25,000 chromosomes. The observation that the existing snf mutations present a lethal phenotype only in certain genetic backgrounds suggests that snf is required, but is not essential, for the activation of Sex-lethal in the soma. In contrast, snf does appear to be essential for activation of Sex-lethal in the germline, as evidenced by its female-sterile phenotype.
我们的分析表明,snf在生殖系和体细胞中都是性致死基因(Sex-lethal)的正向调节因子。在生殖系中,性致死基因不受调控的表达可以绕过对snf+基因功能的需求,这意味着snf是生殖系中性致死基因活性所必需的。这一结论得到了以下发现的支持:在snf突变背景下,性致死基因的转录模式是异常的。在体细胞中,只有当性致死基因激活的概率已通过其他方式降低时,性致死基因的激活才似乎对snf基因剂量敏感。我们还表明,组成型性致死基因等位基因之一(SxlM1)的活性对snf基因剂量敏感,这表明,尽管它在某些测定中表现出组成型行为,但SxlM1仍然受到一些调控。尽管snf在性致死基因的体细胞激活中起作用,但在对约25000条染色体的筛选中未分离到snf的致死等位基因。现有snf突变仅在某些遗传背景下呈现致死表型这一观察结果表明,snf是体细胞中性致死基因激活所必需的,但不是必不可少的。相比之下,snf似乎对生殖系中性致死基因的激活至关重要,这一点从其雌性不育表型中可以得到证明。