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果蝇中相对基因剂量与无女儿基因座复杂表型的关系。

The relationship of relative gene dose to the complex phenotype of the daughterless locus in Drosophila.

作者信息

Cronmiller C, Cline T W

机构信息

Department of Biology, Princeton University, NJ 08544.

出版信息

Dev Genet. 1986;7(4):205-21. doi: 10.1002/dvg.1020070406.

DOI:10.1002/dvg.1020070406
PMID:3453784
Abstract

The daughterless (da) gene provides an essential maternally supplied component for Drosophila sex determination and dosage compensation. In this connection, it is required as a positive regulator of a female-specific master regulatory gene, Sex-lethal (Sxl). In addition, zygotic da gene function is required for male and female viability. Thus, the phenotype da is complex; it includes both maternal and zygotic aspects, as well as both sex-specific and nonsex-specific aspects. Assessment of wild-type da function has relied on the characterization of only a single leaky mutant da allele. In order to better understand the nature of this allele and the relationships between the various aspects of its complex phenotype, tandem duplications of both the mutant and wild-type da alleles were isolated and used in a dose study of this gene's function. Three conclusions were reached: 1) by the most stringent genetic criteria, the mutant da allele is a simple hypomorph, an allele with reduced but non-zero levels of wild-type functions; 2) since increased dose of da+ had no effect on viability or progeny sex ratio, this gene seems not to be a dose-sensitive element of the X/A ratio sex determination signal; and 3) expression of the maternal da+ allele does make a contribution to the nonsex-specific developmental processes that require zygotic da+ function; however, that contribution is clearly minor. In contrast, the zygotic genotype with respect to da appears to have no effect on the expression of Sxl+ in the zygote, the sex-specific process that requires maternal da+ function.

摘要

无女儿基因(da)为果蝇性别决定和剂量补偿提供了一种必需的母体供应成分。就此而言,它是雌性特异性主调控基因性致死基因(Sxl)的正调控因子。此外,雄性和雌性的生存能力都需要合子型da基因的功能。因此,da的表型很复杂;它包括母体和合子方面,以及性别特异性和非性别特异性方面。对野生型da功能的评估仅依赖于对一个单一的渗漏突变da等位基因的表征。为了更好地理解这个等位基因的本质及其复杂表型各方面之间的关系,分离出了突变型和野生型da等位基因的串联重复,并用于该基因功能的剂量研究。得出了三个结论:1)按照最严格的遗传标准,突变型da等位基因是一个简单的亚效等位基因,即具有降低但非零水平的野生型功能的等位基因;2)由于增加da+的剂量对生存能力或后代性别比没有影响,该基因似乎不是X/A比性别决定信号的剂量敏感元件;3)母体da+等位基因的表达确实对需要合子型da+功能的非性别特异性发育过程有贡献;然而,这种贡献显然很小。相比之下,关于da的合子基因型似乎对合子中Sxl+的表达没有影响,而Sxl+的表达是需要母体da+功能的性别特异性过程。

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