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对双性基因的分子分析,双性基因是一种控制黑腹果蝇雄性和雌性性别分化的双功能基因。

A molecular analysis of doublesex, a bifunctional gene that controls both male and female sexual differentiation in Drosophila melanogaster.

作者信息

Baker B S, Wolfner M F

机构信息

Department of Biology, University of California, San Diego, La Jolla 92093.

出版信息

Genes Dev. 1988 Apr;2(4):477-89. doi: 10.1101/gad.2.4.477.

Abstract

The doublesex (dsx) gene regulates somatic sexual differentiation in both sexes in Drosophila melanogaster. dsx has active but opposite negative regulatory functions in males and females. In males, the dsx locus represses the genes responsible for female sexual differentiation; male differentiation functions, not being repressed, are expressed. Conversely, in females, the dsx locus represses the genes involved in male sexual differentiation and the female sexual differentiation functions, not being repressed, are expressed. We have molecularly cloned the dsx locus by chromosomal walking and localized the gene within the cloned region by determining the positions of breakpoints of chromosomal rearrangements broken in dsx and in closely flanking regions. The dsx locus is about 40 kb in size. Its DNA is unique and appears to be organized in the same way in genomes of males and females. There is a developmentally and sexually regulated set of transcripts produced by the dsx locus. During the larval period, two sex-nonspecific dsx transcripts are produced. At the end of the larval period, these transcripts disappear and are replaced by a set of male-specific and female-specific transcripts. In adults, an additional male-specific transcript appears. Because genetic analysis has shown that transcription of the dsx locus must occur during the pupal period for proper sexual differentiation, we infer that the sex-specific transcripts seen during the pupal period correspond to the sex determination regulatory functions defined by mutational analysis. The regulation of dsx expression and possible roles of the other dsx transcripts are discussed.

摘要

双性基因(doublesex,dsx)调控黑腹果蝇两性的体细胞性分化。dsx在雄性和雌性中具有活跃但相反的负调控功能。在雄性中,dsx位点抑制负责雌性性分化的基因;而未被抑制的雄性分化功能得以表达。相反,在雌性中,dsx位点抑制参与雄性性分化的基因,未被抑制的雌性性分化功能得以表达。我们通过染色体步移对dsx位点进行了分子克隆,并通过确定在dsx及其紧邻区域发生断裂的染色体重排断点位置,将该基因定位在克隆区域内。dsx位点大小约为40 kb。其DNA是独特的,在雄性和雌性基因组中的组织方式似乎相同。dsx位点产生一组受发育和性别调控的转录本。在幼虫期,产生两种性别非特异性的dsx转录本。在幼虫期末期,这些转录本消失,并被一组雄性特异性和雌性特异性转录本所取代。在成虫中,出现了一种额外的雄性特异性转录本。由于遗传分析表明,dsx位点的转录必须在蛹期发生才能实现正常的性分化,我们推断在蛹期看到的性别特异性转录本对应于通过突变分析定义的性别决定调控功能。本文还讨论了dsx表达的调控以及其他dsx转录本可能的作用。

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