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在雄性生殖细胞中诱导雌性性致死基因RNA剪接:对果蝇生殖系性别决定的影响

Induction of female Sex-lethal RNA splicing in male germ cells: implications for Drosophila germline sex determination.

作者信息

Hager J H, Cline T W

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley 94720-3204, USA.

出版信息

Development. 1997 Dec;124(24):5033-48. doi: 10.1242/dev.124.24.5033.

Abstract

With a focus on Sex-lethal (Sxl), the master regulator of Drosophila somatic sex determination, we compare the sex determination mechanism that operates in the germline with that in the soma. In both cell types, Sxl is functional in females (2X2A) and nonfunctional in males (1X2A). Somatic cell sex is determined initially by a dose effect of X:A numerator genes on Sxl transcription. Once initiated, the active state of SXL is maintained by a positive autoregulatory feedback loop in which Sxl protein insures its continued synthesis by binding to Sxl pre-mRNA and thereby imposing the productive (female) splicing mode. The gene splicing-necessary factor (snf), which encodes a component of U1 and U2 snRNPs, participates in this RNA splicing control. Here we show that an increase in the dose of snf+ can trigger the female Sxl RNA splicing mode in male germ cells and can feminize triploid intersex (2X3A) germ cells. These snf+ dose effects are as dramatic as those of X:A numerator genes on Sxl in the soma and qualify snf as a numerator element of the X:A signal for Sxl in the germline. We also show that female-specific regulation of Sxl in the germline involves a positive autoregulatory feedback loop on RNA splicing, as it does in the soma. Neither a phenotypically female gonadal soma nor a female dose of X chromosomes in the germline is essential for the operation of this feedback loop, although a female X-chromosome dose in the germline may facilitate it. Engagement of the Sxl splicing feedback loop in somatic cells invariably imposes female development. In contrast, engagement of the Sxl feedback loop in male germ cells does not invariably disrupt spermatogenesis; nevertheless, it is premature to conclude that Sxl is not a switch gene in germ cells for at least some sex-specific aspects of their differentiation. Ironically, the testis may be an excellent organ in which to study the interactions among regulatory genes such as Sxl, snf, ovo and otu which control female-specific processes in the ovary.

摘要

以果蝇体细胞性别决定的主要调节因子性致死基因(Sex-lethal,Sxl)为重点,我们比较了生殖系和体细胞中运行的性别决定机制。在这两种细胞类型中,Sxl在雌性(2X2A)中发挥功能,而在雄性(1X2A)中无功能。体细胞性别最初由X:A分子基因对Sxl转录的剂量效应决定。一旦启动,SXL的活性状态通过正自调节反馈环得以维持,在该反馈环中,Sxl蛋白通过与Sxl前体mRNA结合来确保其持续合成,从而强制形成有效的(雌性)剪接模式。编码U1和U2小核核糖核蛋白(snRNP)组分的基因剪接必需因子(snf)参与这种RNA剪接控制。在此我们表明,snf+剂量的增加可在雄性生殖细胞中触发雌性Sxl RNA剪接模式,并可使三倍体雌雄间性(2X3A)生殖细胞雌性化。这些snf+剂量效应与X:A分子基因对体细胞中Sxl的效应一样显著,使snf成为生殖系中Sxl的X:A信号的分子元件。我们还表明,生殖系中Sxl的雌性特异性调节涉及RNA剪接的正自调节反馈环,体细胞中也是如此。尽管生殖系中的雌性X染色体剂量可能会促进该反馈环的运行,但表型为雌性的性腺体细胞或生殖系中雌性剂量的X染色体对于该反馈环的运行并非必不可少。Sxl剪接反馈环在体细胞中的参与总是会导致雌性发育。相比之下,Sxl反馈环在雄性生殖细胞中的参与并不总是会破坏精子发生;然而,现在就得出Sxl在生殖细胞中对于其分化的至少某些性别特异性方面不是开关基因的结论还为时过早。具有讽刺意味的是,睾丸可能是研究诸如Sxl、snf、ovo和otu等控制卵巢中雌性特异性过程的调节基因之间相互作用的绝佳器官。

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