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精子发生中的基因调控。

Gene regulation in spermatogenesis.

作者信息

Maclean James A, Wilkinson Miles F

机构信息

Department of Immunology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Curr Top Dev Biol. 2005;71:131-97. doi: 10.1016/S0070-2153(05)71005-X.

Abstract

Mammalian spermatogenesis is a complex hormone-dependent developmental program in which a myriad of events must take place to ensure that germ cells reach their proper stage of development at the proper time. Many of these events are controlled by cell type- and stage-specific transcription factors. The regulatory mechanisms involved provide an intriguing paradigm for the field of developmental biology and may lead to the development of new contraceptives an and innovative routs to treat male infertility. In this review, we address three aspects of the genetic regulatory mechanism that drive spermatogenesis. First, we detail what is known about how steroid hormones (both androgens and estrogens) and their cognate receptors initiate and maintain mammalian spermatogenesis. Steroids act through three mechanistic routes: (i) direct activation of genes through hormone-dependent promoter elements, (ii) secondary transcriptional responses through activation of hormone-dependent transcription factors, and (iii) rapid, transcription-independent (nonclassical) events induced by steroid hormones. Second, we provide a survey of transcription factors that function in mammalian spermatogenesis, including homeobox, zinc-finger, heat-shock, and cAMP-response family members. Our survey is not intended to cover all examples but to give a flavor for the gamut of biological roles conferred by transcription factors in the testis, particularly those defined in knockout mice. Third, we address how testis-specific transcription is achieved. In particular, we cover the evidence for and against the idea that some testis-specific genes are transcriptionally silent in somatic tissues as a result of DNA methylation.

摘要

哺乳动物精子发生是一个复杂的激素依赖性发育程序,其中必须发生无数事件以确保生殖细胞在适当时间达到其适当的发育阶段。这些事件中的许多由细胞类型和阶段特异性转录因子控制。所涉及的调控机制为发育生物学领域提供了一个引人入胜的范例,并可能导致新型避孕药的开发以及治疗男性不育症的创新途径。在本综述中,我们探讨了驱动精子发生的遗传调控机制的三个方面。首先,我们详细阐述了类固醇激素(雄激素和雌激素)及其同源受体如何启动和维持哺乳动物精子发生的已知情况。类固醇通过三种机制途径起作用:(i)通过激素依赖性启动子元件直接激活基因,(ii)通过激活激素依赖性转录因子产生二级转录反应,以及(iii)由类固醇激素诱导的快速、不依赖转录(非经典)事件。其次,我们概述了在哺乳动物精子发生中起作用的转录因子,包括同源框、锌指、热休克和cAMP反应家族成员。我们的概述并非旨在涵盖所有例子,而是为转录因子在睾丸中赋予的一系列生物学作用提供一个概览,特别是那些在基因敲除小鼠中定义的作用。第三,我们探讨了如何实现睾丸特异性转录。特别是,我们涵盖了支持和反对某些睾丸特异性基因由于DNA甲基化而在体细胞组织中处于转录沉默状态这一观点的证据。

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