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人类精子发生过程中核转运因子亚细胞定位的变化

Changing subcellular localization of nuclear transport factors during human spermatogenesis.

作者信息

Whiley P A F, Miyamoto Y, McLachlan R I, Jans D A, Loveland K L

机构信息

Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australia.

出版信息

Int J Androl. 2012 Apr;35(2):158-69. doi: 10.1111/j.1365-2605.2011.01202.x. Epub 2011 Aug 4.

Abstract

Spermatogenesis requires progressive changes in gene expression mediated by hormonal and local factors. Regulated macromolecular movement between nuclear and cytoplasmic compartments enables these essential responses to changing extracellular cues, and dynamic production of the nucleocytoplasmic transporters and importin proteins, throughout gametogenesis in rodents implicates them as key mediators of germline differentiation. We examined normal adult human testis expression profiles of six importins plus five additional proteins involved in nucleocytoplasmic transport. Although most were detected in the nucleus during germline differentiation, importin α4 was exclusively observed in Sertoli and germ cell cytoplasm. Many proteins were present in round spermatid nuclei (importins α1, α3, β1, β3; exportin-1, Nup62, Ran, RanBP1, RCC1), and remarkable intense nuclear and/or nuclear-associated signals were detected for importin α1, importin α3 and Nup62 in spermatocytes. This study identifies conserved aspects of nucleocytoplasmic transport during spermatogenesis and extends our knowledge of the dynamic presence of these proteins, which indicates that they contribute to germ cell-specific cargo trafficking and potentially to other functions during human spermatogenesis. We also demonstrate for the first time that importin α3 is nuclear in spermatocytes, when exportin-1 is cytoplasmic, suggesting that nuclear transport is altered during meiosis.

摘要

精子发生需要由激素和局部因素介导的基因表达的渐进性变化。核与细胞质区室之间受调控的大分子运动使这些细胞能够对不断变化的细胞外信号做出必要反应,并且在啮齿动物的整个配子发生过程中,核质转运蛋白和输入蛋白的动态产生表明它们是生殖系分化的关键介质。我们检测了六种输入蛋白以及另外五种参与核质运输的蛋白质在正常成人睾丸中的表达谱。尽管大多数在生殖系分化过程中在细胞核中被检测到,但输入蛋白α4仅在支持细胞和生殖细胞的细胞质中被观察到。许多蛋白质存在于圆形精子细胞核中(输入蛋白α1、α3、β1、β3;输出蛋白-1、核孔蛋白62、Ran、Ran结合蛋白1、RCC1),并且在精母细胞中检测到输入蛋白α1、输入蛋白α3和核孔蛋白62有明显强烈的核和/或核相关信号。这项研究确定了精子发生过程中核质运输的保守方面,并扩展了我们对这些蛋白质动态存在的认识,这表明它们有助于生殖细胞特异性货物运输,并可能在人类精子发生过程中发挥其他功能。我们还首次证明,当输出蛋白-1在细胞质中时,输入蛋白α3在精母细胞中位于细胞核内,这表明减数分裂期间核运输发生了改变。

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