Changing subcellular localization of nuclear transport factors during human spermatogenesis

P. A. F. Whiley, Y. Miyamoto, R. I. McLachlan, D. A. Jans, K. L. Loveland
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引用次数: 23

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.

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人类精子发生过程中核转运因子亚细胞定位的改变
精子发生需要激素和局部因素介导的基因表达的进行性变化。在整个配子体发生过程中,细胞核和细胞质间调节的大分子运动使这些对细胞外信号变化的基本反应,以及核细胞质转运蛋白和输入蛋白的动态产生,使它们成为种系分化的关键介质。我们检测了正常成人睾丸中六种进口蛋白和另外五种参与核细胞质运输的蛋白的表达谱。虽然α4在种系分化过程中主要存在于细胞核中,但只存在于支持细胞和生殖细胞的细胞质中。圆形精细胞核中存在多种蛋白(进口蛋白α1、α3、β1、β3;输出蛋白1、Nup62、Ran、RanBP1、RCC1)和输入蛋白α1、输入蛋白α3和Nup62在精母细胞中检测到强烈的核和/或核相关信号。本研究确定了精子发生过程中核细胞质运输的保守方面,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,在精母细胞中输入α3是核的,而输出α 1是细胞质的,这表明核转运在减数分裂过程中发生了改变。
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200
审稿时长
6-12 weeks
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