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染色体定位与男性不育:与生俱来的问题。

Chromosome positioning and male infertility: it comes with the territory.

机构信息

Genetics of Male Fertility Group. Unitat de Biologia Cel·lular. Departament de Biologia Cel·lular, Fisiologia i Immunologia. Facultat de Biociències, Universitat Autònoma de Barcelona, Bellaterra, 08193, Cerdanyola del Vallès, Spain.

出版信息

J Assist Reprod Genet. 2018 Nov;35(11):1929-1938. doi: 10.1007/s10815-018-1313-3. Epub 2018 Sep 18.

Abstract

The production of functional spermatozoa through spermatogenesis requires a spatially and temporally highly regulated gene expression pattern, which in case of alterations, leads to male infertility. Changes of gene expression by chromosome anomalies, gene variants, and epigenetic alterations have been described as the main genetic causes of male infertility. Recent molecular and cytogenetic approaches have revealed that higher order chromosome positioning is essential for basic genome functions, including gene expression. This review addresses this issue by exposing well-founded evidences which support that alterations on the chromosome topology in spermatogenetic cells leads to defective sperm function and could be considered as an additional genetic cause of male infertility.

摘要

通过精子发生产生功能性精子需要空间和时间上高度调控的基因表达模式,而这种模式发生改变会导致男性不育。染色体异常、基因突变和表观遗传改变导致的基因表达变化被认为是男性不育的主要遗传原因。最近的分子和细胞遗传学方法表明,高级别的染色体定位对于包括基因表达在内的基本基因组功能是必需的。这篇综述通过揭示有力的证据来解决这个问题,这些证据支持在精原细胞中染色体拓扑结构的改变导致精子功能缺陷,并可被视为男性不育的另一个遗传原因。

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