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本文引用的文献

1
Many X-linked microRNAs escape meiotic sex chromosome inactivation.许多X连锁的微小RNA逃避减数分裂性染色体失活。
Nat Genet. 2009 Apr;41(4):488-93. doi: 10.1038/ng.338. Epub 2009 Mar 22.
2
X chromosome inactivation in the absence of Dicer.在缺乏Dicer的情况下X染色体失活
Proc Natl Acad Sci U S A. 2009 Jan 27;106(4):1122-7. doi: 10.1073/pnas.0812210106. Epub 2009 Jan 21.
3
X-chromosome inactivation: the molecular basis of silencing.X染色体失活:沉默的分子基础。
J Biol. 2008 Oct 27;7(8):30. doi: 10.1186/jbiol95.
4
Intersection of the RNA interference and X-inactivation pathways.RNA干扰与X染色体失活途径的交叉
Science. 2008 Jun 6;320(5881):1336-41. doi: 10.1126/science.1157676.
5
Telomeres acquire distinct heterochromatin characteristics during siRNA-induced RNA interference in mouse cells.在小鼠细胞中,端粒在小干扰RNA(siRNA)诱导的RNA干扰过程中获得独特的异染色质特征。
Curr Biol. 2008 Feb 12;18(3):183-7. doi: 10.1016/j.cub.2007.12.059.
6
miRNA and piRNA localization in the male mammalian meiotic nucleus.微小RNA和Piwi相互作用RNA在雄性哺乳动物减数分裂细胞核中的定位
Chromosome Res. 2008;16(2):243-60. doi: 10.1007/s10577-007-1190-6. Epub 2008 Jan 22.
7
Trimethylation of histone H3 lysine 4 is an epigenetic mark at regions escaping mammalian X inactivation.组蛋白H3赖氨酸4的三甲基化是哺乳动物X染色体失活逃逸区域的一种表观遗传标记。
Epigenetics. 2007 Apr-Jun;2(2):114-8. doi: 10.4161/epi.2.2.4612. Epub 2007 Jun 1.
8
Cloning and expression profiling of testis-expressed microRNAs.睾丸表达的微小RNA的克隆与表达谱分析
Dev Biol. 2007 Nov 15;311(2):592-602. doi: 10.1016/j.ydbio.2007.09.009. Epub 2007 Sep 18.
9
X inactivation Xplained.X染色体失活解析
Curr Opin Genet Dev. 2007 Oct;17(5):387-93. doi: 10.1016/j.gde.2007.08.001. Epub 2007 Sep 14.
10
Meiotic silencing and the epigenetics of sex.减数分裂沉默与性别的表观遗传学。
Chromosome Res. 2007;15(5):633-51. doi: 10.1007/s10577-007-1143-0.

性染色体失活在男性中。

Sex chromosome inactivation in the male.

机构信息

Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV, USA.

出版信息

Epigenetics. 2009 Oct 1;4(7):452-6. doi: 10.4161/epi.4.7.9923. Epub 2009 Oct 25.

DOI:10.4161/epi.4.7.9923
PMID:19838052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3052906/
Abstract

Mammalian females have two X chromosomes, while males have only one X plus a Y chromosome. In order to balance X-linked gene dosage between the sexes, one X chromosome undergoes inactivation during development of female embryos. This process has been termed X-chromosome inactivation (XCI). Inactivation of the single X chromosome also occurs in the male, but is transient and is confined to the late stages of first meiotic prophase during spermatogenesis. This phenomenon has been termed meiotic sex chromosome inactivation (MSCI). A substantial portion ( approximately 15-25%) of X-linked mRNA-encoding genes escapes XCI in female somatic cells. While no mRNA genes are known to escape MSCI in males, approximately 80% of X-linked miRNA genes have been shown to escape this process. Recent results have led to the proposal that the RNA interference mechanism may be involved in regulating XCI in female cells. We suggest that some MSCI-escaping miRNAs may play a similar role in regulating MSCI in male germ cells.

摘要

哺乳动物的女性有两条 X 染色体,而男性只有一条 X 染色体加上一条 Y 染色体。为了平衡性别之间的 X 连锁基因剂量,女性胚胎发育过程中会有一条 X 染色体失活。这个过程被称为 X 染色体失活(XCI)。男性的单条 X 染色体也会失活,但这种失活是短暂的,仅限于精子发生过程中第一次减数分裂前期的晚期。这种现象被称为减数分裂性染色体失活(MSCI)。在女性体细胞中,大量(约 15-25%)的 X 连锁编码 mRNA 的基因逃避 XCI。虽然在男性中没有已知的 mRNA 基因逃避 MSCI,但约 80%的 X 连锁 miRNA 基因已被证明逃避了这一过程。最近的研究结果表明,RNA 干扰机制可能参与调节女性细胞中的 XCI。我们提出,一些逃避 MSCI 的 miRNA 可能在调节男性生殖细胞中的 MSCI 中发挥类似的作用。