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染色质机制在基因组印记中的作用。

Chromatin mechanisms in genomic imprinting.

机构信息

CNRS and University of Montpellier I and II, Montpellier, France.

出版信息

Mamm Genome. 2009 Sep-Oct;20(9-10):544-56. doi: 10.1007/s00335-009-9223-4. Epub 2009 Sep 17.

Abstract

Mammalian imprinted genes are clustered in chromosomal domains. Their mono-allelic, parent-of-origin-specific expression is regulated by imprinting control regions (ICRs), which are essential sequence elements marked by DNA methylation on one of the two parental alleles. These methylation "imprints" are established during gametogenesis and, after fertilization, are somatically maintained throughout development. Nonhistone proteins and histone modifications contribute to this epigenetic process. The way ICRs mediate imprinted gene expression differs between domains. At some domains, for instance, ICRs produce long noncoding RNAs that mediate chromatin silencing. Lysine methylation on histone H3 is involved in this developmental process and is particularly important for imprinting in the placenta and brain. Together, the newly discovered chromatin mechanisms provide further clues for addressing imprinting-related pathologies in humans.

摘要

哺乳动物印迹基因簇位于染色体区域内。其单等位基因、亲本来源特异性表达受印迹控制区(ICR)调控,ICR 是由两条亲本等位基因之一上的 DNA 甲基化标记的必需序列元件。这些甲基化“印迹”在配子发生过程中建立,受精后,在整个发育过程中通过体细胞维持。非组蛋白和组蛋白修饰有助于这一表观遗传过程。ICR 介导印迹基因表达的方式在不同区域有所不同。例如,在一些区域,ICR 产生长非编码 RNA,介导染色质沉默。组蛋白 H3 上的赖氨酸甲基化参与了这一发育过程,对胎盘和大脑中的印迹尤为重要。新发现的染色质机制共同为解决人类印迹相关疾病提供了进一步的线索。

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