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Kcnq1ot1 非编码 RNA 通过与 Dnmt1 相互作用介导转录基因沉默。

Kcnq1ot1 noncoding RNA mediates transcriptional gene silencing by interacting with Dnmt1.

机构信息

Department of Genetics and Pathology, Dag Hammarskjölds Väg 20, 75185 Rudbeck Laboratory, Uppsala University, Uppsala 75185, Sweden.

出版信息

Development. 2010 Aug 1;137(15):2493-9. doi: 10.1242/dev.048181. Epub 2010 Jun 23.

Abstract

A long noncoding RNA, Kcnq1ot1, regulates the expression of both ubiquitously and tissue-specific imprinted genes within the Kcnq1 domain. However, the functional sequences of the Kcnq1ot1 RNA that mediate lineage-specific imprinting are unknown. Here, we have generated a knockout mouse with a deletion encompassing an 890-bp silencing domain (Delta890) downstream of the Kcnq1ot1 promoter. Maternal transmission of the Delta890 allele has no effect on imprinting, whereas paternal inheritance of the deletion leads to selective relaxation of the imprinting of ubiquitously imprinted genes to a variable extent in a tissue-specific manner. Interestingly, the deletion affects DNA methylation at somatically acquired differentially methylated regions (DMRs), but does not affect the histone modifications of the ubiquitously imprinted genes. Importantly, we found that Kcnq1ot1 recruits Dnmt1 to somatic DMRs by interacting with Dnmt1, and that this interaction was significantly reduced in the Delta890 mice. Thus, the ubiquitous and placental-specific imprinting of genes within the Kcnq1 domain might be mediated by distinct mechanisms, and Kcnq1ot1 RNA might mediate the silencing of ubiquitously imprinted genes by maintaining allele-specific methylation through its interactions with Dnmt1.

摘要

一个长的非编码 RNA,Kcnq1ot1,调节着 Kcnq1 结构域内的广泛表达和组织特异性印记基因的表达。然而,介导谱系特异性印记的 Kcnq1ot1 RNA 的功能序列尚不清楚。在这里,我们生成了一种敲除小鼠,该小鼠缺失了 Kcnq1ot1 启动子下游的一个 890bp 的沉默结构域(Delta890)。Delta890 等位基因的母系传递对印记没有影响,而缺失的父系遗传导致广泛印记基因的印记在组织特异性方式下以可变的程度选择性松弛。有趣的是,缺失影响了体细胞获得的差异甲基化区域(DMRs)的 DNA 甲基化,但不影响广泛印记基因的组蛋白修饰。重要的是,我们发现 Kcnq1ot1 通过与 Dnmt1 相互作用将 Dnmt1 募集到体细胞 DMRs,而在 Delta890 小鼠中这种相互作用显著减少。因此,Kcnq1 结构域内基因的广泛表达和胎盘特异性印记可能由不同的机制介导,而 Kcnq1ot1 RNA 可能通过与 Dnmt1 的相互作用维持等位基因特异性甲基化,从而介导广泛印记基因的沉默。

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