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H19 lincRNA 是 miR-675 的发育储库,可抑制生长和 Igf1r。

The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1r.

机构信息

Epigenetics Programme, Babraham Institute, Cambridge, CB22 3AT, UK.

出版信息

Nat Cell Biol. 2012 Jun 10;14(7):659-65. doi: 10.1038/ncb2521.

Abstract

The H19 large intergenic non-coding RNA (lincRNA) is one of the most highly abundant and conserved transcripts in mammalian development, being expressed in both embryonic and extra-embryonic cell lineages, yet its physiological function is unknown. Here we show that miR-675, a microRNA (miRNA) embedded in H19's first exon, is expressed exclusively in the placenta from the gestational time point when placental growth normally ceases, and placentas that lack H19 continue to grow. Overexpression of miR-675 in a range of embryonic and extra-embryonic cell lines results in their reduced proliferation; targets of the miRNA are upregulated in the H19 null placenta, including the growth-promoting insulin-like growth factor 1 receptor (Igf1r) gene. Moreover, the excision of miR-675 from H19 is dynamically regulated by the stress-response RNA-binding protein HuR. These results suggest that H19's main physiological role is in limiting growth of the placenta before birth, by regulated processing of miR-675. The controlled release of miR-675 from H19 may also allow rapid inhibition of cell proliferation in response to cellular stress or oncogenic signals.

摘要

H19 长基因间非编码 RNA(lincRNA) 是哺乳动物发育过程中丰度最高且最保守的转录本之一,在胚胎和胚胎外细胞谱系中均有表达,但它的生理功能尚不清楚。在这里,我们发现 miR-675 是一种嵌入 H19 第一外显子的 microRNA(miRNA),仅在胎盘生长正常停止的妊娠时间点从胎盘表达,并且缺乏 H19 的胎盘继续生长。miR-675 在一系列胚胎和胚胎外细胞系中的过表达导致其增殖减少;miRNA 的靶基因在 H19 缺失的胎盘中上调,包括促进生长的胰岛素样生长因子 1 受体 (Igf1r) 基因。此外,miR-675 从 H19 中的切除受到应激反应 RNA 结合蛋白 HuR 的动态调节。这些结果表明,H19 的主要生理作用是通过调节 miR-675 的加工来限制出生前胎盘的生长。miR-675 从 H19 的受控释放也可能允许在细胞应激或致癌信号下快速抑制细胞增殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bca/3389517/9fa7dc0356df/ukmss-48289-f0001.jpg

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