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H19 编码区 5'端的 G-四链体结构调节 H19 转录。

A G-quadruplex structure at the 5' end of the H19 coding region regulates H19 transcription.

机构信息

Department of Biosystems Science, Institute for Frontier Life and Medical Science, Kyoto University, Sakyo-ku, Kyoto 606-8507, Japan.

Department of Mammalian Regulatory Network, Graduate School of Biostudies, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.

出版信息

Sci Rep. 2017 Apr 3;8:45815. doi: 10.1038/srep45815.

Abstract

The H19 gene, one of the best known imprinted genes, encodes a long non-coding RNA that regulates cell proliferation and differentiation. H19 RNA is widely expressed in embryonic tissues, but its expression is restricted in only a few tissues after birth. However, regulation of H19 gene expression remains poorly understood outside the context of genomic imprinting. Here we identified evolutionarily conserved guanine (G)-rich repeated motifs at the 5' end of the H19 coding region that are consistent with theoretically deduced G-quadruplex sequences. Circular dichroism spectroscopy and electrophoretic mobility shift assays with G-quadruplex-specific ligands revealed that the G-rich motif, located immediately downstream of the transcription start site (TSS), forms a G-quadruplex structure in vitro. By using a series of mutant forms of H19 harboring deletion or G-to-A substitutions, we found that the H19-G-quadruplex regulates H19 gene expression. We further showed that transcription factors Sp1 and E2F1 were associated with the H19-G-quadruplex to either suppress or promote the H19 transcription, respectively. Moreover, H19 expression during differentiation of mouse embryonic stem cells appears to be regulated by a genomic H19 G-quadruplex. These results demonstrate that the G-quadruplex structure immediately downstream of the TSS functions as a novel regulatory element for H19 gene expression.

摘要

H19 基因是最著名的印迹基因之一,编码一种长非编码 RNA,调节细胞增殖和分化。H19 RNA 在胚胎组织中广泛表达,但出生后仅在少数组织中表达。然而,在基因组印迹的背景之外,H19 基因表达的调节仍然知之甚少。在这里,我们在 H19 编码区的 5'端鉴定了进化上保守的富含鸟嘌呤(G)的重复基序,这些基序与理论上推断的 G-四链体序列一致。圆二色性光谱和具有 G-四链体特异性配体的电泳迁移率变动分析表明,富含 G 的基序位于转录起始位点(TSS)的下游,在体外形成 G-四链体结构。通过使用一系列携带缺失或 G 到 A 取代的 H19 突变形式,我们发现 H19-G-四链体调节 H19 基因表达。我们进一步表明,转录因子 Sp1 和 E2F1 与 H19-G-四链体结合,分别抑制或促进 H19 转录。此外,在小鼠胚胎干细胞分化过程中 H19 的表达似乎受到基因组 H19 G-四链体的调节。这些结果表明,TSS 下游的 G-四链体结构作为 H19 基因表达的新型调节元件发挥作用。

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