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层流切应力调节内皮型一氧化氮合酶基因的 RNA 聚合酶 II 的磷酸化和定位。

Laminar shear stress modulates phosphorylation and localization of RNA polymerase II on the endothelial nitric oxide synthase gene.

机构信息

1639 Pierce Drive, WMB 319, Atlanta, GA 30322, USA.

出版信息

Arterioscler Thromb Vasc Biol. 2010 Mar;30(3):561-7. doi: 10.1161/ATVBAHA.109.199554.

Abstract

OBJECTIVE

In endothelial cells exposed to unidirectional laminar shear stress, endothelial nitric oxide synthase transcription (eNOS), mRNA stability, and protein levels are enhanced. We have previously demonstrated that these changes are associated with increased 3' polyadenylation of eNOS mRNA. Here, we investigated the effect of laminar shear stress on the phosphorylation and localization of RNA polymerase (Pol) II, the enzyme primarily responsible for coordinating transcription and posttranscriptional processing.

METHODS AND RESULTS

Using Western and chromatin immunoprecipitation analyses, Pol II phosphorylation and localization on the eNOS gene were assessed in bovine aortic endothelial cells exposed to laminar shear stress. Total Pol II (phosphorylated and unphosphorylated) levels were increased 65% in response to laminar shear stress. This was associated with an increase in Pol II phosphoserine 2, but no change in levels of the unphosphorylated or phosphoserine 5 isoforms. Quantitative chromatin immunoprecipitation analysis showed that laminar shear stress enhanced binding of Pol II phosphoserine 2 to the 3' end of the eNOS gene, particularly exon 26, which encodes the 3'UTR. Treatment of cells with DRB attenuated laminar shear stress-induced Pol II phosphorylation, eNOS 3' polyadenylation, and eNOS expression.

CONCLUSIONS

These data suggest that laminar shear stress enhances eNOS mRNA 3' polyadenylation by modulating phosphorylation and localization of Pol II.

摘要

目的

在暴露于单向层流剪切力的内皮细胞中,内皮型一氧化氮合酶转录(eNOS)、mRNA 稳定性和蛋白水平增强。我们之前已经证明,这些变化与 eNOS mRNA 的 3'多聚腺苷酸化增加有关。在这里,我们研究了层流剪切力对 RNA 聚合酶(Pol)II 磷酸化和定位的影响,Pol II 是主要负责协调转录和转录后加工的酶。

方法和结果

使用 Western 和染色质免疫沉淀分析,评估了暴露于层流剪切力的牛主动脉内皮细胞中 eNOS 基因上的 Pol II 磷酸化和定位。总 Pol II(磷酸化和非磷酸化)水平响应层流剪切力增加了 65%。这与 Pol II 磷酸丝氨酸 2 的增加有关,但未磷酸化或磷酸丝氨酸 5 同工型的水平没有变化。定量染色质免疫沉淀分析显示,层流剪切力增强了 Pol II 磷酸丝氨酸 2 与 eNOS 基因 3'端的结合,特别是编码 3'UTR 的外显子 26。用 DRB 处理细胞可减弱层流剪切力诱导的 Pol II 磷酸化、eNOS 3'多聚腺苷酸化和 eNOS 表达。

结论

这些数据表明,层流剪切力通过调节 Pol II 的磷酸化和定位来增强 eNOS mRNA 的 3'多聚腺苷酸化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30eb/2948754/57465b473897/nihms-172806-f0001.jpg

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