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血管生成素和核糖核酸酶 4 的转录受 RNA 聚合酶 III 元件和一个依赖于 CCCTC 结合因子(CTCF)的内含子染色质环调控。

Transcription of angiogenin and ribonuclease 4 is regulated by RNA polymerase III elements and a CCCTC binding factor (CTCF)-dependent intragenic chromatin loop.

机构信息

From the Molecular Oncology Research Institute, Tufts Medical Center, Boston, Massachusetts 02111 and.

出版信息

J Biol Chem. 2014 May 2;289(18):12520-34. doi: 10.1074/jbc.M114.551762. Epub 2014 Mar 21.

Abstract

Angiogenin (ANG) and ribonuclease 4 (RNASE4), two members of the secreted and vertebrate-specific ribonuclease superfamily, play important roles in cancers and neurodegenerative diseases. The ANG and RNASE4 genes share genetic regions with promoter activities, but the structure and regulation of these putative promotes are unknown. We have characterized the promoter regions, defined the transcription start site, and identified a mechanism of transcription regulation that involves both RNA polymerase III (Pol III) elements and CCCTC binding factor (CTCF) sites. We found that two Pol III elements within the promoter region influence ANG and RNASE4 expression in a position- and orientation-dependent manner. We also provide evidence for the presence of an intragenic chromatin loop between the two CTCF binding sites located in two introns flanking the ANG coding exon. We found that formation of this intragenic loop preferentially enhances ANG transcription. These results suggest a multilayer transcriptional regulation of ANG and RNASE4 gene locus. These data also add more direct evidence to the notion that Pol III elements are able to directly influence Pol II gene transcription. Furthermore, our data indicate that a CTCF-dependent chromatin loop is able to differentially regulate transcription of genes that share the same promoters.

摘要

血管生成素 (ANG) 和核糖核酸酶 4 (RNASE4) 是分泌型和脊椎动物特异性核糖核酸酶超家族的两个成员,在癌症和神经退行性疾病中发挥重要作用。ANG 和 RNASE4 基因与具有启动子活性的遗传区域共享,但这些假定启动子的结构和调节尚不清楚。我们已经对启动子区域进行了表征,定义了转录起始位点,并确定了一种转录调节机制,该机制涉及 RNA 聚合酶 III (Pol III) 元件和 CCCTC 结合因子 (CTCF) 位点。我们发现启动子区域内的两个 Pol III 元件以位置和取向依赖的方式影响 ANG 和 RNASE4 的表达。我们还提供了证据,证明位于侧翼 ANG 编码外显子的两个内含子中的两个 CTCF 结合位点之间存在基因内染色质环。我们发现这种基因内环的形成优先增强 ANG 转录。这些结果表明 ANG 和 RNASE4 基因座存在多层次转录调控。这些数据还为 Pol III 元件能够直接影响 Pol II 基因转录的观点提供了更多直接证据。此外,我们的数据表明,CTCF 依赖性染色质环能够差异调节共享相同启动子的基因的转录。

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