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C/EBPβ 介导 RNA 聚合酶 III 驱动的恶性神经胶质瘤中致癌 miRNA-138 的转录。

C/EBPβ mediates RNA polymerase III-driven transcription of oncomiR-138 in malignant gliomas.

机构信息

Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), Singapore 138648, Singapore.

Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

出版信息

Nucleic Acids Res. 2018 Jan 9;46(1):336-349. doi: 10.1093/nar/gkx1105.

Abstract

MicroRNA-138 (miR-138) is a pro-survival oncomiR for glioma stem cells. In malignant gliomas, dysregulated expression of microRNAs, such as miR-138, promotes Tumour initiation and progression. Here, we identify the ancillary role of the CCAAT/enhancer binding protein β (C/EBPβ) as a transcriptional activator of miR-138. We demonstrate that a short 158 bp DNA sequence encoding the precursor of miR-138-2 is essential and sufficient for transcription of miR-138. This short sequence includes the A-box and B-box elements characteristic of RNA Polymerase III (Pol III) promoters, and is also directly bound by C/EBPβ via an embedded 'C/EBPβ responsive element' (CRE). CRE and the Pol III B-box element overlap, suggesting that C/EBPβ and transcription factor 3C (TFIIIC) interact at the miR-138-2 locus. We propose that this interaction is essential for the recruitment of the RNA Pol III initiation complex and associated transcription of the oncomiR, miR-138 in malignant gliomas.

摘要

微小 RNA-138(miR-138)是神经胶质瘤干细胞的促生存致癌 miRNA。在恶性神经胶质瘤中,miR-138 等 microRNA 的失调表达促进了肿瘤的起始和进展。在这里,我们确定了 CCAAT/增强子结合蛋白β(C/EBPβ)作为 miR-138 的转录激活因子的辅助作用。我们证明,编码 miR-138-2 前体的 158 个碱基对的短 DNA 序列对于 miR-138 的转录是必需和充分的。该短序列包含 RNA 聚合酶 III(Pol III)启动子特有的 A 框和 B 框元件,并且还通过嵌入式“C/EBPβ 反应元件”(CRE)直接与 C/EBPβ 结合。CRE 和 Pol III B 框元件重叠,表明 C/EBPβ 和转录因子 3C(TFIIIC)在 miR-138-2 基因座上相互作用。我们提出,这种相互作用对于招募 RNA Pol III 起始复合物以及恶性神经胶质瘤中致癌 miRNA miR-138 的相关转录是必不可少的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a19e/5758869/bde75b67f465/gkx1105fig1.jpg

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