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PU.1 是肿瘤抑制基因 LIMD1 的主要转录激活因子。

PU.1 is a major transcriptional activator of the tumour suppressor gene LIMD1.

机构信息

School of Biomedical Sciences, University of Nottingham Medical School, Nottingham, UK.

出版信息

FEBS Lett. 2011 Apr 6;585(7):1089-96. doi: 10.1016/j.febslet.2011.03.013. Epub 2011 Mar 12.

Abstract

LIMD1 is a tumour suppressor gene (TSG) down regulated in ∼80% of lung cancers with loss also demonstrated in breast and head and neck squamous cell carcinomas. LIMD1 is also a candidate TSG in childhood acute lymphoblastic leukaemia. Mechanistically, LIMD1 interacts with pRB, repressing E2F-driven transcription as well as being a critical component of microRNA-mediated gene silencing. In this study we show a CpG island within the LIMD1 promoter contains a conserved binding motif for the transcription factor PU.1. Mutation of the PU.1 consensus reduced promoter driven transcription by 90%. ChIP and EMSA analysis demonstrated that PU.1 specifically binds to the LIMD1 promoter. siRNA depletion of PU.1 significantly reduced endogenous LIMD1 expression, demonstrating that PU.1 is a major transcriptional activator of LIMD1.

摘要

LIMD1 是一种肿瘤抑制基因(TSG),在约 80%的肺癌中下调,在乳腺癌和头颈部鳞状细胞癌中也有缺失的证据。LIMD1 也是儿童急性淋巴细胞白血病的候选 TSG。从机制上讲,LIMD1 与 pRB 相互作用,抑制 E2F 驱动的转录,同时也是 microRNA 介导的基因沉默的关键组成部分。在这项研究中,我们表明 LIMD1 启动子内的一个 CpG 岛含有转录因子 PU.1 的保守结合基序。PU.1 共有序列的突变使启动子驱动的转录减少了 90%。ChIP 和 EMSA 分析表明,PU.1 特异性地结合到 LIMD1 启动子上。PU.1 的 siRNA 耗竭显著降低了内源性 LIMD1 的表达,表明 PU.1 是 LIMD1 的主要转录激活因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f7/3078326/ca76070cb4ac/fx1.jpg

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