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EMSY 过表达破坏 DNA 损伤反应中的 BRCA2/RAD51 通路:作为检查点疾病的染色体不稳定性/重组综合征的意义。

EMSY overexpression disrupts the BRCA2/RAD51 pathway in the DNA-damage response: implications for chromosomal instability/recombination syndromes as checkpoint diseases.

机构信息

Department of Microbiology and Immunology, Faculty of Medicine, Université de Montréal, Montréal, QC, Canada.

出版信息

Mol Genet Genomics. 2011 Apr;285(4):325-40. doi: 10.1007/s00438-011-0612-5. Epub 2011 Mar 16.

Abstract

EMSY links the BRCA2 pathway to sporadic breast/ovarian cancer. It encodes a nuclear protein that binds to the BRCA2 N-terminal domain implicated in chromatin/transcription regulation, but when sporadically amplified/overexpressed, increased EMSY level represses BRCA2 transactivation potential and induces chromosomal instability, mimicking the activity of BRCA2 mutations in the development of hereditary breast/ovarian cancer. In addition to chromatin/transcription regulation, EMSY may also play a role in the DNA-damage response, suggested by its ability to localize at chromatin sites of DNA damage/repair. This implies that EMSY overexpression may also repress BRCA2 in DNA-damage replication/checkpoint and recombination/repair, coordinated processes that also require its interacting proteins: PALB2, the partner and localizer of BRCA2; RPA, replication/checkpoint protein A; and RAD51, the inseparable recombination/repair enzyme. Here, using a well-characterized recombination/repair assay system, we demonstrate that a slight increase in EMSY level can indeed repress these two processes independently of transcriptional interference/repression. Since EMSY, RPA and PALB2 all bind to the same BRCA2 region, these findings further support a scenario wherein: (a) EMSY amplification may mimic BRCA2 deficiency, at least by overriding RPA and PALB2, crippling the BRCA2/RAD51 complex at DNA-damage and replication/transcription sites; and (b) BRCA2/RAD51 may coordinate these processes by employing at least EMSY, PALB2 and RPA. We extensively discuss the molecular details of how this can happen to ascertain its implications for a novel recombination mechanism apparently conceived as checkpoint rather than a DNA repair system for cell division, survival, death, and human diseases, including the tissue specificity of cancer predisposition, which may renew our thinking about targeted therapy and prevention.

摘要

EMSY 将 BRCA2 通路与散发性乳腺癌/卵巢癌联系起来。它编码一种核蛋白,与 BRCA2 N 端结构域结合,该结构域涉及染色质/转录调控,但当散发性扩增/过表达时,增加的 EMSY 水平会抑制 BRCA2 转录激活潜能并诱导染色体不稳定性,类似于 BRCA2 突变在遗传性乳腺癌/卵巢癌发展中的作用。除了染色质/转录调控外,EMSY 还可能在 DNA 损伤反应中发挥作用,这表明它能够定位于 DNA 损伤/修复的染色质部位。这意味着 EMSY 过表达也可能在 DNA 损伤复制/检查点和重组/修复中抑制 BRCA2,这些协调过程也需要其相互作用蛋白:BRCA2 的伴侣和定位蛋白 PALB2、复制/检查点蛋白 A(RPA)和不可分割的重组/修复酶 RAD51。在这里,我们使用经过充分验证的重组/修复检测系统,证明 EMSY 水平的轻微增加确实可以独立于转录干扰/抑制来抑制这两个过程。由于 EMSY、RPA 和 PALB2 都结合到相同的 BRCA2 区域,这些发现进一步支持了这样一种情况:(a)EMSY 扩增可能模拟 BRCA2 缺陷,至少通过超越 RPA 和 PALB2,使 BRCA2/RAD51 复合物在 DNA 损伤和复制/转录部位失效;(b)BRCA2/RAD51 可能通过至少利用 EMSY、PALB2 和 RPA 来协调这些过程。我们广泛讨论了这种情况发生的分子细节,以确定其对一种新型重组机制的影响,这种机制显然被视为检查点,而不是用于细胞分裂、存活、死亡和人类疾病(包括癌症易感性的组织特异性)的 DNA 修复系统,这可能会重新思考靶向治疗和预防。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ff/3064890/4d1d01c6a9b0/438_2011_612_Fig1_HTML.jpg

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