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转录偶联修复——作用机制、调控及相关人类疾病

Transcription-coupled repair - mechanisms of action, regulation, and associated human disorders.

作者信息

Nakazawa Yuka, Oka Yasuyoshi, Matsunaga Tomoko, Ogi Tomoo

机构信息

Department of Genetics, Research Institute of Environmental Medicine (RIeM), Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8601, Japan.

Department of Human Genetics and Molecular Biology, Nagoya University Graduate School of Medicine, 65, Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan.

出版信息

FEBS Lett. 2025 Jan;599(2):166-167. doi: 10.1002/1873-3468.15073. Epub 2024 Dec 20.

Abstract

The transcription-coupled repair (TCR) pathway resolves transcription-blocking DNA lesions to maintain cellular function and prevent transcriptional arrest. Stalled RNA polymerase II (RNAPII) triggers repair mechanisms, including RNAPII ubiquitination, which recruit UVSSA and TFIIH. Defects in TCR-associated genes cause disorders like Cockayne syndrome, UV-sensitive syndrome, xeroderma pigmentosum, and recently defined AMeDS. TCR safeguards transcription, linking its failure to neurodegeneration and disease phenotypes.

摘要

转录偶联修复(TCR)途径可解决转录阻断性DNA损伤,以维持细胞功能并防止转录停滞。停滞的RNA聚合酶II(RNAPII)触发修复机制,包括RNAPII泛素化,进而招募UVSSA和TFIIH。TCR相关基因的缺陷会导致诸如科凯恩综合征、紫外线敏感综合征、着色性干皮病以及最近定义的AMEDS等疾病。TCR保护转录,将其功能障碍与神经退行性变和疾病表型联系起来。

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