转录因子ⅡH
解旋酶
Cockayne综合征
生物
核苷酸切除修复
色素性干皮病
转录因子ⅡA
一般转录因子
遗传学
转录因子
抄写(语言学)
DNA修复
细胞生物学
DNA
发起人
核糖核酸
基因
语言学
哲学
基因表达
作者
Olga Kolesnikova,Laura Radu,Arnaud Poterszman
出处
期刊:Advances in protein chemistry and structural biology
日期:2019-01-01
卷期号:: 21-67
被引量:45
标识
DOI:10.1016/bs.apcsb.2019.01.003
摘要
Transcription factor IIH (TFIIH) is a multiprotein complex involved in both eukaryotic transcription and DNA repair, revealing a tight connection between these two processes. Composed of 10 subunits, it can be resolved into a 7-subunits core complex with the XPB translocase and the XPD helicase, and the 3-subunits kinase complex CAK, which also exists as a free complex with a distinct function. Initially identified as basal transcription factor, TFIIH also participates in transcription regulation and plays a key role in nucleotide excision repair (NER) for opening DNA at damaged sites, lesion verification and recruitment of additional repair factors. Our understanding of TFIIH function in eukaryotic cells has greatly benefited from studies of the genetic rare diseases xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD), that are not only characterized by cancer and aging predispositions but also by neurological and developmental defects. Although much remains unknown about TFIIH function, significant progresses have been done regarding the structure of the complex, the functions of its catalytic subunits and the multiple roles of the regulatory core-TFIIH subunits. This review provides a non-exhaustive survey of key discoveries on the structure and function of this pivotal factor, which can be considered as a promising target for therapeutic strategies.
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