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How two helicases work together within the TFIIH complex, a perspective from structural studies of XPB and XPD helicases
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作者 Li FAN 《Frontiers in Biology》 CAS CSCD 2013年第4期363-368,共6页
Xeroderma pigmentosum group B (XPB) and D (XPD) are two DNA helicases inside the transcription factor TFIIH complex required for both transcription and DNA repair. The importance of these helicases is underscored ... Xeroderma pigmentosum group B (XPB) and D (XPD) are two DNA helicases inside the transcription factor TFIIH complex required for both transcription and DNA repair. The importance of these helicases is underscored by the fact that mutations of XPB and XPD cause diseases with extremely high sensitivity to UV-light and high risk of cancer, premature aging, etc. This mini-review focuses on recent developments in both structural and functional characterization of these XP heficases to illustrate their distinguished biological roles within the architectural restriction of the TFIIH complex. In particular, molecular mechanisms of DNA unwinding by these helicases for promoter opening during transcription initiation and bubble-creation around the lesion during DNA repair are described based on the integration of the crystal structures of XPB and XPD helicases into the architecture of the TFIIH complex. 展开更多
关键词 XPB XPD tfiih HELICASE DNA repair nucleotide excision repair Wanscription
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人XPB基因在核苷酸剪切修复和基因转录中的分子机制
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作者 胡晓东 张吉翔 《细胞生物学杂志》 CSCD 2005年第3期291-294,共4页
核苷酸剪切修复(NER)途径是维持生物体基因组稳定的重要机制。人着色性干皮病B组(xerodermapigmentosumgroupB,XPB)基因又名ERCC3基因,它既是NER途径不可缺少的成员又是转录因子TFIIH的最大p89亚基。它是具有从3'端→5'端依赖AT... 核苷酸剪切修复(NER)途径是维持生物体基因组稳定的重要机制。人着色性干皮病B组(xerodermapigmentosumgroupB,XPB)基因又名ERCC3基因,它既是NER途径不可缺少的成员又是转录因子TFIIH的最大p89亚基。它是具有从3'端→5'端依赖ATP的单链DNA解旋酶活性的蛋白质,执行依赖DNA的ATP酶和解旋酶功能,在损伤DNA修复和基因转录中均起重要作用,并将两者有机偶联。该基因突变将导致3种不同的遗传疾病:着色性干皮病(xerodermapigmentosum,XP),科凯恩氏综合征(cockayne’ssyndrome,CS),毛发硫营养不良(trichothiodystrophy,TTD)。其基因型通过在DNA修复和转录中的功能与表型联系起来。另外,XPB与p53存在物理和功能上的相互作用。现从XPB的3个方面即“一个基因,两种功能,3种疾病”作一综述。 展开更多
关键词 人XPB基因 核苷酸剪切修复 基因转录 分子机制 DNA修复 tfiih因子 基因突变 疾病 结构
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