Houten Bennett Van, Kuper Jochen, Kisker Caroline
Department of Pharmacology and Chemical Biology, University of Pittsburgh Cancer Institute, University of Pittsburgh School of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, United States.
Rudolf-Virchow-Center for Experimental Biomedicine, University of Wuerzburg, Wuerzburg, Germany.
DNA Repair (Amst). 2016 Aug;44:136-142. doi: 10.1016/j.dnarep.2016.05.019. Epub 2016 May 16.
XPD, as part of the TFIIH complex, has classically been linked to the damage verification step of nucleotide excision repair (NER). However, recent data indicate that XPD, due to its iron-sulfur center interacts with the iron sulfur cluster assembly proteins, and may interact with other proteins in the cell to mediate a diverse set of biological functions including cell cycle regulation, mitosis, and mitochondrial function. In this perspective, after first reviewing the function and some of the key disease causing variants that affect XPD's interaction with TFIIH and the CDK-activating kinase complex (CAK), we investigate these intriguing cellular roles of XPD and highlight important unanswered questions that provide a fertile ground for further scientific exploration.
XPD作为TFIIH复合物的一部分,传统上一直与核苷酸切除修复(NER)的损伤验证步骤相关联。然而,最近的数据表明,XPD因其铁硫中心与铁硫簇组装蛋白相互作用,并且可能与细胞中的其他蛋白质相互作用,以介导包括细胞周期调控、有丝分裂和线粒体功能在内的多种生物学功能。从这个角度来看,在首先回顾了影响XPD与TFIIH和CDK激活激酶复合物(CAK)相互作用的功能以及一些关键的致病变体之后,我们研究了XPD这些有趣的细胞作用,并突出了重要的未解决问题,这些问题为进一步的科学探索提供了肥沃的土壤。