Clouaire Thomas, Roussigne Myriam, Ecochard Vincent, Mathe Catherine, Amalric François, Girard Jean-Philippe
Laboratoire de Biologie Vasculaire, Equipe Labellisée La Ligue 2003, Institut de Pharmacologie et de Biologie Structurale, Centre National de la Recherche Scientifique Unité Mixte de Recherche 5089, 205 Route de Narbonne, 31077 Toulouse, France.
Proc Natl Acad Sci U S A. 2005 May 10;102(19):6907-12. doi: 10.1073/pnas.0406882102. Epub 2005 Apr 29.
We have recently described an evolutionarily conserved protein motif, designated the THAP domain, which defines a previously uncharacterized family of cellular factors (THAP proteins). The THAP domain exhibits similarities to the site-specific DNA-binding domain of Drosophila P element transposase, including a putative metal-coordinating C2CH signature (CX(2-4)CX(35-53)CX(2)H). In this article, we report a comprehensive list of approximately 100 distinct THAP proteins in model animal organisms, including human nuclear proapoptotic factors THAP1 and DAP4/THAP0, transcriptional repressor THAP7, zebrafish orthologue of cell cycle regulator E2F6, and Caenorhabditis elegans chromatin-associated protein HIM-17 and cell-cycle regulators LIN-36 and LIN-15B. In addition, we demonstrate the biochemical function of the THAP domain as a zinc-dependent sequence-specific DNA-binding domain belonging to the zinc-finger superfamily. In vitro binding-site selection allowed us to identify an 11-nucleotide consensus DNA-binding sequence specifically recognized by the THAP domain of human THAP1. Mutations of single nucleotide positions in this sequence abrogated THAP-domain binding. Experiments with the zinc chelator 1,10-o-phenanthroline revealed that the THAP domain is a zinc-dependent DNA-binding domain. Site-directed mutagenesis of single cysteine or histidine residues supported a role for the C2CH motif in zinc coordination and DNA-binding activity. The four other conserved residues (P, W, F, and P), which define the THAP consensus sequence, were also found to be required for DNA binding. Together with previous genetic data obtained in C. elegans, our results suggest that cellular THAP proteins may function as zinc-dependent sequence-specific DNA-binding factors with roles in proliferation, apoptosis, cell cycle, chromosome segregation, chromatin modification, and transcriptional regulation.
我们最近描述了一种进化上保守的蛋白质基序,命名为THAP结构域,它定义了一个以前未被表征的细胞因子家族(THAP蛋白)。THAP结构域与果蝇P元件转座酶的位点特异性DNA结合结构域具有相似性,包括一个推定的金属配位C2CH基序(CX(2 - 4)CX(35 - 53)CX(2)H)。在本文中,我们报告了模式动物中约100种不同THAP蛋白的综合列表,包括人类核促凋亡因子THAP1和DAP4/THAP0、转录抑制因子THAP7、细胞周期调节因子E2F6的斑马鱼直系同源物,以及秀丽隐杆线虫染色质相关蛋白HIM - 17和细胞周期调节因子LIN - 36和LIN - 15B。此外,我们证明了THAP结构域作为属于锌指超家族的锌依赖性序列特异性DNA结合结构域的生化功能。体外结合位点选择使我们能够鉴定出人类THAP1的THAP结构域特异性识别的11个核苷酸的共有DNA结合序列。该序列中单个核苷酸位置的突变消除了THAP结构域的结合。用锌螯合剂1,10 - 邻菲罗啉进行的实验表明,THAP结构域是锌依赖性DNA结合结构域。单个半胱氨酸或组氨酸残基的定点诱变支持了C2CH基序在锌配位和DNA结合活性中的作用。定义THAP共有序列的其他四个保守残基(P、W、F和P)也被发现是DNA结合所必需的。结合先前在秀丽隐杆线虫中获得的遗传数据,我们的结果表明,细胞内的THAP蛋白可能作为锌依赖性序列特异性DNA结合因子发挥作用,在增殖、凋亡、细胞周期、染色体分离、染色质修饰和转录调控中起作用。