Hyun Moonjung, Bohr Vilhelm A, Ahn Byungchan
Department of Life Sciences, University of Ulsan, Ulsan 680749, Korea.
Biochemistry. 2008 Jul 15;47(28):7583-93. doi: 10.1021/bi800197m. Epub 2008 Jun 18.
The highly conserved RecQ helicases are essential for the maintenance of genomic stability. Werner syndrome protein, WRN, is one of five human RecQ helicase homologues, and a deficiency of the protein causes a hereditary premature aging disorder that is characterized by genomic instability. A WRN orthologue, wrn-1 lacking the exonuclease domain, has been identified in the nematode Caenorhabditis elegans. wrn-1(RNAi) in C. elegans has a shortened life span, increased sensitivity to DNA damage, and accelerated aging phenotypes. However, little is known about its enzymatic activity. We purified the recombinant C. elegans WRN-1 protein (CeWRN-1) and then investigated its substrate specificity in vitro to improve our understanding of its function in vivo. We found that CeWRN-1 is an ATP-dependent 3'-5' helicase capable of unwinding a variety of DNA structures such as forked duplexes, Holliday junctions, bubble substrates, D-loops, and flap duplexes, and 3'-tailed duplex substrates. Distinctly, CeWRN-1 is able to unwind a long forked duplex compared to human WRN. Furthermore, CeWRN-1 helicase activity on a long DNA duplex is stimulated by C. elegans replication protein A (CeRPA) that is shown to interact with CeWRN-1 by a dot blot. The ability of CeWRN-1 to unwind these DNA structures may improve the access for DNA repair and replication proteins that are important for preventing the accumulation of abnormal structures, contributing to genomic stability.
高度保守的RecQ解旋酶对于维持基因组稳定性至关重要。沃纳综合征蛋白(WRN)是人类五种RecQ解旋酶同源物之一,该蛋白的缺乏会导致一种遗传性早衰疾病,其特征为基因组不稳定。在秀丽隐杆线虫中已鉴定出一种WRN直系同源物wrn-1,它缺乏核酸外切酶结构域。秀丽隐杆线虫中的wrn-1(RNA干扰)具有寿命缩短、对DNA损伤敏感性增加以及加速衰老的表型。然而,对其酶活性了解甚少。我们纯化了重组秀丽隐杆线虫WRN-1蛋白(CeWRN-1),然后在体外研究其底物特异性,以增进我们对其体内功能的理解。我们发现CeWRN-1是一种依赖ATP的3'-5'解旋酶,能够解开多种DNA结构,如叉状双链体、霍利迪连接体、气泡底物、D环和瓣状双链体以及3'尾双链底物。明显的是,与人类WRN相比,CeWRN-1能够解开较长的叉状双链体。此外,秀丽隐杆线虫复制蛋白A(CeRPA)刺激CeWRN-1在长DNA双链体上的解旋酶活性,斑点印迹显示CeRPA与CeWRN-1相互作用。CeWRN-1解开这些DNA结构的能力可能会改善对DNA修复和复制蛋白的可及性,这些蛋白对于防止异常结构的积累很重要,有助于基因组稳定性。