Mankouri Hocine W, Hickson Ian D
Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Trends Biochem Sci. 2007 Dec;32(12):538-46. doi: 10.1016/j.tibs.2007.09.009. Epub 2007 Nov 5.
RecQ helicases, together with topoisomerase III and Rmi1 family proteins, form an evolutionarily conserved complex that is essential for the maintenance of genome integrity. This complex, which we term RTR, is capable of, or has been implicated in, the processing of a diverse array of DNA structures, and we propose here that it functions in a coordinated fashion as a DNA structure-specific 'dissolvasome'. Little is known about how the RTR complex might be regulated or targeted to various DNA structures in vivo. Recent findings indicate that the components of the RTR complex might activate the cell cycle checkpoint machinery as well as be a target of checkpoint kinases, suggesting that these events are crucial to ensure faithful DNA replication and chromosome segregation.
RecQ解旋酶与拓扑异构酶III和Rmi1家族蛋白一起,形成一个进化上保守的复合体,该复合体对于维持基因组完整性至关重要。我们将这个复合体称为RTR,它能够或已被认为与多种DNA结构的处理有关,并且我们在此提出它以协调的方式作为一种DNA结构特异性的“溶解体”发挥作用。关于RTR复合体在体内如何被调控或靶向各种DNA结构,人们知之甚少。最近的研究结果表明,RTR复合体的组分可能激活细胞周期检查点机制,同时也是检查点激酶的作用靶点,这表明这些事件对于确保准确的DNA复制和染色体分离至关重要。