Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, CT, USA.
Adv Exp Med Biol. 2013;767:185-202. doi: 10.1007/978-1-4614-5037-5_9.
Homologous recombination (HR) is an evolutionarily conserved process that eliminates DNA double-strand breaks from chromosomes, repairs injured DNA replication forks, and helps orchestrate meiotic chromosome segregation. Recent studies have shown that DNA helicases play multifaceted roles in HR mediation and regulation. In particular, the S. cerevisiae Sgs1 helicase and its human ortholog BLM helicase are involved in not only the resection of the primary lesion to generate single-stranded DNA to prompt the assembly of the HR machinery, but they also function in somatic cells to suppress the formation of chromosome arm crossovers during HR. On the other hand, the S. cerevisiae Mph1 and Srs2 helicases, and their respective functional equivalents in other eukaryotes, suppress spurious HR events and favor the formation of noncrossovers via distinct mechanisms. Thus, the functional integrity of the HR process and HR outcomes are dependent upon these helicase enzymes. Since mutations in some of these helicases lead to cancer predisposition in humans and mice, studies on them have clear relevance to human health and disease.
同源重组(HR)是一种进化上保守的过程,可消除染色体上的 DNA 双链断裂,修复受损的 DNA 复制叉,并有助于协调减数分裂染色体分离。最近的研究表明,DNA 解旋酶在 HR 介导和调节中发挥着多方面的作用。特别是酿酒酵母 Sgs1 解旋酶及其人类同源物 BLM 解旋酶不仅参与原发性病变的切除以产生单链 DNA 以促使 HR 机制的组装,而且还在体细胞中发挥作用,以抑制 HR 过程中染色体臂交叉的形成。另一方面,酿酒酵母 Mph1 和 Srs2 解旋酶及其在其他真核生物中的相应功能等效物通过不同的机制抑制虚假的 HR 事件并有利于非交叉的形成。因此,HR 过程和 HR 结果的功能完整性取决于这些解旋酶酶。由于这些解旋酶中的一些突变会导致人类和小鼠易患癌症,因此对它们的研究与人类健康和疾病有明显的相关性。