Whitby M C
Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Biochem Soc Trans. 2005 Dec;33(Pt 6):1451-5. doi: 10.1042/BST0331451.
Homologous recombination (HR) is required to promote both correct chromosome segregation and genetic variation during meiosis. For this to be successful recombination intermediates must be resolved to generate reciprocal exchanges or 'crossovers' between the homologous chromosomes (homologues) during the first meiotic division. Crossover recombination promotes faithful chromosome segregation by establishing connections (chiasmata) between the homologues, which help guide their proper bipolar alignment on the meiotic spindle. Recent studies of meiotic recombination in both the budding and fission yeasts have established that there are at least two pathways for generating crossovers. One pathway involves the resolution of fully ligated four-way DNA junctions [HJs (Holliday junctions)] by an as yet unidentified endonuclease. The second pathway appears to involve the cleavage of the precursors of ligated HJs, namely displacement (D) loops and unligated/nicked HJs, by the Mus81-Eme1/Mms4 endonuclease.
在减数分裂过程中,同源重组(HR)对于促进正确的染色体分离和遗传变异都是必需的。为了使这一过程成功,重组中间体必须得到解决,以便在第一次减数分裂期间在同源染色体(同源物)之间产生相互交换或“交叉”。交叉重组通过在同源物之间建立连接(交叉)来促进忠实的染色体分离,这有助于引导它们在减数分裂纺锤体上正确的双极排列。最近对芽殖酵母和裂殖酵母减数分裂重组的研究表明,至少有两条产生交叉的途径。一条途径涉及由一种尚未确定的核酸内切酶对完全连接的四链DNA连接点[HJs(霍利迪连接点)]进行拆分。第二条途径似乎涉及由Mus81-Eme1/Mms4核酸内切酶切割连接的HJs的前体,即置换(D)环和未连接/有切口的HJs。