Kurdzo Emily L, Obeso David, Chuong Hoa, Dawson Dean S
Program in Cell Cycle and Cancer Biology, Oklahoma Medical Research Foundation, Oklahoma 73104.
Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma 73104.
Genetics. 2017 Feb;205(2):657-671. doi: 10.1534/genetics.116.190264. Epub 2016 Dec 2.
In meiosis I, chromosomes become paired with their homologous partners and then are pulled toward opposite poles of the spindle. In the budding yeast, Saccharomyces cerevisiae, in early meiotic prophase, centromeres are observed to associate in pairs in a homology-independent manner; a process called centromere coupling. Later, as homologous chromosomes align, their centromeres associate in a process called centromere pairing. The synaptonemal complex protein Zip1 is necessary for both types of centromere association. We aimed to test the role of centromere coupling in modulating recombination at centromeres, and to test whether the two types of centromere associations depend upon the same sets of genes. The zip1-S75E mutation, which blocks centromere coupling but no other known functions of Zip1, was used to show that in the absence of centromere coupling, centromere-proximal recombination was unchanged. Further, this mutation did not diminish centromere pairing, demonstrating that these two processes have different genetic requirements. In addition, we tested other synaptonemal complex components, Ecm11 and Zip4, for their contributions to centromere pairing. ECM11 was dispensable for centromere pairing and segregation of achiasmate partner chromosomes; while ZIP4 was not required for centromere pairing during pachytene, but was required for proper segregation of achiasmate chromosomes. These findings help differentiate the two mechanisms that allow centromeres to interact in meiotic prophase, and illustrate that centromere pairing, which was previously shown to be necessary to ensure disjunction of achiasmate chromosomes, is not sufficient for ensuring their disjunction.
在减数分裂I中,染色体与其同源配对物配对,然后被拉向纺锤体的两极。在出芽酵母酿酒酵母中,在减数分裂前期早期,着丝粒以同源独立的方式成对结合;这个过程称为着丝粒偶联。后来,随着同源染色体排列,它们的着丝粒在一个称为着丝粒配对的过程中结合。联会复合体蛋白Zip1对于这两种着丝粒结合都是必需的。我们旨在测试着丝粒偶联在调节着丝粒处重组中的作用,并测试这两种着丝粒结合是否依赖于相同的基因集。zip1-S75E突变阻断了着丝粒偶联,但不影响Zip1的其他已知功能,该突变用于表明在没有着丝粒偶联的情况下,着丝粒近端重组没有变化。此外,这种突变并没有减少着丝粒配对,表明这两个过程有不同的遗传需求。另外,我们测试了其他联会复合体成分Ecm11和Zip4对着丝粒配对的贡献。Ecm11对于着丝粒配对和无交叉配对染色体的分离是可有可无的;而ZIP4在粗线期对着丝粒配对不是必需的,但对于无交叉染色体的正确分离是必需的。这些发现有助于区分减数分裂前期着丝粒相互作用的两种机制,并表明着丝粒配对虽然先前已证明对确保无交叉染色体的分离是必要的,但不足以确保它们的分离。