Ding Da-Qiao, Matsuda Atsushi, Okamasa Kasumi, Nagahama Yuki, Haraguchi Tokuko, Hiraoka Yasushi
Advanced ICT Research Institute Kobe, National Institute of Information and Communications Technology, 588-2 Iwaoka, Iwaoka-cho Nishi-ku, Kobe, 651-2492, Japan.
Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, 565-0871, Japan.
Chromosoma. 2016 Jun;125(2):205-14. doi: 10.1007/s00412-015-0551-8. Epub 2015 Oct 28.
Chromosome structure is dramatically altered upon entering meiosis to establish chromosomal architectures necessary for the successful progression of meiosis-specific events. An early meiotic event involves the replacement of the non-SMC mitotic cohesins with their meiotic equivalents in most part of the chromosome, forming an axis on meiotic chromosomes. We previously demonstrated that the meiotic cohesin complex is required for chromosome compaction during meiotic prophase in the fission yeast Schizosaccharomyces pombe. These studies revealed that chromosomes are elongated in the absence of the meiotic cohesin subunit Rec8 and shortened in the absence of the cohesin-associated protein Pds5. In this study, using super-resolution structured illumination microscopy, we found that Rec8 forms a linear axis on chromosomes, which is required for the organized axial structure of chromatin during meiotic prophase. In the absence of Pds5, the Rec8 axis is shortened whereas chromosomes are widened. In rec8 or pds5 mutants, the frequency of homologous chromosome pairing is reduced. Thus, Rec8 and Pds5 play an essential role in building a platform to support the chromosome architecture necessary for the spatial alignment of homologous chromosomes.
进入减数分裂时,染色体结构会发生显著改变,以建立减数分裂特异性事件成功进行所必需的染色体结构。减数分裂早期事件包括在染色体的大部分区域用减数分裂等同物取代非SMC有丝分裂黏连蛋白,从而在减数分裂染色体上形成一个轴。我们之前证明,在裂殖酵母粟酒裂殖酵母中,减数分裂黏连蛋白复合体是减数分裂前期染色体压缩所必需的。这些研究表明,在没有减数分裂黏连蛋白亚基Rec8的情况下,染色体伸长,而在没有黏连蛋白相关蛋白Pds5的情况下,染色体缩短。在本研究中,我们使用超分辨率结构照明显微镜发现,Rec8在染色体上形成一个线性轴,这是减数分裂前期染色质有组织的轴向结构所必需的。在没有Pds5的情况下,Rec8轴缩短而染色体变宽。在rec8或pds5突变体中,同源染色体配对频率降低。因此,Rec8和Pds5在构建一个支持同源染色体空间排列所必需的染色体结构的平台中发挥着重要作用。