Lee Jibak, Iwai Toshiharu, Yokota Takehiro, Yamashita Masakane
Laboratory of Molecular and Cellular Interactions, Division of Biological Sciences, Graduate School of Science, Hokkaido University, Sapporo 060-0810, Japan.
J Cell Sci. 2003 Jul 1;116(Pt 13):2781-90. doi: 10.1242/jcs.00495. Epub 2003 May 20.
Sister chromatid cohesion is maintained from DNA replication to metaphase-to-anaphase transition by multisubunit protein complexes called cohesin, which include at least four proteins, SMC1alpha, SMC3, Rad21 and either SA1 or SA2, in mammalian somatic cells. We report here the first evidence of the involvement of Rec8 protein, a mammalian homolog of yeast Rec8p, in meiosis-specific chromosome behavior in mammals. In immunoblotting and immunohistochemical analysis using specific antibodies against mouse Rec8, we found that Rec8 was expressed in the testis but not in the kidney or liver; more precisely, it was expressed in spermatocytes and spermatids but not in spermatogonia or other somatic cells. We also found that Rec8 is present in both phosphorylated and dephosphorylated states in vivo. Immunoprecipitation analyses revealed that Rec8 associates with other cohesin proteins, SMC1beta (meiosis-specific protein) and SMC3 and with a component of synaptonemal complexes, SCP3, but not with SMC1alpha. In meiotic chromosome spreads, Rec8 was localized along the axial/lateral elements of the synaptonemal complexes in meiotic prophase from the leptotene to diplotene stages. At later stages, diakinesis and metaphase I, Rec8 was localized along the interstitial axes of chromosomes, including both centromere and arm regions of chromosomes. However, concomitantly with separation of homologous chromosomes in anaphase I, Rec8 was no longer detected along the arm regions, while it persisted on centromere regions up to metaphase II. In anaphase II, the centromeric signals were diminished. We propose from these results that mammalian Rec8 protein, in association with SMC3 and SMC1beta but not SMC1alpha, is involved in meiosis-specific chromosome behavior, and that homologous chromosome separation is triggered by selective loss of Rec8 from chromosome arms in meiosis I, while sister chromatid cohesion is maintained until metaphase II/anaphase II transition by centromeric Rec8 during mammalian meiosis.
在哺乳动物体细胞中,姐妹染色单体黏连通过名为黏连蛋白的多亚基蛋白复合体得以维持,从DNA复制到中期至后期的转变,黏连蛋白至少包含四种蛋白质,即SMC1α、SMC3、Rad21以及SA1或SA2。我们在此报告了Rec8蛋白(酵母Rec8p的哺乳动物同源物)参与哺乳动物减数分裂特异性染色体行为的首个证据。在使用针对小鼠Rec8的特异性抗体进行的免疫印迹和免疫组织化学分析中,我们发现Rec8在睾丸中表达,但在肾脏或肝脏中不表达;更确切地说,它在精母细胞和精子细胞中表达,但在精原细胞或其他体细胞中不表达。我们还发现Rec8在体内以磷酸化和去磷酸化两种状态存在。免疫沉淀分析表明,Rec8与其他黏连蛋白、SMC1β(减数分裂特异性蛋白)和SMC3以及联会复合体的一个组分SCP3相关联,但与SMC1α不相关。在减数分裂染色体铺展中,Rec8在减数分裂前期从细线期到双线期阶段沿着联会复合体的轴向/侧向元件定位。在后期,即终变期和减数第一次分裂中期,Rec8沿着染色体的间质轴定位,包括染色体的着丝粒和臂区域。然而,随着同源染色体在减数第一次分裂后期分离,在臂区域不再检测到Rec8,而它在着丝粒区域持续存在直至减数第二次分裂中期。在减数第二次分裂后期,着丝粒信号减弱。基于这些结果,我们提出哺乳动物Rec8蛋白与SMC3和SMC1β而非SMC1α相关联,参与减数分裂特异性染色体行为,并且同源染色体分离是由减数第一次分裂中染色体臂上Rec8的选择性缺失触发的,而姐妹染色单体黏连在哺乳动物减数分裂期间通过着丝粒Rec8维持到减数第二次分裂中期/后期转变。