Center for Reproductive Medicine, Women's and Children's Hospital, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Cell Death Dis. 2013 Aug 1;4(8):e749. doi: 10.1038/cddis.2013.269.
Chromatin structure and function are for a large part determined by the six members of the structural maintenance of chromosomes (SMC) protein family, which form three heterodimeric complexes: Smc1/3 (cohesin), Smc2/4 (condensin) and Smc5/6. Each complex has distinct and important roles in chromatin dynamics, gene expression and differentiation. In yeast and Drosophila, Smc6 is involved in recombinational repair, restarting collapsed replication forks and prevention of recombination in repetitive sequences such as rDNA and pericentromeric heterochromatin. Although such DNA damage control mechanisms, as well as highly dynamic changes in chromatin composition and function, are essential for gametogenesis, knowledge on Smc6 function in mammalian systems is limited. We therefore have investigated the role of Smc6 during mammalian spermatogonial differentiation, meiosis and subsequent spermiogenesis. We found that, during mouse spermatogenesis, Smc6 functions as part of meiotic pericentromeric heterochromatin domains that are initiated when differentiating spermatogonia become irreversibly committed toward meiosis. To our knowledge, we are the first to provide insight into how commitment toward meiosis alters chromatin structure and dynamics, thereby setting apart differentiating spermatogonia from the undifferentiated spermatogonia, including the spermatogonial stem cells. Interestingly, Smc6 is not essential for spermatogonial mitosis, whereas Smc6-negative meiotic cells appear unable to finish their first meiotic division. Importantly, during meiosis, we find that DNA repair or recombination sites, marked by γH2AX or Rad51 respectively, do not co-localize with the pericentromeric heterochromatin domains where Smc6 is located. Considering the repetitive nature of these domains and that Smc6 has been previously shown to prevent recombination in repetitive sequences, we hypothesize that Smc6 has a role in the prevention of aberrant recombination events between pericentromeric regions during the first meiotic prophase that would otherwise cause chromosomal aberrations leading to apoptosis, meiotic arrest or aneuploidies.
染色质的结构和功能在很大程度上取决于结构性维持染色体(SMC)蛋白家族的六个成员,它们形成三个异二聚体复合物:Smc1/3(黏合)、Smc2/4(凝聚)和 Smc5/6。每个复合物在染色质动力学、基因表达和分化中都具有独特而重要的作用。在酵母和果蝇中,Smc6 参与重组修复、重新启动崩溃的复制叉以及防止 rDNA 和着丝粒异染色质等重复序列中的重组。尽管这些 DNA 损伤控制机制以及染色质组成和功能的高度动态变化对于配子发生至关重要,但对哺乳动物系统中 Smc6 功能的了解是有限的。因此,我们研究了 Smc6 在哺乳动物精原细胞分化、减数分裂和随后的精子发生过程中的作用。我们发现,在小鼠精子发生过程中,Smc6 作为减数分裂着丝粒异染色质域的一部分发挥作用,这些域在分化的精原细胞不可逆地向减数分裂方向分化时开始形成。据我们所知,我们是第一个深入了解向减数分裂的定向如何改变染色质结构和动力学的,从而将分化的精原细胞与未分化的精原细胞(包括精原干细胞)区分开来。有趣的是,Smc6 对于精原细胞有丝分裂不是必需的,而 Smc6 阴性的减数分裂细胞似乎无法完成其第一次减数分裂。重要的是,在减数分裂过程中,我们发现 DNA 修复或重组位点,分别用 γH2AX 或 Rad51 标记,不与 Smc6 所在的着丝粒异染色质域共定位。考虑到这些域的重复性质,以及 Smc6 先前已被证明可防止重复序列中的重组,我们假设 Smc6 在防止第一次减数前期着丝粒区之间异常重组事件中发挥作用,否则这些事件会导致染色体异常,导致细胞凋亡、减数分裂停滞或非整倍体。