Mehta Gunjan D, Rizvi Syed Meraj Azhar, Ghosh Santanu Kumar
Department of Biosciences and Bioengineering, Wadhwani Research Centre for Biosciences and Bioengineering, Indian Institute of Technology, Bombay, India.
Biochim Biophys Acta. 2012 Aug;1823(8):1324-42. doi: 10.1016/j.bbamcr.2012.05.027. Epub 2012 Jun 5.
Ability to reproduce is one of the hallmark features of all life forms by which new organisms are produced from their progenitors. During this process each cell duplicates its genome and passes a copy of its genome to the daughter cells along with the cellular matrix. Unlike bacteria, in eukaryotes there is a definite time gap between when the genome is duplicated and when it is physically separated. Therefore, for precise halving of the duplicated genome into two, it is required that each pair of duplicated chromosomes, termed sister chromatids, should be paired together in a binary fashion from the moment they are generated. This pairing function between the duplicated genome is primarily provided by a multimeric protein complex, called cohesin. Thus, genome integrity largely depends on cohesin as it ensures faithful chromosome segregation by holding the sister chromatids glued together from S phase to anaphase. In this review, we have discussed the life cycle of cohesin during both mitotic and meiotic cell divisions including the structure and architecture of cohesin complex, relevance of cohesin associated proteins, mechanism of cohesin loading onto the chromatin, cohesion establishment and the mechanism of cohesin disassembly during anaphase to separate the sister chromatids. We have also focused on the role of posttranslational modifications in cohesin biology. For better understanding of the complexity of the cohesin regulatory network to the readers, we have presented an interactome profiling of cohesin core subunits in budding yeast during mitosis and meiosis.
繁殖能力是所有生命形式的标志性特征之一,通过这一特征新生物体由其祖先产生。在这个过程中,每个细胞复制其基因组,并将基因组的一份拷贝连同细胞基质传递给子细胞。与细菌不同,在真核生物中,基因组复制和物理分离之间存在明确的时间间隔。因此,为了将复制的基因组精确地减半为两份,要求每对复制的染色体(称为姐妹染色单体)从产生之时起就以二元方式配对在一起。复制基因组之间的这种配对功能主要由一种多聚体蛋白复合物——黏连蛋白提供。因此,基因组完整性在很大程度上依赖于黏连蛋白,因为它通过在从S期到后期将姐妹染色单体黏连在一起,确保了染色体的忠实分离。在这篇综述中,我们讨论了黏连蛋白在有丝分裂和减数分裂细胞分裂过程中的生命周期,包括黏连蛋白复合物的结构和架构、黏连蛋白相关蛋白的相关性、黏连蛋白加载到染色质上的机制、黏连的建立以及后期黏连蛋白解离以分离姐妹染色单体的机制。我们还重点关注了翻译后修饰在黏连蛋白生物学中的作用。为了让读者更好地理解黏连蛋白调控网络的复杂性,我们展示了芽殖酵母在有丝分裂和减数分裂过程中黏连蛋白核心亚基的相互作用组图谱。