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Shaping mitotic chromosomes: From classical concepts to molecular mechanisms

期刊

BIOESSAYS
卷 37, 期 7, 页码 755-766

出版社

WILEY
DOI: 10.1002/bies.201500020

关键词

chromosome condensation; chromosome segregation; cohesin; condensin; mitosis; SMC complex; topoisomerase II

资金

  1. EMBL
  2. German Research Foundation [HA5853/1-2, HA5853/2-1]

向作者/读者索取更多资源

How eukaryotic genomes are packaged into compact cylindrical chromosomes in preparation for cell divisions has remained one of the major unsolved questions of cell biology. Novel approaches to study the topology of DNA helices inside the nuclei of intact cells, paired with computational modeling and precise biomechanical measurements of isolated chromosomes, have advanced our understanding of mitotic chromosome architecture. In this Review Essay, we discuss - in light of these recent insights - the role of chromatin architecture and the functions and possible mechanisms of SMC protein complexes and other molecular machines in the formation of mitotic chromosomes. Based on the information available, we propose a stepwise model of mitotic chromosome condensation that envisions the sequential generation of intra-chromosomal linkages by condensin complexes in the context of cohesin-mediated inter-chromosomal linkages, assisted by topoisomerase II. The described scenario results in rod-shaped metaphase chromosomes ready for their segregation to the cell poles.

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