Maresca Thomas J, Heald Rebecca
Department of Molecular and Cell Biology, University of California, Berkeley 94720-3200, USA.
Cell Cycle. 2006 Mar;5(6):589-91. doi: 10.4161/cc.5.6.2581. Epub 2006 Mar 15.
Faithful distribution of the genome to daughter cells requires that replicated chromatids are compacted and resolved from one another, and that functional kinetochores assemble at their centromeres to mediate spindle interactions. A molecular and mechanistic understanding of these critical processes is far from complete. We discovered that linker histone H1, a major chromatin component, is required for longitudinal compaction of replicated sperm chromosome arms in Xenopus laevis egg extracts that recapitulate the cell cycle in vitro. Due to their elongated structure, H1-depleted chromosomes could not be aligned or segregated by the spindle despite apparently normal kinetochore assembly. Interestingly, enrichment of H1 onto chromatin required passage through interphase, when DNA replication takes place. Here we show that interphase-dependent loading is also a feature of kinetochore components including Ndc80. Thus, linker histone H1 contributes to chromosome condensation in vertebrates, and important molecular determinants of mitotic chromosome and kinetochore structure and function are established during interphase.
基因组向子细胞的忠实分配要求复制后的染色单体相互压缩并分离,且功能性动粒在其着丝粒处组装以介导纺锤体相互作用。对这些关键过程的分子和机制理解远未完成。我们发现,连接组蛋白H1是染色质的主要成分,在非洲爪蟾卵提取物中,它是体外重现细胞周期时复制精子染色体臂纵向压缩所必需的。由于其细长的结构,尽管动粒组装明显正常,但H1缺失的染色体无法被纺锤体排列或分离。有趣的是,H1在染色质上的富集需要经过DNA复制发生的间期。在这里我们表明,依赖间期的加载也是包括Ndc80在内的动粒成分的一个特征。因此,连接组蛋白H1有助于脊椎动物染色体的浓缩,且有丝分裂染色体以及动粒结构和功能的重要分子决定因素是在间期建立的。