Wallace Heather A, Klebba Joseph E, Kusch Thomas, Rogers Gregory C, Bosco Giovanni
Department of Genetics, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire 03755.
Department of Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, Arizona 85721.
G3 (Bethesda). 2015 Mar 9;5(5):803-17. doi: 10.1534/g3.115.016634.
The spatial organization of the genome within the eukaryotic nucleus is a dynamic process that plays a central role in cellular processes such as gene expression, DNA replication, and chromosome segregation. Condensins are conserved multi-subunit protein complexes that contribute to chromosome organization by regulating chromosome compaction and homolog pairing. Previous work in our laboratory has shown that the Cap-H2 subunit of condensin II physically and genetically interacts with the Drosophila homolog of human MORF4-related gene on chromosome 15 (MRG15). Like Cap-H2, Mrg15 is required for interphase chromosome compaction and homolog pairing. However, the mechanism by which Mrg15 and Cap-H2 cooperate to maintain interphase chromatin organization remains unclear. Here, we show that Cap-H2 localizes to interband regions on polytene chromosomes and co-localizes with Mrg15 at regions of active transcription across the genome. We show that co-localization of Cap-H2 on polytene chromosomes is partially dependent on Mrg15. We have identified a binding motif within Cap-H2 that is essential for its interaction with Mrg15, and have found that mutation of this motif results in loss of localization of Cap-H2 on polytene chromosomes and results in partial suppression of Cap-H2-mediated compaction and homolog unpairing. Our data are consistent with a model in which Mrg15 acts as a loading factor to facilitate Cap-H2 binding to chromatin and mediate changes in chromatin organization.
真核细胞核内基因组的空间组织是一个动态过程,在基因表达、DNA复制和染色体分离等细胞过程中起着核心作用。凝聚素是保守的多亚基蛋白复合物,通过调节染色体压缩和同源配对来促进染色体组织。我们实验室之前的工作表明,凝聚素II的Cap-H2亚基在物理和遗传上与位于15号染色体上的人类MORF4相关基因(MRG15)的果蝇同源物相互作用。与Cap-H2一样,Mrg15也是间期染色体压缩和同源配对所必需的。然而,Mrg15和Cap-H2协同维持间期染色质组织的机制仍不清楚。在这里,我们表明Cap-H2定位于多线染色体的间带区域,并在全基因组的活跃转录区域与Mrg15共定位。我们表明,Cap-H2在多线染色体上的共定位部分依赖于Mrg15。我们在Cap-H2中鉴定出一个对其与Mrg15相互作用至关重要的结合基序,并发现该基序的突变导致Cap-H2在多线染色体上的定位丧失,并导致Cap-H2介导的压缩和同源解配对的部分抑制。我们的数据与一个模型一致,即Mrg15作为一个装载因子,促进Cap-H2与染色质结合并介导染色质组织的变化。