Merigliano Chiara, Ryu Taehyun, See Colby D, Caridi Christopher P, Li Xiao, Butova Nadejda L, Reynolds Trevor W, Deng Changfeng, Chenoweth David M, Capelson Maya, Chiolo Irene
University of Southern California, Molecular and Computational Biology Department, Los Angeles, CA, USA.
Harvard Medical School, Department of Genetics, Boston, MA, USA.
bioRxiv. 2024 Jul 18:2023.12.07.570729. doi: 10.1101/2023.12.07.570729.
Phase separation forms membraneless compartments in the nuclei, including by establishing heterochromatin "domains" and repair foci. Pericentromeric heterochromatin mostly comprises repeated sequences prone to aberrant recombination, and "safe" homologous recombination (HR) repair of these sequences requires the movement of repair sites to the nuclear periphery before Rad51 recruitment and strand invasion. How this mobilization initiates is unknown, and the contribution of phase separation to these dynamics is unclear. Here, we show that Nup98 nucleoporin is recruited to heterochromatic repair sites before relocalization through Sec13 or Nup88 nucleoporins, and downstream from the Smc5/6 complex and SUMOylation. Remarkably, the phase separation properties of Nup98 are required and sufficient to mobilize repair sites and exclude Rad51, thus preventing aberrant recombination while promoting HR repair. Disrupting this pathway results in heterochromatin repair defects and widespread chromosome rearrangements, revealing a novel "off-pore" role for nucleoporins and phase separation in nuclear dynamics and genome integrity in a multicellular eukaryote.
相分离在细胞核中形成无膜区室,包括通过建立异染色质“结构域”和修复位点来实现。着丝粒周围异染色质大多由易于发生异常重组的重复序列组成,而这些序列的“安全”同源重组(HR)修复需要在Rad51募集和链侵入之前将修复位点转移到核周。这种动员如何启动尚不清楚,相分离对这些动态过程的贡献也不明确。在这里,我们表明核孔蛋白Nup98在通过Sec13或Nup88核孔蛋白重新定位之前被募集到异染色质修复位点,且在Smc5/6复合体和SUMO化作用的下游。值得注意的是,Nup98的相分离特性对于动员修复位点和排除Rad51是必需且足够的,从而在促进HR修复的同时防止异常重组。破坏这一途径会导致异染色质修复缺陷和广泛的染色体重排,揭示了核孔蛋白和相分离在多细胞真核生物的核动态和基因组完整性中的一种新的“孔外”作用。