Su Zhangli, Tian Mengxue, Shibata Etsuko, Shibata Yoshiyuki, Yang Tianyi, Wang Zhenjia, Jin Fulai, Zang Chongzhi, Dutta Anindya
bioRxiv. 2025 Apr 7:2024.12.18.629220. doi: 10.1101/2024.12.18.629220.
We report a multi-omics study in a human cell line with mutations in three subunits of Origin Recognition Complex (ORC). The ORC subunits bind to DNA independent of each other in addition to as part of a common six-subunit ORC. DNA-bound ORC2 compacts chromatin and attracts repressive histone marks to focal areas of the genome, but ORC2 also activates chromatin at many sites and protects the genes from repressive marks. The epigenetic changes regulate hundreds of genes, including some epigenetic regulators, adding an indirect mechanism by which ORC2 regulates epigenetics without local binding. DNA-bound ORC2 also prevents the acquisition of CTCF at focal sites in the genome to regulate chromatin loops and indirectly affect epigenetics. Thus, our study reveals the genes and ORC1 regions bound by individual ORC subunits and suggests their role as epigenetics and chromosome structure regulators, independent of the role of the six-subunit ORC in DNA replication.
我们报告了一项在具有起源识别复合物(ORC)三个亚基突变的人类细胞系中的多组学研究。除了作为常见的六亚基ORC的一部分外,ORC亚基彼此独立地与DNA结合。与DNA结合的ORC2使染色质压缩,并将抑制性组蛋白标记吸引到基因组的焦点区域,但ORC2也在许多位点激活染色质,并保护基因免受抑制性标记的影响。表观遗传变化调节数百个基因,包括一些表观遗传调节因子,增加了一种间接机制,通过该机制ORC2无需局部结合即可调节表观遗传学。与DNA结合的ORC2还可防止在基因组焦点位点获得CTCF,以调节染色质环并间接影响表观遗传学。因此,我们的研究揭示了单个ORC亚基结合的基因和ORC1区域,并表明它们作为表观遗传学和染色体结构调节因子的作用,独立于六亚基ORC在DNA复制中的作用。