From the Department of Chemical and Biological Sciences, Faculty of Science, Japan Women's University, Tokyo 112-8681, Japan.
the Graduate School of Humanities and Sciences, Ochanomizu University, Tokyo 112-8610, Japan.
J Biol Chem. 2013 Oct 18;288(42):30161-30171. doi: 10.1074/jbc.M113.492504. Epub 2013 Sep 3.
Origin recognition complex (ORC), consisting of six subunits ORC1-6, is known to bind to replication origins and function in the initiation of DNA replication in eukaryotic cells. In contrast to the fact that Saccharomyces cerevisiae ORC recognizes the replication origin in a sequence-specific manner, metazoan ORC has not exhibited strict sequence-specificity for DNA binding. Here we report that human ORC binds preferentially to G-quadruplex (G4)-preferable G-rich RNA or single-stranded DNA (ssDNA). We mapped the G-rich RNA-binding domain in the ORC1 subunit, in a region adjacent to its ATPase domain. This domain itself has an ability to preferentially recognize G4-preferable sequences of ssDNA. Furthermore, we found, by structure modeling, that the G-rich RNA-binding domain is similar to the N-terminal portion of AdoMet_MTase domain of mammalian DNA methyltransferase 1. Therefore, in contrast with the binding to double-stranded DNA, human ORC has an apparent sequence preference with respect to its RNA/ssDNA binding. Interestingly, this specificity coincides with the common signature present in most of the human replication origins. We expect that our findings provide new insights into the regulations of function and chromatin binding of metazoan ORCs.
起始识别复合物(ORC)由六个亚基 ORC1-6 组成,已知其与复制起始点结合,并在真核细胞中启动 DNA 复制。与酿酒酵母 ORC 以序列特异性方式识别复制起始点的事实相反,真核生物 ORC 对 DNA 结合没有表现出严格的序列特异性。在这里,我们报告人类 ORC 优先结合 G-四联体(G4)偏好性 G 丰富 RNA 或单链 DNA(ssDNA)。我们在 ORC1 亚基中定位了 G 丰富 RNA 结合域,该域位于其 ATP 酶结构域附近。该结构域本身具有优先识别 G4 偏好性 ssDNA 序列的能力。此外,我们通过结构建模发现,G 丰富 RNA 结合域与哺乳动物 DNA 甲基转移酶 1 的 AdoMet_MTase 结构域的 N 端部分相似。因此,与结合双链 DNA 相比,人类 ORC 对其 RNA/ssDNA 结合具有明显的序列偏好性。有趣的是,这种特异性与大多数人类复制起始点存在的共同特征一致。我们预计我们的发现将为真核生物 ORC 的功能调控和染色质结合提供新的见解。