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人类起源识别复合体的结构

Architecture of the human origin recognition complex.

作者信息

Dhar S K, Delmolino L, Dutta A

机构信息

Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

J Biol Chem. 2001 Aug 3;276(31):29067-71. doi: 10.1074/jbc.M103078200. Epub 2001 Jun 6.

Abstract

All the human homologs of the six subunits of Saccharomyces cerevisiae origin recognition complex have been reported so far. However, not much has been reported on the nature and the characteristics of the human origin recognition complex. In an attempt to purify recombinant human ORC from insect cells infected with baculoviruses expressing HsORC subunits, we found that human ORC2, -3, -4, and -5 form a core complex. HsORC1 and HsORC6 subunits did not enter into this core complex, suggesting that the interaction of these two subunits with the core ORC2-5 complex is extremely labile. We found that the C-terminal region of ORC2 interacts directly with the N-terminal region of ORC3. The C-terminal region of ORC3 was, however, necessary to bring ORC4 and ORC5 into the core complex. A fragment containing the N-terminal 200 residues of ORC3 (ORC3N) competitively inhibited the ORC2-ORC3 interaction. Overexpression of this fragment in U2OS cells blocked the cells in G(1), providing the first evidence that a mammalian ORC subunit is important for the G(1)-S transition in mammalian cells.

摘要

到目前为止,已报道了酿酒酵母起始识别复合物六个亚基的所有人类同源物。然而,关于人类起始识别复合物的性质和特征,报道并不多。为了从感染了表达人源起始识别复合物(HsORC)亚基的杆状病毒的昆虫细胞中纯化重组人源起始识别复合物,我们发现人源ORC2、-3、-4和-5形成了一个核心复合物。HsORC1和HsORC6亚基没有进入这个核心复合物,这表明这两个亚基与核心ORC2-5复合物的相互作用极其不稳定。我们发现ORC2的C末端区域直接与ORC3的N末端区域相互作用。然而,ORC3的C末端区域是将ORC4和ORC5纳入核心复合物所必需的。包含ORC3 N末端200个残基的片段(ORC3N)竞争性抑制ORC2-ORC3相互作用。在U2OS细胞中过表达该片段会使细胞停滞在G1期,这首次证明了哺乳动物起始识别复合物亚基对哺乳动物细胞从G1期到S期的转变很重要。

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