Literature DB >> 11395502

Architecture of the human origin recognition complex.

S K Dhar1, L Delmolino, A Dutta.   

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.

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Year:  2001        PMID: 11395502     DOI: 10.1074/jbc.M103078200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  53 in total

1.  Cell cycle-dependent regulation of the association between origin recognition proteins and somatic cell chromatin.

Authors:  Wei-Hsin Sun; Thomas R Coleman; Melvin L DePamphilis
Journal:  EMBO J       Date:  2002-03-15       Impact factor: 11.598

2.  The latency-associated nuclear antigen of Kaposi's sarcoma-associated herpesvirus supports latent DNA replication in dividing cells.

Authors:  Jianhong Hu; Alexander C Garber; Rolf Renne
Journal:  J Virol       Date:  2002-11       Impact factor: 5.103

3.  Functional domains involved in the interaction between Orc1 and transcriptional repressor AlF-C that bind to an origin/promoter of the rat aldolase B gene.

Authors:  Yasushi Saitoh; Satoru Miyagi; Hiroyoshi Ariga; Ken-ichi Tsutsumi
Journal:  Nucleic Acids Res       Date:  2002-12-01       Impact factor: 16.971

4.  Sequence-independent DNA binding and replication initiation by the human origin recognition complex.

Authors:  Sanjay Vashee; Christin Cvetic; Wenyan Lu; Pamela Simancek; Thomas J Kelly; Johannes C Walter
Journal:  Genes Dev       Date:  2003-08-01       Impact factor: 11.361

5.  Dynamic association of ORCA with prereplicative complex components regulates DNA replication initiation.

Authors:  Zhen Shen; Arindam Chakraborty; Ankur Jain; Sumanprava Giri; Taekjip Ha; Kannanganattu V Prasanth; Supriya G Prasanth
Journal:  Mol Cell Biol       Date:  2012-05-29       Impact factor: 4.272

6.  Binding of AlF-C, an Orc1-binding transcriptional regulator, enhances replicator activity of the rat aldolase B origin.

Authors:  Hiroyuki Minami; Junko Takahashi; Asami Suto; Yasushi Saitoh; Ken-ichi Tsutsumi
Journal:  Mol Cell Biol       Date:  2006-09-18       Impact factor: 4.272

7.  Studies of the properties of human origin recognition complex and its Walker A motif mutants.

Authors:  Jennifer Giordano-Coltart; Carol Y Ying; Jean Gautier; Jerard Hurwitz
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-23       Impact factor: 11.205

8.  Recruitment of ORC or CDC6 to DNA is sufficient to create an artificial origin of replication in mammalian cells.

Authors:  David Y Takeda; Yoshiyuki Shibata; Jeffrey D Parvin; Anindya Dutta
Journal:  Genes Dev       Date:  2005-12-01       Impact factor: 11.361

9.  A structural role for ATP in the formation and stability of the human origin recognition complex.

Authors:  Anand Ranjan; Manfred Gossen
Journal:  Proc Natl Acad Sci U S A       Date:  2006-03-20       Impact factor: 11.205

10.  Ubiquitylation, phosphorylation and Orc2 modulate the subcellular location of Orc1 and prevent it from inducing apoptosis.

Authors:  Tapas Saha; Soma Ghosh; Alex Vassilev; Melvin L DePamphilis
Journal:  J Cell Sci       Date:  2006-03-14       Impact factor: 5.285

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