Skip Navigation



Journal of Biochemistry Advance Access published online on January 22, 2008

Journal of Biochemistry, doi:10.1093/jb/mvn005
This Article
Right arrow Advance Access manuscript (PDF)
Right arrow All Versions of this Article:
143/4/455    most recent
mvn005v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Request Permissions
Google Scholar
Right arrow Articles by Makise, M.
Right arrow Articles by Mizushima, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Makise, M.
Right arrow Articles by Mizushima, T.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2008 The Japanese Biochemical Society

Analysis of Origin Recognition Complex In Saccharomyces Cerevisiae, By Use of Degron Mutants

Masaki Makise1,3, Nanako Matsui1,3, Fumiko Yamairi1,3, Naoko Takahashi2, Masaya Takehara1, Teita Asano1 and Tohru Mizushima1,#

1Graduate School of Medical and Pharmaceutical Sciences, Kumamoto University, Kumamoto 862-0973, Japan.
2Faculty of Pharmaceutical Sciences, Okayama University, Okayama 700-8530, Japan.
3These three authors equally contribute to this work.

#To whom correspondence should be addressed: Prof. Mizushima, Tohru: Graduate School of Medical and Pharmaceutical Sciences, Kumamoto University, Kumamoto 862-0973, Japan. Tel: +81-96-371-4323, Fax: +81-96-371-4323, E-mail: mizu{at}gpo.kumamoto-u.ac.jp

Received November 22, 2007; Accepted December 7, 2007


   Abstract

Origin recognition complex (ORC), a six-protein complex (Orc1p-Orc6p), may deeply involved in initiation of chromosomal DNA replication. However, since most temperature-sensitive orc mutants of Saccharomyces cerevisiae show the accumulation of cells with nearly 2C DNA content, the exact stage at which ORC acts is not fully understood. In this study, we constructed a heat inducible degron mutant for each ORC subunit. As well as each targeted subunit, other subunits of ORC were also rapidly degraded under non-permissive conditions. In the orc5 degron mutant, incubation under the non-permissive conditions caused accumulation of cells with nearly 2C DNA content, and phosphorylation of Rad53p. When Orc5p (ORC) is depleted, this inhibits G1/S transition and formation of a pre-replicative complex (pre-RC). For pre-RC to form, and G1/S transition to proceed, Orc5p (ORC) must be present in late G1, rather than early G1, or G2/M. Block and release experiments revealed that Orc5p (ORC) is not necessary for S and G2/M phase progression. We therefore propose that ORC is necessary for the G1/S transition and pre-RC formation, and accumulation of cells with nearly 2C DNA content seen in various orc mutants is due to inefficient pre-RC formation, and/or induction of checkpoint systems.

Key Words: DNA replication, heat inducible degron mutant, ORC, Orc5p, pre-replicative complex


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.