Literature DB >> 2279699

Subcellular localization of yeast CDC46 varies with the cell cycle.

K M Hennessy1, C D Clark, D Botstein.   

Abstract

The Saccharomyces cerevisiae CDC46 protein accumulates in the nucleus of nondividing interphase cells. Soon after the cell has become committed to division, there is a rapid disappearance of CDC46 protein from the nucleus. This shift is not a consequence of variation in total CDC46 protein levels and is associated with DNA replication at the G1-S boundary. We propose that the CDC46 protein, which is required for DNA replication, becomes mobilized quickly from the cytoplasm into the nucleus as mitosis is completed and persists there until the next round of division is initiated. This partitioning of proteins in a cell cycle-dependent manner illustrates a general means of regulating events that must occur only once in each cycle, such as DNA initiation.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2279699     DOI: 10.1101/gad.4.12b.2252

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  77 in total

1.  Dbf4p, an essential S phase-promoting factor, is targeted for degradation by the anaphase-promoting complex.

Authors:  M F Ferreira; C Santocanale; L S Drury; J F Diffley
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

2.  Cell cycle control of Cdc7p kinase activity through regulation of Dbf4p stability.

Authors:  G Oshiro; J C Owens; Y Shellman; R A Sclafani; J J Li
Journal:  Mol Cell Biol       Date:  1999-07       Impact factor: 4.272

3.  MCM2-7 proteins are essential components of prereplicative complexes that accumulate cooperatively in the nucleus during G1-phase and are required to establish, but not maintain, the S-phase checkpoint.

Authors:  K Labib; S E Kearsey; J F Diffley
Journal:  Mol Biol Cell       Date:  2001-11       Impact factor: 4.138

4.  The role of nucleotide binding and hydrolysis in the function of the fission yeast cdc18(+) gene product.

Authors:  D DeRyckere; C L Smith; G S Martin
Journal:  Genetics       Date:  1999-04       Impact factor: 4.562

5.  At least three distinct proteins are necessary for the reconstitution of a specific multiprotein complex at a eukaryotic chromosomal origin of replication.

Authors:  H G Estes; B S Robinson; S Eisenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-01       Impact factor: 11.205

6.  Two bipartite NLSs mediate constitutive nuclear localization of Mcm10.

Authors:  Rebekah Burich; Ming Lei
Journal:  Curr Genet       Date:  2003-09-10       Impact factor: 3.886

Review 7.  Eukaryotic MCM proteins: beyond replication initiation.

Authors:  Susan L Forsburg
Journal:  Microbiol Mol Biol Rev       Date:  2004-03       Impact factor: 11.056

8.  Association of RPA with chromosomal replication origins requires an Mcm protein, and is regulated by Rad53, and cyclin- and Dbf4-dependent kinases.

Authors:  T Tanaka; K Nasmyth
Journal:  EMBO J       Date:  1998-09-01       Impact factor: 11.598

9.  Cell cycle-regulated nuclear import and export of Cdc47, a protein essential for initiation of DNA replication in budding yeast.

Authors:  S Dalton; L Whitbread
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-28       Impact factor: 11.205

10.  XMCM7, a novel member of the Xenopus MCM family, interacts with XMCM3 and colocalizes with it throughout replication.

Authors:  P Romanowski; M A Madine; R A Laskey
Journal:  Proc Natl Acad Sci U S A       Date:  1996-09-17       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.