Literature DB >> 11805087

The human cruciform-binding protein, CBP, is involved in DNA replication and associates in vivo with mammalian replication origins.

Olivia Novac1, David Alvarez, Christopher E Pearson, Gerald B Price, Maria Zannis-Hadjopoulos.   

Abstract

We previously identified and purified from human (HeLa) cells a 66-kDa cruciform-binding protein, CBP, with binding specificity for cruciform DNA regardless of its sequence. DNA cruciforms have been implicated in the regulation of initiation of DNA replication. CBP is a member of the 14-3-3 family of proteins, which are conserved regulatory molecules expressed in all eukaryotes. Here, the in vivo association of CBP/14-3-3 with mammalian origins of DNA replication was analyzed by studying its association with the monkey replication origins ors8 and ors12, as assayed by a chromatin immunoprecipitation assay and quantitative PCR analysis. The association of the 14-3-3beta, -epsilon, -gamma, and -zeta isoforms with these origins was found to be approximately 9-fold higher, compared with other portions of the genome, in logarithmically growing cells. In addition, the association of these isoforms with ors8 and ors12 was also analyzed as a function of the cell cycle. Higher binding of 14-3-3beta, -epsilon, -gamma, and -zeta isoforms with ors8 and ors12 was found at the G(1)/S border, by comparison with other stages of the cell cycle. The CBP/14-3-3 cruciform binding activity was also found to be maximal at the G(1)/S boundary. The involvement of 14-3-3 in mammalian DNA replication was analyzed by studying the effect of anti-14-3-3beta, -epsilon, -gamma, and -zeta antibodies in the in vitro replication of p186, a plasmid containing the minimal replication origin of ors8. Anti-14-3-3epsilon, -gamma, and -zeta antibodies alone or in combination inhibited p186 replication by approximately 50-80%, while anti-14-3-3beta antibodies had a lesser effect ( approximately 25-50%). All of the antibodies tested were also able to interfere with CBP binding to cruciform DNA. The results indicate that CBP/14-3-3 is an origin-binding protein, acting at the initiation step of DNA replication by binding to cruciform-containing molecules, and dissociates after origin firing.

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Year:  2002        PMID: 11805087     DOI: 10.1074/jbc.M107902200

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


  8 in total

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Authors:  Laurent Miccoli; Isabelle Frouin; Olivia Novac; Domenic Di Paola; Francis Harper; Maria Zannis-Hadjopoulos; Giovanni Maga; Denis S F Biard; Jaime F Angulo
Journal:  Mol Cell Biol       Date:  2005-05       Impact factor: 4.272

2.  14-3-3 checkpoint regulatory proteins interact specifically with DNA repair protein human exonuclease 1 (hEXO1) via a semi-conserved motif.

Authors:  Sofie Dabros Andersen; Guido Keijzers; Emmanouil Rampakakis; Kim Engels; Patricia Luhn; Mahmoud El-Shemerly; Finn Cilius Nielsen; Yuhong Du; Alfred May; Vilhelm A Bohr; Stefano Ferrari; Maria Zannis-Hadjopoulos; Haian Fu; Lene Juel Rasmussen
Journal:  DNA Repair (Amst)       Date:  2012-01-04

3.  Transient dsDNA breaks during pre-replication complex assembly.

Authors:  Emmanouil Rampakakis; Maria Zannis-Hadjopoulos
Journal:  Nucleic Acids Res       Date:  2009-07-28       Impact factor: 16.971

4.  Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.

Authors:  Hiroki Kurahashi; Hidehito Inagaki; Kouji Yamada; Tamae Ohye; Mariko Taniguchi; Beverly S Emanuel; Tatsushi Toda
Journal:  J Biol Chem       Date:  2004-06-20       Impact factor: 5.157

5.  The distribution of inverted repeat sequences in the Saccharomyces cerevisiae genome.

Authors:  Eva M Strawbridge; Gary Benson; Yevgeniy Gelfand; Craig J Benham
Journal:  Curr Genet       Date:  2010-05-06       Impact factor: 3.886

6.  Deletion of the cruciform binding domain in CBP/14-3-3 displays reduced origin binding and initiation of DNA replication in budding yeast.

Authors:  Wafaa Yahyaoui; Mario Callejo; Gerald B Price; Maria Zannis-Hadjopoulos
Journal:  BMC Mol Biol       Date:  2007-04-12       Impact factor: 2.946

7.  Amplification of a transgene within a long array of replication origins favors higher gene expression in animal cells.

Authors:  Kiwamu Ohsaki; Yusuke Ohgaki; Noriaki Shimizu
Journal:  PLoS One       Date:  2017-04-12       Impact factor: 3.240

8.  Emerging players in the initiation of eukaryotic DNA replication.

Authors:  Zhen Shen; Supriya G Prasanth
Journal:  Cell Div       Date:  2012-10-17       Impact factor: 5.130

  8 in total

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