Literature DB >> 17167417

Phosphorylation of Sld2 and Sld3 by cyclin-dependent kinases promotes DNA replication in budding yeast.

Philip Zegerman1, John F X Diffley.   

Abstract

Cyclin-dependent kinases (CDKs) drive major cell cycle events including the initiation of chromosomal DNA replication. We identified two S phase CDK (S-CDK) phosphorylation sites in the budding yeast Sld3 protein that, together, are essential for DNA replication. Here we show that, when phosphorylated, these sites bind to the amino-terminal BRCT repeats of Dpb11. An Sld3-Dpb11 fusion construct bypasses the requirement for both Sld3 phosphorylation and the N-terminal BRCT repeats of Dpb11. Co-expression of this fusion with a phospho-mimicking mutant in a second essential CDK substrate, Sld2, promotes DNA replication in the absence of S-CDK. Therefore, Sld2 and Sld3 are the minimal set of S-CDK targets required for DNA replication. DNA replication in cells lacking G1 phase CDK (G1-CDK) required expression of the Cdc7 kinase regulatory subunit, Dbf4, as well as Sld2 and Sld3 bypass. Our results help to explain how G1- and S-CDKs promote DNA replication in yeast.

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Year:  2006        PMID: 17167417     DOI: 10.1038/nature05432

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  263 in total

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Review 8.  Regulation of DNA replication by chromatin structures: accessibility and recruitment.

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9.  Rad53 downregulates mitotic gene transcription by inhibiting the transcriptional activator Ndd1.

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10.  Cdc45 protein-single-stranded DNA interaction is important for stalling the helicase during replication stress.

Authors:  Irina Bruck; Daniel L Kaplan
Journal:  J Biol Chem       Date:  2013-02-04       Impact factor: 5.157

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