Literature DB >> 23969844

Phospho-Ser/Thr-binding domains: navigating the cell cycle and DNA damage response.

H Christian Reinhardt1, Michael B Yaffe.   

Abstract

Coordinated progression through the cell cycle is a complex challenge for eukaryotic cells. Following genotoxic stress, diverse molecular signals must be integrated to establish checkpoints specific for each cell cycle stage, allowing time for various types of DNA repair. Phospho-Ser/Thr-binding domains have emerged as crucial regulators of cell cycle progression and DNA damage signalling. Such domains include 14-3-3 proteins, WW domains, Polo-box domains (in PLK1), WD40 repeats (including those in the E3 ligase SCF(βTrCP)), BRCT domains (including those in BRCA1) and FHA domains (such as in CHK2 and MDC1). Progress has been made in our understanding of the motif (or motifs) that these phospho-Ser/Thr-binding domains connect with on their targets and how these interactions influence the cell cycle and DNA damage response.

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Year:  2013        PMID: 23969844     DOI: 10.1038/nrm3640

Source DB:  PubMed          Journal:  Nat Rev Mol Cell Biol        ISSN: 1471-0072            Impact factor:   94.444


  238 in total

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Review 4.  Polo-like kinases: conservation and divergence in their functions and regulation.

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Journal:  Nat Rev Mol Cell Biol       Date:  2009-04       Impact factor: 94.444

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Journal:  Trends Biochem Sci       Date:  1995-09       Impact factor: 13.807

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Journal:  Cell       Date:  1996-03-22       Impact factor: 41.582

7.  Polo-like kinase-1 is a target of the DNA damage checkpoint.

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Journal:  Nat Cell Biol       Date:  2000-09       Impact factor: 28.824

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Journal:  Genes Cells       Date:  2000-06       Impact factor: 1.891

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10.  Phosphorylation of mitotic kinesin-like protein 2 by polo-like kinase 1 is required for cytokinesis.

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Journal:  J Cell Biol       Date:  2003-08-25       Impact factor: 10.539

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Review 5.  Structural insights into NHEJ: building up an integrated picture of the dynamic DSB repair super complex, one component and interaction at a time.

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Review 6.  Cell Cycle Regulation and Melanoma.

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Review 7.  Crosstalk between ubiquitin and other post-translational modifications on chromatin during double-strand break repair.

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8.  Ca2+-Stimulated AMPK-Dependent Phosphorylation of Exo1 Protects Stressed Replication Forks from Aberrant Resection.

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