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

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NATURE REVIEWS MOLECULAR CELL BIOLOGY
卷 14, 期 9, 页码 563-580

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NATURE PUBLISHING GROUP
DOI: 10.1038/nrm3640

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资金

  1. US National Institutes of Health [GM68762, CA112967, ES015339, ES020466]
  2. Volkswagenstiftung (Lichtenberg Program)
  3. Deutsche Forschungsgemeinschaft [KFO-286, SFB-832, SFB-829, RE2246/2-1]
  4. Helmholtz-Gemeinschaft (Preclinical Comprehensive Cancer Center)
  5. Deutsche Jose Carreras Stiftung [DJCLS-R12/26]
  6. David H. Koch Fund

向作者/读者索取更多资源

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 beta TrCP), 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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