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Treacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA damage response.

Proceedings of the National Academy of Sciences of the United States of America | 2014

The signal transduction pathway of the DNA damage response (DDR) is activated to maintain genomic integrity following DNA damage. The DDR promotes genomic integrity by regulating a large network of cellular activities that range from DNA replication and repair to transcription, RNA splicing, and metabolism. In this study we define an interaction between the DDR factor NBS1 and TCOF1, a nucleolar protein that regulates ribosomal DNA (rDNA) transcription and is mutated in Treacher Collins syndrome. We show that NBS1 relocalizes to nucleoli after DNA damage in a manner dependent on TCOF1 and on casein kinase II and ATM, which are known to modify TCOF1 by phosphorylation. Moreover, we identify a putative ATM phosphorylation site that is required for NBS1 relocalization to nucleoli in response to DNA damage. Last, we report that TCOF1 promotes cellular resistance to DNA damaging agents. Collectively, our findings identify TCOF1 as a DDR factor that could cooperate with ATM and NBS1 to suppress inappropriate rDNA transcription and maintain genomic integrity after DNA damage.

Pubmed ID: 25512513 RIS Download

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Associated grants

  • Agency: NIGMS NIH HHS, United States
    Id: GM44664
  • Agency: NIA NIH HHS, United States
    Id: AG011085
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM044664
  • Agency: NIA NIH HHS, United States
    Id: R01 AG011085
  • Agency: Howard Hughes Medical Institute, United States
  • Agency: NIGMS NIH HHS, United States
    Id: R37 GM044664

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