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Genome stability versus transcript diversity

期刊

DNA REPAIR
卷 44, 期 -, 页码 81-86

出版社

ELSEVIER
DOI: 10.1016/j.dnarep.2016.05.010

关键词

RNA splicing; RNA transcription; Protein translation; Post-transcriptional RNA processing; DNA damage response; DNA repair; Polymerase fidelity; Proteomic diversity

资金

  1. National Institute of Environmental Health Sciences [1R21ES020946]
  2. National Human Genome Research Institute [1R01HG006786]
  3. University of Michigan Pancreatic Cancer Center
  4. University of Michigan School of Public Health Environmental Toxicology and Epidemiology Program, National Institute of Environmental Health Sciences [T32ES007062]

向作者/读者索取更多资源

Our genome is protected from the introduction of mutations by high fidelity replication and an extensive network of DNA damage response and repair mechanisms. However, the expression of our genome, via RNA and protein synthesis, allows for more diversity in translating genetic information. In addition, the splicing process has become less stringent over evolutionary time allowing for a substantial increase in the diversity of transcripts generated. The result is a diverse transcriptome and proteome that harbor selective advantages over a more tightly regulated system. Here, we describe mechanisms in place that both safeguard the genome and promote translational diversity, with emphasis on post-transcriptional RNA processing. (C) 2016 Elsevier B.V. All rights reserved.

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