Genome stability versus transcript diversity

DNA Repair (Amst). 2016 Aug:44:81-86. doi: 10.1016/j.dnarep.2016.05.010. Epub 2016 May 16.

Abstract

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.

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

Publication types

  • Review
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing
  • DNA Damage
  • DNA Repair*
  • DNA Replication
  • Gene Expression Profiling
  • Genetic Variation*
  • Genome, Human
  • Genomic Instability*
  • Humans
  • Protein Biosynthesis
  • Proteome
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Transcriptome*

Substances

  • Proteome
  • RNA, Messenger