[The post-transcriptional regulation of the DNA damage response]

Deling Lin1, Ying Luo2, Yi Song3

  • 1Medical Faculty of Kunming University of Science and Technology, Kunming 650500, China; Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China.

Insights

The DNA damage response (DDR) involves microRNAs and RNA-binding proteins (RBPs) in regulating cellular repair mechanisms. This review highlights their crucial roles in post-transcriptional control of the DDR pathway.

Area of Science:

  • Molecular Biology
  • Cell Biology
  • Genetics

Context:

  • The DNA damage response (DDR) is a critical cellular network activated by DNA damage to halt cell division and initiate repair.
  • Research traditionally focused on transcriptional and protein modification aspects of DDR.
  • Recent attention has shifted towards the roles of mRNA stability and translation in DDR.

Purpose:

  • To review recent findings on the post-transcriptional regulation of the DNA damage response (DDR).
  • To highlight the involvement of microRNAs and RNA-binding proteins (RBPs) in DDR.
  • To discuss how these molecules contribute to genome protection.

Summary:

  • MicroRNAs and RBPs are increasingly recognized for their roles in the DDR.
  • These molecules regulate DDR through post-transcriptional mechanisms, affecting mRNA stability and translation.
  • Their collective action is vital for maintaining genomic integrity following DNA damage.

Impact:

  • Advances understanding of DDR regulation beyond transcriptional control.
  • Identifies novel targets for therapeutic interventions in diseases involving DNA damage.
  • Provides insights into the complex interplay of RNA molecules in cellular stress responses.

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