p53 and its isoforms in DNA double-stranded break repair

Yu-Xi Zhang1, Wen-Ya Pan1, Jun Chen1

  • 1MOE Key Laboratory of Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou 310058, China.

Insights

DNA double-strand breaks (DSBs) can cause mutations and cancer. The p53 gene family, including various p53 isoforms, plays a crucial role in repairing these DNA damages to maintain genomic stability.

Area of Science:

  • Molecular Biology
  • Genetics
  • Cancer Research

Background:

  • DNA double-strand breaks (DSBs) are severe genotoxic damages.
  • Improper DSB repair leads to genetic instability, mutations, and cancer.
  • The tumor suppressor p53 is critical in DNA damage response and frequently mutated in human cancers.

Purpose of the Study:

  • To review the functions of the p53 gene family members and their isoforms.
  • To explore the role of p53 and its isoforms in DNA double-strand break repair.

Main Methods:

  • Literature review of studies on p53 family members and DNA repair.
  • Analysis of the roles of different p53 isoforms in cellular response to DNA damage.

Main Results:

  • The p53 gene family comprises p53, p63, and p73.
  • The human p53 gene encodes at least 12 isoforms.
  • Different p53 members and isoforms exhibit distinct functions in DNA damage response and repair.

Conclusions:

  • The p53 family, through its diverse isoforms, is essential for maintaining genomic integrity following DNA DSBs.
  • Understanding p53 isoform functions is crucial for developing therapeutic strategies against cancer and other diseases linked to genomic instability.

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