TAp73 knockout shows genomic instability with infertility and tumor suppressor functions

Richard Tomasini, Katsuya Tsuchihara, Margareta Wilhelm, Masashi Fujitani, Alessandro Rufini, Carol C. Cheung, Fatima Khan, Annick Itie-Youten, Andrew Wakeham, Ming Sound Tsao, Juan L. Iovanna, Jeremy Squire, Igor Jurisica, David Kaplan, Gerry Melino, Andrea Jurisicova, Tak W. Mak

Research output: Contribution to journalArticlepeer-review


The Trp53 gene family member Trp73 encodes two major groups of protein isoforms, TAp73 and ΔNp73, with opposing pro- and anti-apoptotic functions; consequently, their relative ratio regulates cell fate. However, the precise roles of p73 isoforms in cellular events such as tumor initiation, embryonic development, and cell death remain unclear. To determine which aspects of p73 function are attributable to the TAp73 isoforms, we generated and characterized mice in which exons encoding the TAp73 isoforms were specifically deleted to create a TAp73-deficient (TAp73-/-) mouse. Here we show that mice specifically lacking in TAp73 isoforms develop a phenotype intermediate between the phenotypes of Trp73-/- and Trp53 -/- mice with respect to incidence of spontaneous and carcinogen-induced tumors, infertility, and aging, as well as hippocampal dysgenesis. In addition, cells from TAp73-/- mice exhibit genomic instability associated with enhanced aneuploidy, which may account for the increased incidence of spontaneous tumors observed in these mutants. Hence, TAp73 isoforms exert tumor-suppressive functions and indicate an emerging role for Trp73 in the maintenance of genomic stability.

Original languageEnglish
Pages (from-to)2677-2691
Number of pages15
JournalGenes and Development
Issue number19
Publication statusPublished - Oct 1 2008


  • Genomic instability
  • Infertility
  • Meiosis
  • p73
  • Tumor-prone phenotype

ASJC Scopus subject areas

  • Genetics
  • Developmental Biology


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