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Elephant TP53-RETROGENE 9 induces transcription-independent apoptosis at the mitochondria.
Preston, Aidan J; Rogers, Aaron; Sharp, Miranda; Mitchell, Gareth; Toruno, Cristhian; Barney, Brayden B; Donovan, Lauren N; Bly, Journey; Kennington, Ryan; Payne, Emily; Iovino, Anthony; Furukawa, Gabriela; Robinson, Rosann; Shamloo, Bahar; Buccilli, Matthew; Anders, Rachel; Eckstein, Sarah; Fedak, Elizabeth A; Wright, Tanner; Maley, Carlo C; Kiso, Wendy K; Schmitt, Dennis; Malkin, David; Schiffman, Joshua D; Abegglen, Lisa M.
Afiliação
  • Preston AJ; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Rogers A; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Sharp M; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Mitchell G; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Toruno C; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Barney BB; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Donovan LN; Scripps Green Hospital and Scripps Clinic, La Jolla, CA, USA.
  • Bly J; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Kennington R; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Payne E; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Iovino A; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Furukawa G; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Robinson R; Recursion Pharmaceuticals, Salt Lake City, UT, USA.
  • Shamloo B; Recursion Pharmaceuticals, Salt Lake City, UT, USA.
  • Buccilli M; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Anders R; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Eckstein S; Duke Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA.
  • Fedak EA; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Wright T; Department of Mathematics, University of Utah, Salt Lake City, UT, USA.
  • Maley CC; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
  • Kiso WK; Department of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Schmitt D; Biodesign Institute, School of Life Sciences, and Arizona Cancer Evolution Center, Arizona State University, Tempe, AZ, USA.
  • Malkin D; Colossal Biosciences, Dallas, TX, USA.
  • Schiffman JD; Department of Animal Science, William H. Darr College of Agriculture, Missouri State University, Springfield, MO, USA.
  • Abegglen LM; Division of Haematology/Oncology, The Hospital for Sick Children; Department of Pediatrics, University of Toronto, Toronto, ON, Canada.
Cell Death Discov ; 9(1): 66, 2023 Feb 16.
Article em En | MEDLINE | ID: mdl-36797268
ABSTRACT
Approximately 20 TP53 retrogenes exist in the African and Asian elephant genomes (Loxodonta Africana, Elephas Maximus) in addition to a conserved TP53 gene that encodes a full-length protein. Elephant TP53-RETROGENE 9 (TP53-R9) encodes a p53 protein (p53-R9) that is truncated in the middle of the canonical DNA binding domain. This C-terminally truncated p53 retrogene protein lacks the nuclear localization signals and oligomerization domain of its full-length counterpart. When expressed in human osteosarcoma cells (U2OS), p53-R9 binds to Tid1, the chaperone protein responsible for mitochondrial translocation of human p53 in response to cellular stress. Tid1 expression is required for p53-R9-induced apoptosis. At the mitochondria, p53-R9 binds to the pro-apoptotic BCL-2 family member Bax, which leads to caspase activation, cytochrome c release, and cell death. Our data show, for the first time, that expression of this truncated elephant p53 retrogene protein induces apoptosis in human cancer cells. Understanding the molecular mechanism by which the additional elephant TP53 retrogenes function may provide evolutionary insight that can be utilized for the development of therapeutics to treat human cancers.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article