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SETD2 safeguards the genome against isochromosome formation.
Mason, Frank M; Kounlavong, Emily S; Tebeje, Anteneh T; Dahiya, Rashmi; Guess, Tiffany; Khan, Abid; Vlach, Logan; Norris, Stephen R; Lovejoy, Courtney A; Dere, Ruhee; Strahl, Brian D; Ohi, Ryoma; Ly, Peter; Walker, Cheryl Lyn; Rathmell, W Kimryn.
Afiliación
  • Mason FM; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232.
  • Kounlavong ES; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232.
  • Tebeje AT; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232.
  • Dahiya R; Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
  • Guess T; Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232.
  • Khan A; Department of Biochemistry and Biophysics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
  • Vlach L; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232.
  • Norris SR; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232.
  • Lovejoy CA; Department of Biochemistry, Vanderbilt University, Nashville, TN 37232.
  • Dere R; Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030.
  • Strahl BD; Department of Biochemistry and Biophysics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
  • Ohi R; Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.
  • Ly P; Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
  • Walker CL; Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030.
  • Rathmell WK; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232.
Proc Natl Acad Sci U S A ; 120(39): e2303752120, 2023 09 26.
Article en En | MEDLINE | ID: mdl-37722039
ABSTRACT
Isochromosomes are mirror-imaged chromosomes with simultaneous duplication and deletion of genetic material which may contain two centromeres to create isodicentric chromosomes. Although isochromosomes commonly occur in cancer and developmental disorders and promote genome instability, mechanisms that prevent isochromosomes are not well understood. We show here that the tumor suppressor and methyltransferase SETD2 is essential to prevent these errors. Using cellular and cytogenetic approaches, we demonstrate that loss of SETD2 or its epigenetic mark, histone H3 lysine 36 trimethylation (H3K36me3), results in the formation of isochromosomes as well as isodicentric and acentric chromosomes. These defects arise during DNA replication and are likely due to faulty homologous recombination by RAD52. These data provide a mechanism for isochromosome generation and demonstrate that SETD2 and H3K36me3 are essential to prevent the formation of this common mutable chromatin structure known to initiate a cascade of genomic instability in cancer.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Isocromosomas Límite: Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Isocromosomas Límite: Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2023 Tipo del documento: Article