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Missing the Mark: PRDM9-Dependent Methylation Is Required for Meiotic DSB Targeting.
Kang, Rhea; Zelazowski, Maciej J; Cole, Francesca.
Afiliación
  • Kang R; Department of Epigenetics and Molecular Carcinogenesis, University of Texas MD Anderson Cancer Center, Science Park, Smithville, TX 78957, USA; Program in Genetics and Epigenetics, MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Science Park, Smithville, TX 78957, USA.
  • Zelazowski MJ; Department of Epigenetics and Molecular Carcinogenesis, University of Texas MD Anderson Cancer Center, Science Park, Smithville, TX 78957, USA.
  • Cole F; Department of Epigenetics and Molecular Carcinogenesis, University of Texas MD Anderson Cancer Center, Science Park, Smithville, TX 78957, USA; Program in Genetics and Epigenetics, MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Science Park, Smithville, TX 78957, USA. Electronic address: fcole@mdanderson.org.
Mol Cell ; 69(5): 725-727, 2018 03 01.
Article en En | MEDLINE | ID: mdl-29499130
ABSTRACT
PRDM9 determines the localization of meiotic recombination hotspots, which are associated with histone H3 methylation. It is not known whether PRDM9's methyltransferase activity is required or how some PRDM9 alleles can dominate the distribution of hotspots over other alleles. Diagouraga, Clément, and colleagues (2018) show that methyltransferase activity is required for hotspot localization and that this activity is additive in combination, suggesting that the dominance of particular alleles is simply proportional to the frequency of targeted sites.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sitios de Unión / Metiltransferasas Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sitios de Unión / Metiltransferasas Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2018 Tipo del documento: Article