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Identification of a DNA N6-Adenine Methyltransferase Complex and Its Impact on Chromatin Organization.
Beh, Leslie Y; Debelouchina, Galia T; Clay, Derek M; Thompson, Robert E; Lindblad, Kelsi A; Hutton, Elizabeth R; Bracht, John R; Sebra, Robert P; Muir, Tom W; Landweber, Laura F.
Afiliación
  • Beh LY; Departments of Biochemistry & Molecular Biophysics and Biological Sciences, Columbia University, New York, NY 10032, USA; Department of Chemistry, Princeton University, Princeton, NJ 08544, USA; Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ 08544, USA.
  • Debelouchina GT; Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.
  • Clay DM; Departments of Biochemistry & Molecular Biophysics and Biological Sciences, Columbia University, New York, NY 10032, USA.
  • Thompson RE; Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.
  • Lindblad KA; Departments of Biochemistry & Molecular Biophysics and Biological Sciences, Columbia University, New York, NY 10032, USA.
  • Hutton ER; Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ 08544, USA.
  • Bracht JR; Department of Biology, American University, Washington, DC 20016, USA.
  • Sebra RP; Icahn Institute and Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Muir TW; Department of Chemistry, Princeton University, Princeton, NJ 08544, USA. Electronic address: muir@princeton.edu.
  • Landweber LF; Departments of Biochemistry & Molecular Biophysics and Biological Sciences, Columbia University, New York, NY 10032, USA. Electronic address: laura.landweber@columbia.edu.
Cell ; 177(7): 1781-1796.e25, 2019 06 13.
Article en En | MEDLINE | ID: mdl-31104845
ABSTRACT
DNA N6-adenine methylation (6mA) has recently been described in diverse eukaryotes, spanning unicellular organisms to metazoa. Here, we report a DNA 6mA methyltransferase complex in ciliates, termed MTA1c. It consists of two MT-A70 proteins and two homeobox-like DNA-binding proteins and specifically methylates dsDNA. Disruption of the catalytic subunit, MTA1, in the ciliate Oxytricha leads to genome-wide loss of 6mA and abolishment of the consensus ApT dimethylated motif. Mutants fail to complete the sexual cycle, which normally coincides with peak MTA1 expression. We investigate the impact of 6mA on nucleosome occupancy in vitro by reconstructing complete, full-length Oxytricha chromosomes harboring 6mA in native or ectopic positions. We show that 6mA directly disfavors nucleosomes in vitro in a local, quantitative manner, independent of DNA sequence. Furthermore, the chromatin remodeler ACF can overcome this effect. Our study identifies a diverged DNA N6-adenine methyltransferase and defines the role of 6mA in chromatin organization.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Nucleosomas / Metiltransferasa de ADN de Sitio Específico (Adenina Especifica) / Proteínas Protozoarias / Tetrahymena thermophila / Oxytricha / Complejos Multienzimáticos Tipo de estudio: Diagnostic_studies Idioma: En Revista: Cell Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Nucleosomas / Metiltransferasa de ADN de Sitio Específico (Adenina Especifica) / Proteínas Protozoarias / Tetrahymena thermophila / Oxytricha / Complejos Multienzimáticos Tipo de estudio: Diagnostic_studies Idioma: En Revista: Cell Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos