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Arabidopsis AtMORC4 and AtMORC7 Form Nuclear Bodies and Repress a Large Number of Protein-Coding Genes.
Harris, C Jake; Husmann, Dylan; Liu, Wanlu; Kasmi, Farid El; Wang, Haifeng; Papikian, Ashot; Pastor, William A; Moissiard, Guillaume; Vashisht, Ajay A; Dangl, Jeffery L; Wohlschlegel, James A; Jacobsen, Steven E.
Afiliação
  • Harris CJ; Department of Molecular, Cell and Developmental Biology, University of California at Los Angeles, Los Angeles, California, United States of America.
  • Husmann D; Department of Molecular, Cell and Developmental Biology, University of California at Los Angeles, Los Angeles, California, United States of America.
  • Liu W; Department of Molecular, Cell and Developmental Biology, University of California at Los Angeles, Los Angeles, California, United States of America.
  • Kasmi FE; Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Wang H; Basic Forestry and Proteomics Research Center, Haixia Institute of Science and Technology (HIST), Fujian Agriculture and Forestry University, Fuzhou, Fujian, China.
  • Papikian A; Fujian Province Key Laboratory of Plant Virology, Institute of Plant Virology, Fujian Agriculture and Forestry University, Fuzhou, Fujian, China.
  • Pastor WA; Department of Molecular, Cell and Developmental Biology, University of California at Los Angeles, Los Angeles, California, United States of America.
  • Moissiard G; Department of Molecular, Cell and Developmental Biology, University of California at Los Angeles, Los Angeles, California, United States of America.
  • Vashisht AA; Department of Molecular, Cell and Developmental Biology, University of California at Los Angeles, Los Angeles, California, United States of America.
  • Dangl JL; Department of Biological Chemistry, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, United States of America.
  • Wohlschlegel JA; Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Jacobsen SE; Howard Hughes Medical Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
PLoS Genet ; 12(5): e1005998, 2016 05.
Article em En | MEDLINE | ID: mdl-27171361
ABSTRACT
The MORC family of GHKL ATPases are an enigmatic class of proteins with diverse chromatin related functions. In Arabidopsis, AtMORC1, AtMORC2, and AtMORC6 act together in heterodimeric complexes to mediate transcriptional silencing of methylated DNA elements. Here, we studied Arabidopsis AtMORC4 and AtMORC7. We found that, in contrast to AtMORC1,2,6, they act to suppress a wide set of non-methylated protein-coding genes that are enriched for those involved in pathogen response. Furthermore, atmorc4 atmorc7 double mutants show a pathogen response phenotype. We found that AtMORC4 and AtMORC7 form homomeric complexes in vivo and are concentrated in discrete nuclear bodies adjacent to chromocenters. Analysis of an atmorc1,2,4,5,6,7 hextuple mutant demonstrates that transcriptional de-repression is largely uncoupled from changes in DNA methylation in plants devoid of MORC function. However, we also uncover a requirement for MORC in both DNA methylation and silencing at a small but distinct subset of RNA-directed DNA methylation target loci. These regions are characterized by poised transcriptional potential and a low density of sites for symmetric cytosine methylation. These results provide insight into the biological function of MORC proteins in higher eukaryotes.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transcrição Gênica / Adenosina Trifosfatases / Proteínas de Arabidopsis / Epigênese Genética Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transcrição Gênica / Adenosina Trifosfatases / Proteínas de Arabidopsis / Epigênese Genética Idioma: En Ano de publicação: 2016 Tipo de documento: Article