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DNMT1-interacting RNAs block gene-specific DNA methylation.
Di Ruscio, Annalisa; Ebralidze, Alexander K; Benoukraf, Touati; Amabile, Giovanni; Goff, Loyal A; Terragni, Jolyon; Figueroa, Maria Eugenia; De Figueiredo Pontes, Lorena Lobo; Alberich-Jorda, Meritxell; Zhang, Pu; Wu, Mengchu; D'Alò, Francesco; Melnick, Ari; Leone, Giuseppe; Ebralidze, Konstantin K; Pradhan, Sriharsa; Rinn, John L; Tenen, Daniel G.
Afiliação
  • Di Ruscio A; 1] Harvard Stem Cell Institute, Harvard Medical School, Boston, Massachusetts 02115, USA [2] Beth Israel Deaconess Medical Center, Boston, Massachusetts 02115, USA [3] Università Cattolica del Sacro Cuore, Institute of Hematology, L.go A. Gemelli 8, Rome 00168, Italy [4].
Nature ; 503(7476): 371-6, 2013 Nov 21.
Article em En | MEDLINE | ID: mdl-24107992
ABSTRACT
DNA methylation was first described almost a century ago; however, the rules governing its establishment and maintenance remain elusive. Here we present data demonstrating that active transcription regulates levels of genomic methylation. We identify a novel RNA arising from the CEBPA gene locus that is critical in regulating the local DNA methylation profile. This RNA binds to DNMT1 and prevents CEBPA gene locus methylation. Deep sequencing of transcripts associated with DNMT1 combined with genome-scale methylation and expression profiling extend the generality of this finding to numerous gene loci. Collectively, these results delineate the nature of DNMT1-RNA interactions and suggest strategies for gene-selective demethylation of therapeutic targets in human diseases.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulação da Expressão Gênica / Metilação de DNA / Proteínas Estimuladoras de Ligação a CCAAT / RNA não Traduzido / DNA (Citosina-5-)-Metiltransferases Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulação da Expressão Gênica / Metilação de DNA / Proteínas Estimuladoras de Ligação a CCAAT / RNA não Traduzido / DNA (Citosina-5-)-Metiltransferases Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2013 Tipo de documento: Article