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The ATRX-ADD domain binds to H3 tail peptides and reads the combined methylation state of K4 and K9

Mutations in the ATRX protein are associated with the alpha-thalassemia and mental retardation X-linked syndrome (ATR-X). Almost half of the disease-causing mutations occur in its ATRX-Dnmt3-Dnmt3L (ADD) domain. By employing peptide arrays, chromatin pull-down and peptide binding assays, we show spe...

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Détails bibliographiques
Auteurs principaux: Dhayalan, Arunkumar, Tamas, Raluca, Bock, Ina, Tattermusch, Anna, Dimitrova, Emilia, Kudithipudi, Srikanth, Ragozin, Sergey, Jeltsch, Albert
Format: Artigo
Langue:Inglês
Publié: Oxford University Press 2011
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3090196/
https://ncbi.nlm.nih.gov/pubmed/21421568
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr107
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