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Human DNA methylomes of neurodegenerative diseases show common epigenomic patterns.
Sanchez-Mut, J V; Heyn, H; Vidal, E; Moran, S; Sayols, S; Delgado-Morales, R; Schultz, M D; Ansoleaga, B; Garcia-Esparcia, P; Pons-Espinal, M; de Lagran, M M; Dopazo, J; Rabano, A; Avila, J; Dierssen, M; Lott, I; Ferrer, I; Ecker, J R; Esteller, M.
Afiliação
  • Sanchez-Mut JV; Epigenetics and Biology Program, Bellvitge Biomedical Research Institute, Barcelona, Spain.
  • Heyn H; Epigenetics and Biology Program, Bellvitge Biomedical Research Institute, Barcelona, Spain.
  • Vidal E; Epigenetics and Biology Program, Bellvitge Biomedical Research Institute, Barcelona, Spain.
  • Moran S; Epigenetics and Biology Program, Bellvitge Biomedical Research Institute, Barcelona, Spain.
  • Sayols S; Epigenetics and Biology Program, Bellvitge Biomedical Research Institute, Barcelona, Spain.
  • Delgado-Morales R; Epigenetics and Biology Program, Bellvitge Biomedical Research Institute, Barcelona, Spain.
  • Schultz MD; Genomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA, USA.
  • Ansoleaga B; Bioinformatics Program, University of California at San Diego, La Jolla, CA, USA.
  • Garcia-Esparcia P; Neuropathology Institute, Bellvitge Biomedical Research Institute-Hospital Universitari de Bellvitge, Universitat de Barcelona, Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, Barcelona, Spain.
  • Pons-Espinal M; Neuropathology Institute, Bellvitge Biomedical Research Institute-Hospital Universitari de Bellvitge, Universitat de Barcelona, Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, Barcelona, Spain.
  • de Lagran MM; Centre for Genomic Regulation, Universitat Pompeu Fabra, Barcelona, Spain.
  • Dopazo J; Centro de Investigación Biomédica en Red de Enfermedades Raras, Barcelona, Spain.
  • Rabano A; Centre for Genomic Regulation, Universitat Pompeu Fabra, Barcelona, Spain.
  • Avila J; Centro de Investigación Biomédica en Red de Enfermedades Raras, Barcelona, Spain.
  • Dierssen M; Computational Genomics Department, Centro de Investigación Príncipe Felipe, Valencia, Spain.
  • Lott I; Neuropathology Laboratory, Research Unit Alzheimer's Project, Fundación CIEN, Madrid, Spain.
  • Ferrer I; Department of Neuroscience, Centro de Biología Molecular Severo Ochoa CSIC/UAM, Universidad Autónoma de Madrid, Madrid, Spain.
  • Ecker JR; Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, Madrid, Spain.
  • Esteller M; Centre for Genomic Regulation, Universitat Pompeu Fabra, Barcelona, Spain.
Transl Psychiatry ; 6: e718, 2016 Jan 19.
Article em En | MEDLINE | ID: mdl-26784972
ABSTRACT
Different neurodegenerative disorders often show similar lesions, such as the presence of amyloid plaques, TAU-neurotangles and synuclein inclusions. The genetically inherited forms are rare, so we wondered whether shared epigenetic aberrations, such as those affecting DNA methylation, might also exist. The studied samples were gray matter samples from the prefrontal cortex of control and neurodegenerative disease-associated cases. We performed the DNA methylation analyses of Alzheimer's disease, dementia with Lewy bodies, Parkinson's disease and Alzheimer-like neurodegenerative profile associated with Down's syndrome samples. The DNA methylation landscapes obtained show that neurodegenerative diseases share similar aberrant CpG methylation shifts targeting a defined gene set. Our findings suggest that neurodegenerative disorders might have similar pathogenetic mechanisms that subsequently evolve into different clinical entities. The identified aberrant DNA methylation changes can be used as biomarkers of the disorders and as potential new targets for the development of new therapies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Córtex Pré-Frontal / Metilação de DNA / Doenças Neurodegenerativas / Epigenômica Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Transl Psychiatry Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Córtex Pré-Frontal / Metilação de DNA / Doenças Neurodegenerativas / Epigenômica Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Transl Psychiatry Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Espanha