Sporadic DUX4 expression in FSHD myocytes is associated with incomplete repression by the PRC2 complex and gain of H3K9 acetylation on the contracted D4Z4 allele

BACKGROUND: Facioscapulohumeral muscular dystrophy 1 (FSHD1) has an autosomal dominant pattern of inheritance and primarily affects skeletal muscle. The genetic cause of FSHD1 is contraction of the D4Z4 macrosatellite array on chromosome 4 alleles associated with a permissive haplotype causing infre...

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Detalles Bibliográficos
Autores principales: Haynes, Premi, Bomsztyk, Karol, Miller, Daniel G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100714/
https://www.ncbi.nlm.nih.gov/pubmed/30122154
http://dx.doi.org/10.1186/s13072-018-0215-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100714/
https://www.ncbi.nlm.nih.gov/pubmed/30122154
http://dx.doi.org/10.1186/s13072-018-0215-z

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