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Nucleosome positioning is unaltered at MLH1 splice site mutations in cells derived from Lynch syndrome patients
BACKGROUND: Splicing is more efficient when coupled with transcription and it has been proposed that nucleosomes enriched in exons are important for splice site recognition. Lynch syndrome is a familial cancer syndrome that can be caused by the autosomal dominant inheritance of splice site mutations...
Autores principales: | Sloane, Mathew A, Hesson, Luke B, Nunez, Andrea C, Thompson, Bryony A, Ward, Robyn L |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4272815/ https://www.ncbi.nlm.nih.gov/pubmed/25530820 http://dx.doi.org/10.1186/s13148-014-0032-6 |
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