Cell reports · 2022
Genome-wide fetalization of enhancer architecture in heart disease.
СтатьяПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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Spurrell Cailyn H, Barozzi Iros, Kosicki Michael, Mannion Brandon J, Blow Matthew J, Fukuda-Yuzawa Yoko, Slaven Neil, Afzal Sarah Y, Akiyama Jennifer A, Afzal Veena, Tran Stella, Plajzer-Frick Ingrid, Novak Catherine S, Kato Momoe, Lee Elizabeth A, Garvin Tyler H, Pham Quan T, Kronshage Anne N, Lisgo Steven, Bristow James, Cappola Thomas P, Morley Michael P, Margulies Kenneth B, Pennacchio Len A, Dickel Diane E, Visel Axel
Аннотация
Heart disease is associated with re-expression of key transcription factors normally active only during prenatal development of the heart. However, the impact of this reactivation on the regulatory landscape in heart disease is unclear. Here, we use RNA-seq and ChIP-seq targeting a histone modification associated with active transcriptional enhancers to generate genome-wide enhancer maps from left ventricle tissue from up to 26 healthy controls, 18 individuals with idiopathic dilated cardiomyopathy (DCM), and five fetal hearts. Healthy individuals have a highly reproducible epigenomic landscape, consisting of more than 33,000 predicted heart enhancers. In contrast, we observe reproducible disease-associated changes in activity at 6,850 predicted heart enhancers. Combined analysis of adult and fetal samples reveals that the heart disease epigenome and transcriptome both acquire fetal-like characteristics, with 3,400 individual enhancers sharing fetal regulatory properties. We also provide a comprehensive data resource (http://heart.lbl.gov) for the mechanistic exploration of DCM etiology.