表观遗传学
染色质
表观遗传学
生物
组蛋白
计算生物学
人口
转录因子
细胞生物学
遗传学
基因表达
基因
DNA甲基化
医学
环境卫生
作者
Matthew C. Hill,James F. Martin
出处
期刊:Methods in molecular biology
日期:2020-08-28
卷期号:: 307-321
被引量:5
标识
DOI:10.1007/978-1-0716-0668-1_23
摘要
The adult mammalian heart’s potential for regeneration is very inefficient. Importantly, adult mammalian cardiomyocytes (CMs) are characterized as a cell population with very limited mitotic potential. Conversely, the neonatal mouse heart possesses a brief, yet robust, regenerative capacity within the first week of life. Cell type-specific enrichment procedures are essential for characterizing the full spectrum of epigenomic landscapes and gene regulatory networks deployed by mammalian CMs. In this chapter, we describe a protocol useful for purifying CM nuclei from mammalian cardiac tissue. Furthermore, we detail a low-input procedure suitable for the parallel genome-wide profiling of chromatin accessibility, histone modifications, and transcription factor-binding sites. The CM nuclei purified using this process are suitable for multi-omic profiling approaches.
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