Transcriptomic and epigenomic differences in human induced pluripotent stem cells generated from six reprogramming methods

重编程 诱导多能干细胞 生物 转录组 表观遗传学 胚胎干细胞 表观遗传学 遗传学 人口 H3K4me3 细胞生物学 基因表达 基因 计算生物学 DNA甲基化 发起人 社会学 人口学
作者
Jared M. Churko,Jaecheol Lee,Mohamed Ameen,Mingxia Gu,Meenakshi Venkatasubramanian,Sebastian Diecke,Karim Sallam,Hogune Im,Gavin Wang,Joseph Gold,Nathan Salomonis,M Snyder,Joseph C. Wu
出处
期刊:Nature Biomedical Engineering [Springer Nature]
卷期号:1 (10): 826-837 被引量:46
标识
DOI:10.1038/s41551-017-0141-6
摘要

Many reprogramming methods can generate human induced pluripotent stem cells (hiPSCs) that closely resemble human embryonic stem cells (hESCs). This has led to assessments of how similar hiPSCs are to hESCs, by evaluating differences in gene expression, epigenetic marks and differentiation potential. However, all previous studies were performed using hiPSCs acquired from different laboratories, passage numbers, culturing conditions, genetic backgrounds and reprogramming methods, all of which may contribute to the reported differences. Here, by using high-throughput sequencing under standardized cell culturing conditions and passage number, we compare the epigenetic signatures (H3K4me3, H3K27me3 and HDAC2 ChIP-seq profiles) and transcriptome differences (by RNA-seq) of hiPSCs generated from the same primary fibroblast population by using six different reprogramming methods. We found that the reprogramming method impacts the resulting transcriptome and that all hiPSC lines could terminally differentiate, regardless of the reprogramming method. Moreover, by comparing the differences between the hiPSC and hESC lines, we observed a significant proportion of differentially expressed genes that could be attributed to polycomb repressive complex targets. Epigenetic and transcriptomic differences in human induced pluripotent stem cells generated from the same fibroblast population reveals that the reprogramming method affects the cells' gene-expression levels but not their differentiation potential.
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