类有机物
生物
诱导多能干细胞
细胞分化
细胞生物学
表观基因组
细胞命运测定
转录组
干细胞
增强子
染色质
电池类型
定向微分
细胞
转录因子
胚胎干细胞
遗传学
基因
基因表达
DNA甲基化
作者
Yasuhiro Yoshimura,Yoshiharu Muto,Nicolas Ledru,Hao Wu,Kohei Omachi,Jeffrey H. Miner,Benjamin D. Humphreys
标识
DOI:10.1073/pnas.2219699120
摘要
Kidney organoids differentiated from pluripotent stem cells are powerful models of kidney development and disease but are characterized by cell immaturity and off-target cell fates. Comparing the cell-specific gene regulatory landscape during organoid differentiation with human adult kidney can serve to benchmark progress in differentiation at the epigenome and transcriptome level for individual organoid cell types. Using single-cell multiome and histone modification analysis, we report more broadly open chromatin in organoid cell types compared to the human adult kidney. We infer enhancer dynamics by cis-coaccessibility analysis and validate an enhancer driving transcription of HNF1B by CRISPR interference both in cultured proximal tubule cells and also during organoid differentiation. Our approach provides an experimental framework to judge the cell-specific maturation state of human kidney organoids and shows that kidney organoids can be used to validate individual gene regulatory networks that regulate differentiation.
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