生物
报告基因
电池类型
细胞
计算生物学
基因
HEK 293细胞
巨量平行
遗传学
单细胞分析
K562细胞
调节顺序
胚胎干细胞
基因表达调控
细胞生物学
基因表达
计算机科学
并行计算
作者
Siqi Zhao,Clarice KY Hong,Connie A. Myers,David M. Granas,Michael A. White,Joseph C. Corbo,Barak A. Cohen
出处
期刊:Nature Genetics
[Nature Portfolio]
日期:2023-01-12
卷期号:55 (2): 346-354
被引量:50
标识
DOI:10.1038/s41588-022-01278-7
摘要
Massively parallel reporter gene assays are key tools in regulatory genomics but cannot be used to identify cell-type-specific regulatory elements without performing assays serially across different cell types. To address this problem, we developed a single-cell massively parallel reporter assay (scMPRA) to measure the activity of libraries of cis-regulatory sequences (CRSs) across multiple cell types simultaneously. We assayed a library of core promoters in a mixture of HEK293 and K562 cells and showed that scMPRA is a reproducible, highly parallel, single-cell reporter gene assay that detects cell-type-specific cis-regulatory activity. We then measured a library of promoter variants across multiple cell types in live mouse retinas and showed that subtle genetic variants can produce cell-type-specific effects on cis-regulatory activity. We anticipate that scMPRA will be widely applicable for studying the role of CRSs across diverse cell types.
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