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 Kit Yee Hong,Connie A. Myers,David M Granas,Michael A. White,Joseph C. Corbo,Barak A. Cohen
出处
期刊:Nature Genetics
[Springer Nature]
日期:2023-01-12
卷期号:55 (2): 346-354
被引量:16
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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