A single-cell massively parallel reporter assay detects cell-type-specific gene regulation

被引:35
|
作者
Zhao, Siqi [1 ,2 ,4 ]
Hong, Clarice K. Y. [1 ,2 ]
Myers, Connie A. [3 ]
Granas, David M. [1 ,2 ]
White, Michael A. [1 ,2 ]
Corbo, Joseph C. [3 ]
Cohen, Barak A. [1 ,2 ]
机构
[1] Washington Univ, Edison Family Ctr Syst Biol & Genome Sci, Sch Med, St Louis, MO 63110 USA
[2] Washington Univ, Dept Genet, Sch Med, St Louis, MO 63110 USA
[3] Washington Univ, Dept Pathol & Immunol, Sch Med, St Louis, MO USA
[4] Ginkgo Bioworks, Boston, MA USA
基金
美国国家卫生研究院;
关键词
VARIANTS; DISSECTION; EXPRESSION; ENHANCERS;
D O I
10.1038/s41588-022-01278-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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.
引用
收藏
页码:346 / +
页数:20
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