AI Article Synopsis

  • The study introduces a single-cell massively parallel reporter assay (scMPRA) that enables the simultaneous measurement of cis-regulatory sequence activity across different cell types, overcoming limitations of previous methods.
  • It demonstrates the effectiveness of scMPRA by analyzing core promoters in HEK293 and K562 cell lines and revealing cell-type-specific regulatory activities.
  • The research highlights that scMPRA can also detect subtle effects of genetic variants on cis-regulatory activity in live mouse retinas, suggesting its broad applicability in regulatory genomics.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931678PMC
http://dx.doi.org/10.1038/s41588-022-01278-7DOI Listing

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