4.8 Article

Programmable RNA sensing for cell monitoring and manipulation

Journal

NATURE
Volume 610, Issue 7933, Pages 713-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-022-05280-1

Keywords

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Funding

  1. NIMH [1DP1MH129954-01, 5U19MH114821-03]
  2. NINDS K12 Neurosurgery Research Career Development Program K12 Award
  3. Klingenstein-Simons Foundation

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CellREADR is a RNA-sensing technology that combines RNA detection with protein translation through RNA editing. It allows specific access to cell types in mice, rats, and human brain tissues, and enables the recording and control of specific types of neurons.
RNA is a central and universal mediator of genetic information underlying the diversity of cell types and cell states, which together shape tissue organization and organismal function across species and lifespans. Despite numerous advances in RNA sequencing technologies and the massive accumulation of transcriptome datasets across the life sciences(1,2), the dearth of technologies that use RNAs to observe and manipulate cell types remains a bottleneck in biology and medicine. Here we describe CellREADR (Cell access through RNA sensing by Endogenous ADAR), a programmable RNA-sensing technology that leverages RNA editing mediated by ADAR to couple the detection of cell-defining RNAs with the translation of effector proteins. Viral delivery of CellREADR conferred specific cell-type access in mouse and rat brains and in ex vivo human brain tissues. Furthermore, CellREADR enabled the recording and control of specific types of neurons in behaving mice. CellREADR thus highlights the potential for RNA-based monitoring and editing of animal cells in ways that are specific, versatile, simple and generalizable across organ systems and species, with wide applications in biology, biotechnology and programmable RNA medicine.

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