Three-dimensional intact-tissue sequencing of single-cell transcriptional states

Author:

Wang Xiao1ORCID,Allen William E.12ORCID,Wright Matthew A.13ORCID,Sylwestrak Emily L.1,Samusik Nikolay4ORCID,Vesuna Sam1,Evans Kathryn1ORCID,Liu Cindy1ORCID,Ramakrishnan Charu1ORCID,Liu Jia5ORCID,Nolan Garry P.4ORCID,Bava Felice-Alessio4ORCID,Deisseroth Karl136ORCID

Affiliation:

1. Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.

2. Neuroscience Program, Stanford University, CA 94305, USA.

3. Department of Psychiatry and Behavioral Sciences, Stanford University, CA 94305, USA.

4. Baxter Laboratory, Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, USA.

5. Department of Chemical Engineering, Stanford University, CA 94305, USA.

6. Howard Hughes Medical Institute, Stanford University, CA 94305, USA.

Abstract

Transcriptome mapping in the 3D brain RNA sequencing samples the entire transcriptome but lacks anatomical information. In situ hybridization, on the other hand, can only profile a small number of transcripts. In situ sequencing technologies address these shortcomings but face a challenge in dense, complex tissue environments. Wang et al. combined an efficient sequencing approach with hydrogel-tissue chemistry to develop a multidisciplinary technology for three-dimensional (3D) intact-tissue RNA sequencing (see the Perspective by Knöpfel). More than 1000 genes were simultaneously mapped in sections of mouse brain at single-cell resolution to define cell types and circuit states and to reveal cell organization principles. Science , this issue p. eaat5691 ; see also p. 328

Funder

Howard Hughes Medical Institute

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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