Embryo-scale, single-cell spatial transcriptomics
Spatial patterns of gene expression manifest at scales ranging from local (e.g., cell-cell interactions) to global (e.g., body axis patterning). However, current spatial transcriptomics methods either average local contexts or are restricted to limited fields of view. Here, we introduce sci-Space, w...
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| Vydáno v: | Science (American Association for the Advancement of Science) Ročník 373; číslo 6550; s. 111 |
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| Hlavní autoři: | , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
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United States
02.07.2021
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| ISSN: | 1095-9203, 1095-9203 |
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| Abstract | Spatial patterns of gene expression manifest at scales ranging from local (e.g., cell-cell interactions) to global (e.g., body axis patterning). However, current spatial transcriptomics methods either average local contexts or are restricted to limited fields of view. Here, we introduce sci-Space, which retains single-cell resolution while resolving spatial heterogeneity at larger scales. Applying sci-Space to developing mouse embryos, we captured approximate spatial coordinates and whole transcriptomes of about 120,000 nuclei. We identify thousands of genes exhibiting anatomically patterned expression, leverage spatial information to annotate cellular subtypes, show that cell types vary substantially in their extent of spatial patterning, and reveal correlations between pseudotime and the migratory patterns of differentiating neurons. Looking forward, we anticipate that sci-Space will facilitate the construction of spatially resolved single-cell atlases of mammalian development. |
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| AbstractList | Spatial patterns of gene expression manifest at scales ranging from local (e.g., cell-cell interactions) to global (e.g., body axis patterning). However, current spatial transcriptomics methods either average local contexts or are restricted to limited fields of view. Here, we introduce sci-Space, which retains single-cell resolution while resolving spatial heterogeneity at larger scales. Applying sci-Space to developing mouse embryos, we captured approximate spatial coordinates and whole transcriptomes of about 120,000 nuclei. We identify thousands of genes exhibiting anatomically patterned expression, leverage spatial information to annotate cellular subtypes, show that cell types vary substantially in their extent of spatial patterning, and reveal correlations between pseudotime and the migratory patterns of differentiating neurons. Looking forward, we anticipate that sci-Space will facilitate the construction of spatially resolved single-cell atlases of mammalian development.Spatial patterns of gene expression manifest at scales ranging from local (e.g., cell-cell interactions) to global (e.g., body axis patterning). However, current spatial transcriptomics methods either average local contexts or are restricted to limited fields of view. Here, we introduce sci-Space, which retains single-cell resolution while resolving spatial heterogeneity at larger scales. Applying sci-Space to developing mouse embryos, we captured approximate spatial coordinates and whole transcriptomes of about 120,000 nuclei. We identify thousands of genes exhibiting anatomically patterned expression, leverage spatial information to annotate cellular subtypes, show that cell types vary substantially in their extent of spatial patterning, and reveal correlations between pseudotime and the migratory patterns of differentiating neurons. Looking forward, we anticipate that sci-Space will facilitate the construction of spatially resolved single-cell atlases of mammalian development. Spatial patterns of gene expression manifest at scales ranging from local (e.g., cell-cell interactions) to global (e.g., body axis patterning). However, current spatial transcriptomics methods either average local contexts or are restricted to limited fields of view. Here, we introduce sci-Space, which retains single-cell resolution while resolving spatial heterogeneity at larger scales. Applying sci-Space to developing mouse embryos, we captured approximate spatial coordinates and whole transcriptomes of about 120,000 nuclei. We identify thousands of genes exhibiting anatomically patterned expression, leverage spatial information to annotate cellular subtypes, show that cell types vary substantially in their extent of spatial patterning, and reveal correlations between pseudotime and the migratory patterns of differentiating neurons. Looking forward, we anticipate that sci-Space will facilitate the construction of spatially resolved single-cell atlases of mammalian development. |
| Author | Franks, Jennifer M Duran, Madeleine Shendure, Jay Stevens, Kelly R Barkan, Eliza Packer, Jonathan S Lampe, Paul D Saxton, Sarah Regier, Mary C Ladd, Jon J Spielmann, Malte Srivatsan, Sanjay R Grosjean, Parker Lois, Carlos Trapnell, Cole |
| Author_xml | – sequence: 1 givenname: Sanjay R orcidid: 0000-0001-7282-0487 surname: Srivatsan fullname: Srivatsan, Sanjay R organization: Department of Genome Sciences, University of Washington, Seattle, WA, USA – sequence: 2 givenname: Mary C orcidid: 0000-0001-9074-6604 surname: Regier fullname: Regier, Mary C organization: Institute for Stem Cell and Regenerative Medicine, Seattle, WA, USA – sequence: 3 givenname: Eliza orcidid: 0000-0001-7871-4327 surname: Barkan fullname: Barkan, Eliza organization: Molecular and Cellular Biology Program, University of Washington, Seattle, WA, USA – sequence: 4 givenname: Jennifer M orcidid: 0000-0003-2400-5431 surname: Franks fullname: Franks, Jennifer M organization: Department of Genome Sciences, University of Washington, Seattle, WA, USA – sequence: 5 givenname: Jonathan S orcidid: 0000-0003-4025-0007 surname: Packer fullname: Packer, Jonathan S organization: Foresite Labs, Boston, MA, USA – sequence: 6 givenname: Parker orcidid: 0000-0002-2024-119X surname: Grosjean fullname: Grosjean, Parker organization: Department of Bioengineering. University of Washington, Seattle, WA, USA – sequence: 7 givenname: Madeleine orcidid: 0000-0003-1648-2369 surname: Duran fullname: Duran, Madeleine organization: Department of Genome Sciences, University of Washington, Seattle, WA, USA – sequence: 8 givenname: Sarah orcidid: 0000-0002-3901-4843 surname: Saxton fullname: Saxton, Sarah organization: Department of Bioengineering. University of Washington, Seattle, WA, USA – sequence: 9 givenname: Jon J surname: Ladd fullname: Ladd, Jon J organization: Translational Research Program, Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA – sequence: 10 givenname: Malte orcidid: 0000-0002-0583-4683 surname: Spielmann fullname: Spielmann, Malte organization: Human Molecular Genomics Group, Max Planck Institute for Molecular Genetics, Berlin, Germany – sequence: 11 givenname: Carlos orcidid: 0000-0002-7305-2317 surname: Lois fullname: Lois, Carlos organization: Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA – sequence: 12 givenname: Paul D orcidid: 0000-0002-1399-2761 surname: Lampe fullname: Lampe, Paul D organization: Translational Research Program, Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA – sequence: 13 givenname: Jay orcidid: 0000-0002-1516-1865 surname: Shendure fullname: Shendure, Jay email: shendure@uw.edu, ksteve@uw.edu, coletrap@uw.edu organization: Brotman Baty Institute for Precision Medicine, Seattle, WA, USA – sequence: 14 givenname: Kelly R orcidid: 0000-0002-4024-2990 surname: Stevens fullname: Stevens, Kelly R email: shendure@uw.edu, ksteve@uw.edu, coletrap@uw.edu organization: Department of Laboratory Medicine and Pathology, Seattle, WA, USA – sequence: 15 givenname: Cole orcidid: 0000-0002-8105-4347 surname: Trapnell fullname: Trapnell, Cole email: shendure@uw.edu, ksteve@uw.edu, coletrap@uw.edu organization: Brotman Baty Institute for Precision Medicine, Seattle, WA, USA |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34210887$$D View this record in MEDLINE/PubMed |
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| References | 34750575 - Nat Cell Biol. 2021 Nov;23(11):1108. doi: 10.1038/s41556-021-00778-8 |
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| SubjectTerms | Animals Atlases as Topic Body Patterning - genetics Brain - embryology Cell Movement Embryo, Mammalian - embryology Embryonic Development - genetics Gene Expression Profiling - methods Mice Neurogenesis - genetics Neurons - cytology Single-Cell Analysis - methods Transcriptome |
| Title | Embryo-scale, single-cell spatial transcriptomics |
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