Transcriptome-scale spatial gene expression in the human dorsolateral prefrontal cortex

We used the 10x Genomics Visium platform to define the spatial topography of gene expression in the six-layered human dorsolateral prefrontal cortex (DLPFC). We identified extensive layer-enriched expression signatures, and refined associations to previous laminar markers. We overlaid our laminar ex...

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Published inbioRxiv
Main Authors Maynard, Kristen E, Collado-Torres, Leonardo, Weber, Lukas M, Uytingco, Cedric, Barry, Brianna K, Williams, Stephen R, Catallini, Joseph L, Tran, Matthew N, Besich, Zachary, Tippani, Madhavi, Chew, Jennifer, Yin, Yifeng, Kleinman, Joel E, Hyde, Thomas M, Rao, Nikhil, Hicks, Stephanie C, Martinowich, Keri, Jaffe, Andrew E
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LanguageEnglish
Published Cold Spring Harbor Cold Spring Harbor Laboratory Press 28.02.2020
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Abstract We used the 10x Genomics Visium platform to define the spatial topography of gene expression in the six-layered human dorsolateral prefrontal cortex (DLPFC). We identified extensive layer-enriched expression signatures, and refined associations to previous laminar markers. We overlaid our laminar expression signatures onto large-scale single nuclei RNA sequencing data, enhancing spatial annotation of expression-driven clusters. By integrating neuropsychiatric disorder gene sets, we showed differential layer-enriched expression of genes associated with schizophrenia and autism spectrum disorder, highlighting the clinical relevance of spatially-defined expression. We then developed a data-driven framework to define unsupervised clusters in spatial transcriptomics data, which can be applied to other tissues or brain regions where morphological architecture is not as well-defined as cortical laminae. We lastly created a web application for the scientific community to explore these raw and summarized data to augment ongoing neuroscience and spatial transcriptomics research (http://research.libd.org/spatialLIBD) Footnotes * http://research.libd.org/spatialLIBD
AbstractList We used the 10x Genomics Visium platform to define the spatial topography of gene expression in the six-layered human dorsolateral prefrontal cortex (DLPFC). We identified extensive layer-enriched expression signatures, and refined associations to previous laminar markers. We overlaid our laminar expression signatures onto large-scale single nuclei RNA sequencing data, enhancing spatial annotation of expression-driven clusters. By integrating neuropsychiatric disorder gene sets, we showed differential layer-enriched expression of genes associated with schizophrenia and autism spectrum disorder, highlighting the clinical relevance of spatially-defined expression. We then developed a data-driven framework to define unsupervised clusters in spatial transcriptomics data, which can be applied to other tissues or brain regions where morphological architecture is not as well-defined as cortical laminae. We lastly created a web application for the scientific community to explore these raw and summarized data to augment ongoing neuroscience and spatial transcriptomics research (http://research.libd.org/spatialLIBD) Footnotes * http://research.libd.org/spatialLIBD
Author Yin, Yifeng
Hicks, Stephanie C
Uytingco, Cedric
Chew, Jennifer
Hyde, Thomas M
Tippani, Madhavi
Martinowich, Keri
Weber, Lukas M
Williams, Stephen R
Collado-Torres, Leonardo
Maynard, Kristen E
Barry, Brianna K
Tran, Matthew N
Jaffe, Andrew E
Catallini, Joseph L
Besich, Zachary
Kleinman, Joel E
Rao, Nikhil
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Snippet We used the 10x Genomics Visium platform to define the spatial topography of gene expression in the six-layered human dorsolateral prefrontal cortex (DLPFC)....
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SubjectTerms Autism
Brain architecture
Gene expression
Genomics
Mental disorders
Nervous system
Prefrontal cortex
Ribonucleic acid
RNA
Schizophrenia
Transcriptomics
Title Transcriptome-scale spatial gene expression in the human dorsolateral prefrontal cortex
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