Evolutionary conservation and divergence of the human brain transcriptome

Abstract Background Mouse models have allowed for the direct interrogation of genetic effects on molecular, physiological, and behavioral brain phenotypes. However, it is unknown to what extent neurological or psychiatric traits may be human- or primate-specific and therefore which components can be...

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Main Authors: William G. Pembroke, Christopher L. Hartl, Daniel H. Geschwind
Format: Article
Language:English
Published: BMC 2021-01-01
Series:Genome Biology
Subjects:
Online Access:https://doi.org/10.1186/s13059-020-02257-z
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spelling doaj-85c1b5c927d943e5960896a8aaceedbc2021-01-31T16:37:44ZengBMCGenome Biology1474-760X2021-01-0122113310.1186/s13059-020-02257-zEvolutionary conservation and divergence of the human brain transcriptomeWilliam G. Pembroke0Christopher L. Hartl1Daniel H. Geschwind2Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, UCLAProgram in Neurogenetics, Department of Neurology, David Geffen School of Medicine, UCLAProgram in Neurogenetics, Department of Neurology, David Geffen School of Medicine, UCLAAbstract Background Mouse models have allowed for the direct interrogation of genetic effects on molecular, physiological, and behavioral brain phenotypes. However, it is unknown to what extent neurological or psychiatric traits may be human- or primate-specific and therefore which components can be faithfully recapitulated in mouse models. Results We compare conservation of co-expression in 116 independent data sets derived from human, mouse, and non-human primate representing more than 15,000 total samples. We observe greater changes occurring on the human lineage than mouse, and substantial regional variation that highlights cerebral cortex as the most diverged region. Glia, notably microglia, astrocytes, and oligodendrocytes are the most divergent cell type, three times more on average than neurons. We show that cis-regulatory sequence divergence explains a significant fraction of co-expression divergence. Moreover, protein coding sequence constraint parallels co-expression conservation, such that genes with loss of function intolerance are enriched in neuronal, rather than glial modules. We identify dozens of human neuropsychiatric and neurodegenerative disease risk genes, such as COMT, PSEN-1, LRRK2, SHANK3, and SNCA, with highly divergent co-expression between mouse and human and show that 3D human brain organoids recapitulate in vivo co-expression modules representing several human cell types. Conclusions We identify robust co-expression modules reflecting whole-brain and regional patterns of gene expression. Compared with those that represent basic metabolic processes, cell-type-specific modules, most prominently glial modules, are the most divergent between species. These data and analyses serve as a foundational resource to guide human disease modeling and its interpretation.https://doi.org/10.1186/s13059-020-02257-zEvolutionGenomicsTranscriptomeCo-expressionNeuroscienceDisease
collection DOAJ
language English
format Article
sources DOAJ
author William G. Pembroke
Christopher L. Hartl
Daniel H. Geschwind
spellingShingle William G. Pembroke
Christopher L. Hartl
Daniel H. Geschwind
Evolutionary conservation and divergence of the human brain transcriptome
Genome Biology
Evolution
Genomics
Transcriptome
Co-expression
Neuroscience
Disease
author_facet William G. Pembroke
Christopher L. Hartl
Daniel H. Geschwind
author_sort William G. Pembroke
title Evolutionary conservation and divergence of the human brain transcriptome
title_short Evolutionary conservation and divergence of the human brain transcriptome
title_full Evolutionary conservation and divergence of the human brain transcriptome
title_fullStr Evolutionary conservation and divergence of the human brain transcriptome
title_full_unstemmed Evolutionary conservation and divergence of the human brain transcriptome
title_sort evolutionary conservation and divergence of the human brain transcriptome
publisher BMC
series Genome Biology
issn 1474-760X
publishDate 2021-01-01
description Abstract Background Mouse models have allowed for the direct interrogation of genetic effects on molecular, physiological, and behavioral brain phenotypes. However, it is unknown to what extent neurological or psychiatric traits may be human- or primate-specific and therefore which components can be faithfully recapitulated in mouse models. Results We compare conservation of co-expression in 116 independent data sets derived from human, mouse, and non-human primate representing more than 15,000 total samples. We observe greater changes occurring on the human lineage than mouse, and substantial regional variation that highlights cerebral cortex as the most diverged region. Glia, notably microglia, astrocytes, and oligodendrocytes are the most divergent cell type, three times more on average than neurons. We show that cis-regulatory sequence divergence explains a significant fraction of co-expression divergence. Moreover, protein coding sequence constraint parallels co-expression conservation, such that genes with loss of function intolerance are enriched in neuronal, rather than glial modules. We identify dozens of human neuropsychiatric and neurodegenerative disease risk genes, such as COMT, PSEN-1, LRRK2, SHANK3, and SNCA, with highly divergent co-expression between mouse and human and show that 3D human brain organoids recapitulate in vivo co-expression modules representing several human cell types. Conclusions We identify robust co-expression modules reflecting whole-brain and regional patterns of gene expression. Compared with those that represent basic metabolic processes, cell-type-specific modules, most prominently glial modules, are the most divergent between species. These data and analyses serve as a foundational resource to guide human disease modeling and its interpretation.
topic Evolution
Genomics
Transcriptome
Co-expression
Neuroscience
Disease
url https://doi.org/10.1186/s13059-020-02257-z
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