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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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 |
work_keys_str_mv |
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