Gene Expression Switching of Receptor Subunits in Human Brain Development.

Synaptic receptors in the human brain consist of multiple protein subunits, many of which have multiple variants, coded by different genes, and are differentially expressed across brain regions and developmental stages. The brain can tune the electrophysiological properties of synapses to regulate p...

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Main Authors: Ossnat Bar-Shira, Ronnie Maor, Gal Chechik
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-12-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC4670163?pdf=render
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spelling doaj-e8cd1ab80c324e7d8f467a87ed03f5902020-11-24T21:51:15ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582015-12-011112e100455910.1371/journal.pcbi.1004559Gene Expression Switching of Receptor Subunits in Human Brain Development.Ossnat Bar-ShiraRonnie MaorGal ChechikSynaptic receptors in the human brain consist of multiple protein subunits, many of which have multiple variants, coded by different genes, and are differentially expressed across brain regions and developmental stages. The brain can tune the electrophysiological properties of synapses to regulate plasticity and information processing by switching from one protein variant to another. Such condition-dependent variant switch during development has been demonstrated in several neurotransmitter systems including NMDA and GABA. Here we systematically detect pairs of receptor-subunit variants that switch during the lifetime of the human brain by analyzing postmortem expression data collected in a population of donors at various ages and brain regions measured using microarray and RNA-seq. To further detect variant pairs that co-vary across subjects, we present a method to quantify age-corrected expression correlation in face of strong temporal trends. This is achieved by computing the correlations in the residual expression beyond a cubic-spline model of the population temporal trend, and can be seen as a nonlinear version of partial correlations. Using these methods, we detect multiple new pairs of context dependent variants. For instance, we find a switch from GLRA2 to GLRA3 that differs from the known switch in the rat. We also detect an early switch from HTR1A to HTR5A whose trends are negatively correlated and find that their age-corrected expression is strongly positively correlated. Finally, we observe that GRIN2B switch to GRIN2A occurs mostly during embryonic development, presumably earlier than observed in rodents. These results provide a systematic map of developmental switching in the neurotransmitter systems of the human brain.http://europepmc.org/articles/PMC4670163?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ossnat Bar-Shira
Ronnie Maor
Gal Chechik
spellingShingle Ossnat Bar-Shira
Ronnie Maor
Gal Chechik
Gene Expression Switching of Receptor Subunits in Human Brain Development.
PLoS Computational Biology
author_facet Ossnat Bar-Shira
Ronnie Maor
Gal Chechik
author_sort Ossnat Bar-Shira
title Gene Expression Switching of Receptor Subunits in Human Brain Development.
title_short Gene Expression Switching of Receptor Subunits in Human Brain Development.
title_full Gene Expression Switching of Receptor Subunits in Human Brain Development.
title_fullStr Gene Expression Switching of Receptor Subunits in Human Brain Development.
title_full_unstemmed Gene Expression Switching of Receptor Subunits in Human Brain Development.
title_sort gene expression switching of receptor subunits in human brain development.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2015-12-01
description Synaptic receptors in the human brain consist of multiple protein subunits, many of which have multiple variants, coded by different genes, and are differentially expressed across brain regions and developmental stages. The brain can tune the electrophysiological properties of synapses to regulate plasticity and information processing by switching from one protein variant to another. Such condition-dependent variant switch during development has been demonstrated in several neurotransmitter systems including NMDA and GABA. Here we systematically detect pairs of receptor-subunit variants that switch during the lifetime of the human brain by analyzing postmortem expression data collected in a population of donors at various ages and brain regions measured using microarray and RNA-seq. To further detect variant pairs that co-vary across subjects, we present a method to quantify age-corrected expression correlation in face of strong temporal trends. This is achieved by computing the correlations in the residual expression beyond a cubic-spline model of the population temporal trend, and can be seen as a nonlinear version of partial correlations. Using these methods, we detect multiple new pairs of context dependent variants. For instance, we find a switch from GLRA2 to GLRA3 that differs from the known switch in the rat. We also detect an early switch from HTR1A to HTR5A whose trends are negatively correlated and find that their age-corrected expression is strongly positively correlated. Finally, we observe that GRIN2B switch to GRIN2A occurs mostly during embryonic development, presumably earlier than observed in rodents. These results provide a systematic map of developmental switching in the neurotransmitter systems of the human brain.
url http://europepmc.org/articles/PMC4670163?pdf=render
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