Human gene expression variability and its dependence on methylation and aging

Abstract Background Phenotypic variability of human populations is partly the result of gene polymorphism and differential gene expression. As such, understanding the molecular basis for diversity requires identifying genes with both high and low population expression variance and identifying the me...

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Main Authors: Nasser Bashkeel, Theodore J. Perkins, Mads Kærn, Jonathan M. Lee
Format: Article
Language:English
Published: BMC 2019-12-01
Series:BMC Genomics
Subjects:
Online Access:https://doi.org/10.1186/s12864-019-6308-7
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spelling doaj-8008a172817b473b886a6e0d248fbe652020-12-06T12:25:05ZengBMCBMC Genomics1471-21642019-12-0120111910.1186/s12864-019-6308-7Human gene expression variability and its dependence on methylation and agingNasser Bashkeel0Theodore J. Perkins1Mads Kærn2Jonathan M. Lee3Department of Biochemistry, Microbiology, and Immunology, University of OttawaOttawa Hospital Research InstituteDepartment of Cellular and Molecular Medicine, University of OttawaDepartment of Biochemistry, Microbiology, and Immunology, University of OttawaAbstract Background Phenotypic variability of human populations is partly the result of gene polymorphism and differential gene expression. As such, understanding the molecular basis for diversity requires identifying genes with both high and low population expression variance and identifying the mechanisms underlying their expression control. Key issues remain unanswered with respect to expression variability in human populations. The role of gene methylation as well as the contribution that age, sex and tissue-specific factors have on expression variability are not well understood. Results Here we used a novel method that accounts for sampling error to classify human genes based on their expression variability in normal human breast and brain tissues. We find that high expression variability is almost exclusively unimodal, indicating that variance is not the result of segregation into distinct expression states. Genes with high expression variability differ markedly between tissues and we find that genes with high population expression variability are likely to have age-, but not sex-dependent expression. Lastly, we find that methylation likely has a key role in controlling expression variability insofar as genes with low expression variability are likely to be non-methylated. Conclusions We conclude that gene expression variability in the human population is likely to be important in tissue development and identity, methylation, and in natural biological aging. The expression variability of a gene is an important functional characteristic of the gene itself and the classification of a gene as one with Hyper-Variability or Hypo-Variability in a human population or in a specific tissue should be useful in the identification of important genes that functionally regulate development or disease.https://doi.org/10.1186/s12864-019-6308-7Expression variabilityTissue specificityEssentialityMethylationAging
collection DOAJ
language English
format Article
sources DOAJ
author Nasser Bashkeel
Theodore J. Perkins
Mads Kærn
Jonathan M. Lee
spellingShingle Nasser Bashkeel
Theodore J. Perkins
Mads Kærn
Jonathan M. Lee
Human gene expression variability and its dependence on methylation and aging
BMC Genomics
Expression variability
Tissue specificity
Essentiality
Methylation
Aging
author_facet Nasser Bashkeel
Theodore J. Perkins
Mads Kærn
Jonathan M. Lee
author_sort Nasser Bashkeel
title Human gene expression variability and its dependence on methylation and aging
title_short Human gene expression variability and its dependence on methylation and aging
title_full Human gene expression variability and its dependence on methylation and aging
title_fullStr Human gene expression variability and its dependence on methylation and aging
title_full_unstemmed Human gene expression variability and its dependence on methylation and aging
title_sort human gene expression variability and its dependence on methylation and aging
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2019-12-01
description Abstract Background Phenotypic variability of human populations is partly the result of gene polymorphism and differential gene expression. As such, understanding the molecular basis for diversity requires identifying genes with both high and low population expression variance and identifying the mechanisms underlying their expression control. Key issues remain unanswered with respect to expression variability in human populations. The role of gene methylation as well as the contribution that age, sex and tissue-specific factors have on expression variability are not well understood. Results Here we used a novel method that accounts for sampling error to classify human genes based on their expression variability in normal human breast and brain tissues. We find that high expression variability is almost exclusively unimodal, indicating that variance is not the result of segregation into distinct expression states. Genes with high expression variability differ markedly between tissues and we find that genes with high population expression variability are likely to have age-, but not sex-dependent expression. Lastly, we find that methylation likely has a key role in controlling expression variability insofar as genes with low expression variability are likely to be non-methylated. Conclusions We conclude that gene expression variability in the human population is likely to be important in tissue development and identity, methylation, and in natural biological aging. The expression variability of a gene is an important functional characteristic of the gene itself and the classification of a gene as one with Hyper-Variability or Hypo-Variability in a human population or in a specific tissue should be useful in the identification of important genes that functionally regulate development or disease.
topic Expression variability
Tissue specificity
Essentiality
Methylation
Aging
url https://doi.org/10.1186/s12864-019-6308-7
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