Cargando…

Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome

Gene expression varies markedly across the menstrual cycle and expression levels for many genes are under genetic control. We analyzed gene expression and mapped expression quantitative trait loci (eQTLs) in endometrial tissue samples from 229 women and then analyzed the overlap of endometrial eQTL...

Descripción completa

Detalles Bibliográficos
Autores principales: Fung, Jenny N., Mortlock, Sally, Girling, Jane E., Holdsworth-Carson, Sarah J., Teh, Wan Tinn, Zhu, Zhihong, Lukowski, Samuel W., McKinnon, Brett D., McRae, Allan, Yang, Jian, Healey, Martin, Powell, Joseph E., Rogers, Peter A. W., Montgomery, Grant W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065421/
https://www.ncbi.nlm.nih.gov/pubmed/30061686
http://dx.doi.org/10.1038/s41598-018-29462-y
_version_ 1783342864946692096
author Fung, Jenny N.
Mortlock, Sally
Girling, Jane E.
Holdsworth-Carson, Sarah J.
Teh, Wan Tinn
Zhu, Zhihong
Lukowski, Samuel W.
McKinnon, Brett D.
McRae, Allan
Yang, Jian
Healey, Martin
Powell, Joseph E.
Rogers, Peter A. W.
Montgomery, Grant W.
author_facet Fung, Jenny N.
Mortlock, Sally
Girling, Jane E.
Holdsworth-Carson, Sarah J.
Teh, Wan Tinn
Zhu, Zhihong
Lukowski, Samuel W.
McKinnon, Brett D.
McRae, Allan
Yang, Jian
Healey, Martin
Powell, Joseph E.
Rogers, Peter A. W.
Montgomery, Grant W.
author_sort Fung, Jenny N.
collection PubMed
description Gene expression varies markedly across the menstrual cycle and expression levels for many genes are under genetic control. We analyzed gene expression and mapped expression quantitative trait loci (eQTLs) in endometrial tissue samples from 229 women and then analyzed the overlap of endometrial eQTL signals with genomic regions associated with endometriosis and other reproductive traits. We observed a total of 45,923 cis-eQTLs for 417 unique genes and 2,968 trans-eQTLs affecting 82 unique genes. Two eQTLs were located in known risk regions for endometriosis including LINC00339 on chromosome 1 and VEZT on chromosome 12 and there was evidence for eQTLs that may be target genes in genomic regions associated with other reproductive diseases. Dynamic changes in expression of individual genes across cycle include alterations in both mean expression and transcriptional silencing. Significant effects of cycle stage on mean expression levels were observed for (2,427/15,262) probes with detectable expression in at least 90% of samples and for (2,877/9,626) probes expressed in some, but not all samples. Pathway analysis supports similar biological control of both altered expression levels and transcriptional silencing. Taken together, these data identify strong genetic effects on genes with diverse functions in human endometrium and provide a platform for better understanding genetic effects on endometrial-related pathologies.
format Online
Article
Text
id pubmed-6065421
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-60654212018-08-06 Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome Fung, Jenny N. Mortlock, Sally Girling, Jane E. Holdsworth-Carson, Sarah J. Teh, Wan Tinn Zhu, Zhihong Lukowski, Samuel W. McKinnon, Brett D. McRae, Allan Yang, Jian Healey, Martin Powell, Joseph E. Rogers, Peter A. W. Montgomery, Grant W. Sci Rep Article Gene expression varies markedly across the menstrual cycle and expression levels for many genes are under genetic control. We analyzed gene expression and mapped expression quantitative trait loci (eQTLs) in endometrial tissue samples from 229 women and then analyzed the overlap of endometrial eQTL signals with genomic regions associated with endometriosis and other reproductive traits. We observed a total of 45,923 cis-eQTLs for 417 unique genes and 2,968 trans-eQTLs affecting 82 unique genes. Two eQTLs were located in known risk regions for endometriosis including LINC00339 on chromosome 1 and VEZT on chromosome 12 and there was evidence for eQTLs that may be target genes in genomic regions associated with other reproductive diseases. Dynamic changes in expression of individual genes across cycle include alterations in both mean expression and transcriptional silencing. Significant effects of cycle stage on mean expression levels were observed for (2,427/15,262) probes with detectable expression in at least 90% of samples and for (2,877/9,626) probes expressed in some, but not all samples. Pathway analysis supports similar biological control of both altered expression levels and transcriptional silencing. Taken together, these data identify strong genetic effects on genes with diverse functions in human endometrium and provide a platform for better understanding genetic effects on endometrial-related pathologies. Nature Publishing Group UK 2018-07-30 /pmc/articles/PMC6065421/ /pubmed/30061686 http://dx.doi.org/10.1038/s41598-018-29462-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fung, Jenny N.
Mortlock, Sally
Girling, Jane E.
Holdsworth-Carson, Sarah J.
Teh, Wan Tinn
Zhu, Zhihong
Lukowski, Samuel W.
McKinnon, Brett D.
McRae, Allan
Yang, Jian
Healey, Martin
Powell, Joseph E.
Rogers, Peter A. W.
Montgomery, Grant W.
Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome
title Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome
title_full Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome
title_fullStr Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome
title_full_unstemmed Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome
title_short Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome
title_sort genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065421/
https://www.ncbi.nlm.nih.gov/pubmed/30061686
http://dx.doi.org/10.1038/s41598-018-29462-y
work_keys_str_mv AT fungjennyn geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT mortlocksally geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT girlingjanee geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT holdsworthcarsonsarahj geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT tehwantinn geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT zhuzhihong geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT lukowskisamuelw geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT mckinnonbrettd geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT mcraeallan geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT yangjian geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT healeymartin geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT powelljosephe geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT rogerspeteraw geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome
AT montgomerygrantw geneticregulationofdiseaseriskandendometrialgeneexpressionhighlightspotentialtargetgenesforendometriosisandpolycysticovariansyndrome