A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.

Genetic mapping studies have identified multiple cancer susceptibility regions at chromosome 8q24, upstream of the MYC oncogene. MYC has been widely presumed as the regulated target gene, but definitive evidence functionally linking these cancer regions with MYC has been difficult to obtain. Here we...

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Main Authors: Kerstin B Meyer, Ana-Teresa Maia, Martin O'Reilly, Maya Ghoussaini, Radhika Prathalingam, Patricia Porter-Gill, Stefan Ambs, Ludmila Prokunina-Olsson, Jason Carroll, Bruce A J Ponder
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-07-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3140991?pdf=render
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spelling doaj-6886a64a922d47dca3e6cca927106fb32020-11-25T01:23:33ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042011-07-0177e100216510.1371/journal.pgen.1002165A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.Kerstin B MeyerAna-Teresa MaiaMartin O'ReillyMaya GhoussainiRadhika PrathalingamPatricia Porter-GillStefan AmbsLudmila Prokunina-OlssonJason CarrollBruce A J PonderGenetic mapping studies have identified multiple cancer susceptibility regions at chromosome 8q24, upstream of the MYC oncogene. MYC has been widely presumed as the regulated target gene, but definitive evidence functionally linking these cancer regions with MYC has been difficult to obtain. Here we examined candidate functional variants of a haplotype block at 8q24 encompassing the two independent risk alleles for prostate and breast cancer, rs620861 and rs13281615. We used the mapping of DNase I hypersensitive sites as a tool to prioritise regions for further functional analysis. This approach identified rs378854, which is in complete linkage disequilibrium (LD) with rs620861, as a novel functional prostate cancer-specific genetic variant. We demonstrate that the risk allele (G) of rs378854 reduces binding of the transcription factor YY1 in vitro. This factor is known to repress global transcription in prostate cancer and is a candidate tumour suppressor. Additional experiments showed that the YY1 binding site is occupied in vivo in prostate cancer, but not breast cancer cells, consistent with the observed cancer-specific effects of this single nucleotide polymorphism (SNP). Using chromatin conformation capture (3C) experiments, we found that the region surrounding rs378854 interacts with the MYC and PVT1 promoters. Moreover, expression of the PVT1 oncogene in normal prostate tissue increased with the presence of the risk allele of rs378854, while expression of MYC was not affected. In conclusion, we identified a new functional prostate cancer risk variant at the 8q24 locus, rs378854 allele G, that reduces binding of the YY1 protein and is associated with increased expression of PVT1 located 0.5 Mb downstream.http://europepmc.org/articles/PMC3140991?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kerstin B Meyer
Ana-Teresa Maia
Martin O'Reilly
Maya Ghoussaini
Radhika Prathalingam
Patricia Porter-Gill
Stefan Ambs
Ludmila Prokunina-Olsson
Jason Carroll
Bruce A J Ponder
spellingShingle Kerstin B Meyer
Ana-Teresa Maia
Martin O'Reilly
Maya Ghoussaini
Radhika Prathalingam
Patricia Porter-Gill
Stefan Ambs
Ludmila Prokunina-Olsson
Jason Carroll
Bruce A J Ponder
A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.
PLoS Genetics
author_facet Kerstin B Meyer
Ana-Teresa Maia
Martin O'Reilly
Maya Ghoussaini
Radhika Prathalingam
Patricia Porter-Gill
Stefan Ambs
Ludmila Prokunina-Olsson
Jason Carroll
Bruce A J Ponder
author_sort Kerstin B Meyer
title A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.
title_short A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.
title_full A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.
title_fullStr A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.
title_full_unstemmed A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.
title_sort functional variant at a prostate cancer predisposition locus at 8q24 is associated with pvt1 expression.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2011-07-01
description Genetic mapping studies have identified multiple cancer susceptibility regions at chromosome 8q24, upstream of the MYC oncogene. MYC has been widely presumed as the regulated target gene, but definitive evidence functionally linking these cancer regions with MYC has been difficult to obtain. Here we examined candidate functional variants of a haplotype block at 8q24 encompassing the two independent risk alleles for prostate and breast cancer, rs620861 and rs13281615. We used the mapping of DNase I hypersensitive sites as a tool to prioritise regions for further functional analysis. This approach identified rs378854, which is in complete linkage disequilibrium (LD) with rs620861, as a novel functional prostate cancer-specific genetic variant. We demonstrate that the risk allele (G) of rs378854 reduces binding of the transcription factor YY1 in vitro. This factor is known to repress global transcription in prostate cancer and is a candidate tumour suppressor. Additional experiments showed that the YY1 binding site is occupied in vivo in prostate cancer, but not breast cancer cells, consistent with the observed cancer-specific effects of this single nucleotide polymorphism (SNP). Using chromatin conformation capture (3C) experiments, we found that the region surrounding rs378854 interacts with the MYC and PVT1 promoters. Moreover, expression of the PVT1 oncogene in normal prostate tissue increased with the presence of the risk allele of rs378854, while expression of MYC was not affected. In conclusion, we identified a new functional prostate cancer risk variant at the 8q24 locus, rs378854 allele G, that reduces binding of the YY1 protein and is associated with increased expression of PVT1 located 0.5 Mb downstream.
url http://europepmc.org/articles/PMC3140991?pdf=render
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