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Functional Enhancers at the Gene-Poor 8q24 Cancer-Linked Locus

Multiple discrete regions at 8q24 were recently shown to contain alleles that predispose to many cancers including prostate, breast, and colon. These regions are far from any annotated gene and their biological activities have been unknown. Here we profiled a 5-megabase chromatin segment encompassin...

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Autores principales: Jia, Li, Landan, Gilad, Pomerantz, Mark, Jaschek, Rami, Herman, Paula, Reich, David, Yan, Chunli, Khalid, Omar, Kantoff, Phil, Oh, William, Manak, J. Robert, Berman, Benjamin P., Henderson, Brian E., Frenkel, Baruch, Haiman, Christopher A., Freedman, Matthew, Tanay, Amos, Coetzee, Gerhard A.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2717370/
https://www.ncbi.nlm.nih.gov/pubmed/19680443
http://dx.doi.org/10.1371/journal.pgen.1000597
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author Jia, Li
Landan, Gilad
Pomerantz, Mark
Jaschek, Rami
Herman, Paula
Reich, David
Yan, Chunli
Khalid, Omar
Kantoff, Phil
Oh, William
Manak, J. Robert
Berman, Benjamin P.
Henderson, Brian E.
Frenkel, Baruch
Haiman, Christopher A.
Freedman, Matthew
Tanay, Amos
Coetzee, Gerhard A.
author_facet Jia, Li
Landan, Gilad
Pomerantz, Mark
Jaschek, Rami
Herman, Paula
Reich, David
Yan, Chunli
Khalid, Omar
Kantoff, Phil
Oh, William
Manak, J. Robert
Berman, Benjamin P.
Henderson, Brian E.
Frenkel, Baruch
Haiman, Christopher A.
Freedman, Matthew
Tanay, Amos
Coetzee, Gerhard A.
author_sort Jia, Li
collection PubMed
description Multiple discrete regions at 8q24 were recently shown to contain alleles that predispose to many cancers including prostate, breast, and colon. These regions are far from any annotated gene and their biological activities have been unknown. Here we profiled a 5-megabase chromatin segment encompassing all the risk regions for RNA expression, histone modifications, and locations occupied by RNA polymerase II and androgen receptor (AR). This led to the identification of several transcriptional enhancers, which were verified using reporter assays. Two enhancers in one risk region were occupied by AR and responded to androgen treatment; one contained a single nucleotide polymorphism (rs11986220) that resides within a FoxA1 binding site, with the prostate cancer risk allele facilitating both stronger FoxA1 binding and stronger androgen responsiveness. The study reported here exemplifies an approach that may be applied to any risk-associated allele in non-protein coding regions as it emerges from genome-wide association studies to better understand the genetic predisposition of complex diseases.
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spelling pubmed-27173702009-08-14 Functional Enhancers at the Gene-Poor 8q24 Cancer-Linked Locus Jia, Li Landan, Gilad Pomerantz, Mark Jaschek, Rami Herman, Paula Reich, David Yan, Chunli Khalid, Omar Kantoff, Phil Oh, William Manak, J. Robert Berman, Benjamin P. Henderson, Brian E. Frenkel, Baruch Haiman, Christopher A. Freedman, Matthew Tanay, Amos Coetzee, Gerhard A. PLoS Genet Research Article Multiple discrete regions at 8q24 were recently shown to contain alleles that predispose to many cancers including prostate, breast, and colon. These regions are far from any annotated gene and their biological activities have been unknown. Here we profiled a 5-megabase chromatin segment encompassing all the risk regions for RNA expression, histone modifications, and locations occupied by RNA polymerase II and androgen receptor (AR). This led to the identification of several transcriptional enhancers, which were verified using reporter assays. Two enhancers in one risk region were occupied by AR and responded to androgen treatment; one contained a single nucleotide polymorphism (rs11986220) that resides within a FoxA1 binding site, with the prostate cancer risk allele facilitating both stronger FoxA1 binding and stronger androgen responsiveness. The study reported here exemplifies an approach that may be applied to any risk-associated allele in non-protein coding regions as it emerges from genome-wide association studies to better understand the genetic predisposition of complex diseases. Public Library of Science 2009-08-14 /pmc/articles/PMC2717370/ /pubmed/19680443 http://dx.doi.org/10.1371/journal.pgen.1000597 Text en Jia et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jia, Li
Landan, Gilad
Pomerantz, Mark
Jaschek, Rami
Herman, Paula
Reich, David
Yan, Chunli
Khalid, Omar
Kantoff, Phil
Oh, William
Manak, J. Robert
Berman, Benjamin P.
Henderson, Brian E.
Frenkel, Baruch
Haiman, Christopher A.
Freedman, Matthew
Tanay, Amos
Coetzee, Gerhard A.
Functional Enhancers at the Gene-Poor 8q24 Cancer-Linked Locus
title Functional Enhancers at the Gene-Poor 8q24 Cancer-Linked Locus
title_full Functional Enhancers at the Gene-Poor 8q24 Cancer-Linked Locus
title_fullStr Functional Enhancers at the Gene-Poor 8q24 Cancer-Linked Locus
title_full_unstemmed Functional Enhancers at the Gene-Poor 8q24 Cancer-Linked Locus
title_short Functional Enhancers at the Gene-Poor 8q24 Cancer-Linked Locus
title_sort functional enhancers at the gene-poor 8q24 cancer-linked locus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2717370/
https://www.ncbi.nlm.nih.gov/pubmed/19680443
http://dx.doi.org/10.1371/journal.pgen.1000597
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