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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...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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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. |
format | Text |
id | pubmed-2717370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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