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A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer

Genetic variation at the 8q24 locus is linked with the greater susceptibility to prostate cancer in men of African ancestry. One such African ancestry specific rare variant, rs72725854 (A>G/T) (~6% allele frequency) has been associated with a ~2-fold increase in prostate cancer risk. However, the...

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Autores principales: Walavalkar, Kaivalya, Saravanan, Bharath, Singh, Anurag Kumar, Jayani, Ranveer Singh, Nair, Ashwin, Farooq, Umer, Islam, Zubairul, Soota, Deepanshu, Mann, Rajat, Shivaprasad, Padubidri V., Freedman, Matthew L., Sabarinathan, Radhakrishnan, Haiman, Christopher A., Notani, Dimple
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368061/
https://www.ncbi.nlm.nih.gov/pubmed/32680982
http://dx.doi.org/10.1038/s41467-020-17325-y
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author Walavalkar, Kaivalya
Saravanan, Bharath
Singh, Anurag Kumar
Jayani, Ranveer Singh
Nair, Ashwin
Farooq, Umer
Islam, Zubairul
Soota, Deepanshu
Mann, Rajat
Shivaprasad, Padubidri V.
Freedman, Matthew L.
Sabarinathan, Radhakrishnan
Haiman, Christopher A.
Notani, Dimple
author_facet Walavalkar, Kaivalya
Saravanan, Bharath
Singh, Anurag Kumar
Jayani, Ranveer Singh
Nair, Ashwin
Farooq, Umer
Islam, Zubairul
Soota, Deepanshu
Mann, Rajat
Shivaprasad, Padubidri V.
Freedman, Matthew L.
Sabarinathan, Radhakrishnan
Haiman, Christopher A.
Notani, Dimple
author_sort Walavalkar, Kaivalya
collection PubMed
description Genetic variation at the 8q24 locus is linked with the greater susceptibility to prostate cancer in men of African ancestry. One such African ancestry specific rare variant, rs72725854 (A>G/T) (~6% allele frequency) has been associated with a ~2-fold increase in prostate cancer risk. However, the functional relevance of this variant is unknown. Here we show that the variant rs72725854 is present in a prostate cancer-specific enhancer at 8q24 locus. Chromatin-conformation capture and dCas9 mediated enhancer blocking establish a direct regulatory link between this enhancer and lncRNAs PCAT1, PRNCR1 and PVT1. The risk allele (‘T’) is associated with higher expression of PCAT1, PVT1 and c-myc in prostate tumors. Further, enhancer with the risk allele gains response to androgen stimulation by recruiting the transcription factor SPDEF whereas, non-risk alleles remain non-responsive. Elevated expression of these lncRNAs and c-myc in risk allele carriers may explain their greater susceptibility to prostate cancer.
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spelling pubmed-73680612020-07-21 A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer Walavalkar, Kaivalya Saravanan, Bharath Singh, Anurag Kumar Jayani, Ranveer Singh Nair, Ashwin Farooq, Umer Islam, Zubairul Soota, Deepanshu Mann, Rajat Shivaprasad, Padubidri V. Freedman, Matthew L. Sabarinathan, Radhakrishnan Haiman, Christopher A. Notani, Dimple Nat Commun Article Genetic variation at the 8q24 locus is linked with the greater susceptibility to prostate cancer in men of African ancestry. One such African ancestry specific rare variant, rs72725854 (A>G/T) (~6% allele frequency) has been associated with a ~2-fold increase in prostate cancer risk. However, the functional relevance of this variant is unknown. Here we show that the variant rs72725854 is present in a prostate cancer-specific enhancer at 8q24 locus. Chromatin-conformation capture and dCas9 mediated enhancer blocking establish a direct regulatory link between this enhancer and lncRNAs PCAT1, PRNCR1 and PVT1. The risk allele (‘T’) is associated with higher expression of PCAT1, PVT1 and c-myc in prostate tumors. Further, enhancer with the risk allele gains response to androgen stimulation by recruiting the transcription factor SPDEF whereas, non-risk alleles remain non-responsive. Elevated expression of these lncRNAs and c-myc in risk allele carriers may explain their greater susceptibility to prostate cancer. Nature Publishing Group UK 2020-07-17 /pmc/articles/PMC7368061/ /pubmed/32680982 http://dx.doi.org/10.1038/s41467-020-17325-y Text en © The Author(s) 2020 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
Walavalkar, Kaivalya
Saravanan, Bharath
Singh, Anurag Kumar
Jayani, Ranveer Singh
Nair, Ashwin
Farooq, Umer
Islam, Zubairul
Soota, Deepanshu
Mann, Rajat
Shivaprasad, Padubidri V.
Freedman, Matthew L.
Sabarinathan, Radhakrishnan
Haiman, Christopher A.
Notani, Dimple
A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer
title A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer
title_full A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer
title_fullStr A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer
title_full_unstemmed A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer
title_short A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer
title_sort rare variant of african ancestry activates 8q24 lncrna hub by modulating cancer associated enhancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368061/
https://www.ncbi.nlm.nih.gov/pubmed/32680982
http://dx.doi.org/10.1038/s41467-020-17325-y
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