Literature DB >> 29117547

A Prostate Cancer Risk Element Functions as a Repressive Loop that Regulates HOXA13.

Zhifei Luo1, Suhn Kyong Rhie1, Fides D Lay1, Peggy J Farnham2.   

Abstract

Prostate cancer (PCa) is the leading cancer among men in the United States, with genetic factors contributing to ∼42% of the susceptibility to PCa. We analyzed a PCa risk region located at 7p15.2 to gain insight into the mechanisms by which this noncoding region may affect gene regulation and contribute to PCa risk. We performed Hi-C analysis and demonstrated that this region has long-range interactions with the HOXA locus, located ∼873 kb away. Using the CRISPR/Cas9 system, we deleted a 4-kb region encompassing several PCa risk-associated SNPs and performed RNA-seq to investigate transcriptomic changes in prostate cells lacking the regulatory element. Our results suggest that the risk element affects the expression of HOXA13 and HOTTIP, but not other genes in the HOXA locus, via a repressive loop. Forced expression of HOXA13 was performed to gain further insight into the mechanisms by which this risk element affects PCa risk.
Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CRISPR; GWAS; HOX genes; Hi-C; chromatin structure; transcriptional regulation

Mesh:

Substances:

Year:  2017        PMID: 29117547      PMCID: PMC5726543          DOI: 10.1016/j.celrep.2017.10.048

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  41 in total

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7.  Evaluation of GWAS-Identified Genetic Variants for Gastric Cancer Survival.

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10.  CRISPR-mediated deletion of prostate cancer risk-associated CTCF loop anchors identifies repressive chromatin loops.

Authors:  Yu Guo; Andrew A Perez; Dennis J Hazelett; Gerhard A Coetzee; Suhn Kyong Rhie; Peggy J Farnham
Journal:  Genome Biol       Date:  2018-10-08       Impact factor: 13.583

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