Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148

Publication date

2020-04-28T16:34:16Z

2020-04-28T16:34:16Z

2017-05-02

2020-04-28T16:34:16Z

Abstract

Genome wide association studies (GWAS) have mapped multiple independent cancer susceptibility loci to chr5p15.33. Here, we show that fine-mapping of pancreatic and testicular cancer GWAS within one of these loci (Region 2 in CLPTM1L) focuses the signal to nine highly correlated SNPs. Of these, rs36115365-C associated with increased pancreatic and testicular but decreased lung cancer and melanoma risk, and exhibited preferred protein-binding and enhanced regulatory activity. Transcriptional gene silencing of this regulatory element repressed TERT expression in an allele-specific manner. Proteomic analysis identifies allele-preferred binding of Zinc finger protein 148 (ZNF148) to rs36115365-C, further supported by binding of purified recombinant ZNF148. Knockdown of ZNF148 results in reduced TERT expression, telomerase activity and telomere length. Our results indicate that the association with chr5p15.33-Region 2 may be explained by rs36115365, a variant influencing TERT expression via ZNF148 in a manner consistent with elevated TERT in carriers of the C allele.

Document Type

Article


Published version

Language

English

Publisher

Nature Publishing Group

Related items

Reproducció del document publicat a: https://doi.org/10.1038/ncomms15034

Nature Communications, 2018, vol. 8, p. 15034

https://doi.org/10.1038/ncomms15034

info:eu-repo/grantAgreement/EC/FP7/607142/EU//DEVCOM

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cc-by (c) Fang, Jun et al., 2018

http://creativecommons.org/licenses/by/3.0/es