Quantitative profiling of the UGT transcriptome in human drug metabolizing tissues

Authors: Tourancheau, AlanRouleau, MichèleGuauque-Olarte, SandraVilleneuve, LyneGilbert, IsabelleDroit, ArnaudGuillemette, Chantal
Abstract: Alternative splicing as a mean to control gene expression and diversify function is suspected to considerably influence drug response and clearance. We report the quantitative expression profiles of the human UGT genes including alternatively spliced variants not previously annotated established by deep RNA-sequencing in tissues of pharmacological importance. We reveal a comprehensive quantification of the alternative UGT transcriptome that differ across tissues and among individuals. Alternative transcripts that comprise novel in-frame sequences associated or not with truncations of the 5’ and/or 3’ termini, significantly contribute to the total expression levels of each UGT1 and UGT2 gene averaging 21% in normal tissues, with expression of UGT2 variants surpassing those of UGT1. Quantitative data expose preferential tissue expression patterns and remodelling in favour of alternative variants upon tumorigenesis. These complex alternative splicing programs have the strong potential to contribute to interindividual variability in drug metabolism in addition to diversify the UGT proteome.
Document Type: Article de recherche
Issue Date: 25 April 2017
Open Access Date: 25 October 2017
Document version: AM
Permalink: http://hdl.handle.net/20.500.11794/13068
This document was published in: The Pharmacogenomics Journal (2017)
https://doi.org/10.1038/tpj.2017.5
Nature Publishing Group.
Alternative version: 10.1038/tpj.2017.5
28440341
Collection:Articles publiés dans des revues avec comité de lecture

Files in this item:
SizeFormat 
Accepted_Tourancheau_2017.pdf
1.03 MBAdobe PDF    Request a copy
All documents in CorpusUL are protected by Copyright Act of Canada.