Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues.
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...
- Autores:
-
Tourancheau, A
Rouleau, M
Guauque Olarte, Sandra Milena
Villeneuve, L
Gilbert, I
Droit, A
Guillemette, C
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2018
- Institución:
- Universidad Cooperativa de Colombia
- Repositorio:
- Repositorio UCC
- Idioma:
- OAI Identifier:
- oai:repository.ucc.edu.co:20.500.12494/41678
- Acceso en línea:
- https://doi.org/10.14349/rlp.2019.v51.n3.1
https://hdl.handle.net/20.500.12494/41678
- Palabra clave:
- glucuronosyltransferase
proteome
transcriptome
drug
glucuronosyltransferase
transcriptome
UGT1A1 enzyme
UGT2A1 protein
human
alternative RNA splicing
Article
carcinogenesis
controlled study
drug clearance
drug metabolism
drug response
female
gene
gene expression profiling
gene expression regulation
genetic variability
human
human tissue
interindividual variability
male
priority journal
RNA sequence
UGT gene
UGT1 gene
UGT2 gene
drug effect
genetics
metabolic clearance rate
metabolism
pharmacogenetic variant
physiology
procedures
tissue distribution
Gene Expression Profiling
Glucuronosyltransferase
Humans
Metabolic Clearance Rate
Pharmaceutical Preparations
Pharmacogenomic Variants
Tissue Distribution
Transcriptome
- Rights
- closedAccess
- License
- http://purl.org/coar/access_right/c_14cb
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Tourancheau, ARouleau, MGuauque Olarte, Sandra MilenaVilleneuve, LGilbert, IDroit, AGuillemette, C2021-12-16T22:15:42Z2021-12-16T22:15:42Z2018https://doi.org/10.14349/rlp.2019.v51.n3.11470269Xhttps://hdl.handle.net/20.500.12494/41678Tourancheau A,Rouleau M,Guauque S,Villeneuve L,Gilbert I,Droit A,Guillemette C. Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. PHARMACOGENOMICS JOURNAL. 2018. 18. (2):p. 251-261. .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 remodeling in favor 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.0000-0003-0336-9682sandra.guauque@campusucc.edu.co261-251Nature Publishing GroupglucuronosyltransferaseproteometranscriptomedrugglucuronosyltransferasetranscriptomeUGT1A1 enzymeUGT2A1 proteinhumanalternative RNA splicingArticlecarcinogenesiscontrolled studydrug clearancedrug metabolismdrug responsefemalegenegene expression profilinggene expression regulationgenetic variabilityhumanhuman tissueinterindividual variabilitymalepriority journalRNA sequenceUGT geneUGT1 geneUGT2 genedrug effectgeneticsmetabolic clearance ratemetabolismpharmacogenetic variantphysiologyprocedurestissue distributionGene Expression ProfilingGlucuronosyltransferaseHumansMetabolic Clearance RatePharmaceutical PreparationsPharmacogenomic VariantsTissue DistributionTranscriptomeQuantitative profiling of the UGT transcriptome in human drug-metabolizing tissues.Artículohttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1http://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articlehttp://purl.org/redcol/resource_type/ARTinfo:eu-repo/semantics/publishedVersionPHARMACOGENOMICS JOURNALinfo:eu-repo/semantics/closedAccesshttp://purl.org/coar/access_right/c_14cbPublication20.500.12494/41678oai:repository.ucc.edu.co:20.500.12494/416782024-08-20 16:21:35.695metadata.onlyhttps://repository.ucc.edu.coRepositorio Institucional Universidad Cooperativa de Colombiabdigital@metabiblioteca.com |
dc.title.spa.fl_str_mv |
Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. |
title |
Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. |
spellingShingle |
Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. glucuronosyltransferase proteome transcriptome drug glucuronosyltransferase transcriptome UGT1A1 enzyme UGT2A1 protein human alternative RNA splicing Article carcinogenesis controlled study drug clearance drug metabolism drug response female gene gene expression profiling gene expression regulation genetic variability human human tissue interindividual variability male priority journal RNA sequence UGT gene UGT1 gene UGT2 gene drug effect genetics metabolic clearance rate metabolism pharmacogenetic variant physiology procedures tissue distribution Gene Expression Profiling Glucuronosyltransferase Humans Metabolic Clearance Rate Pharmaceutical Preparations Pharmacogenomic Variants Tissue Distribution Transcriptome |
title_short |
Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. |
title_full |
Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. |
title_fullStr |
Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. |
title_full_unstemmed |
Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. |
title_sort |
Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. |
dc.creator.fl_str_mv |
Tourancheau, A Rouleau, M Guauque Olarte, Sandra Milena Villeneuve, L Gilbert, I Droit, A Guillemette, C |
dc.contributor.author.none.fl_str_mv |
Tourancheau, A Rouleau, M Guauque Olarte, Sandra Milena Villeneuve, L Gilbert, I Droit, A Guillemette, C |
dc.subject.spa.fl_str_mv |
glucuronosyltransferase proteome transcriptome drug glucuronosyltransferase transcriptome UGT1A1 enzyme UGT2A1 protein human alternative RNA splicing Article carcinogenesis controlled study drug clearance drug metabolism drug response female gene gene expression profiling gene expression regulation genetic variability human human tissue interindividual variability male priority journal RNA sequence UGT gene UGT1 gene UGT2 gene drug effect genetics metabolic clearance rate metabolism pharmacogenetic variant physiology procedures tissue distribution Gene Expression Profiling Glucuronosyltransferase Humans Metabolic Clearance Rate Pharmaceutical Preparations Pharmacogenomic Variants Tissue Distribution Transcriptome |
topic |
glucuronosyltransferase proteome transcriptome drug glucuronosyltransferase transcriptome UGT1A1 enzyme UGT2A1 protein human alternative RNA splicing Article carcinogenesis controlled study drug clearance drug metabolism drug response female gene gene expression profiling gene expression regulation genetic variability human human tissue interindividual variability male priority journal RNA sequence UGT gene UGT1 gene UGT2 gene drug effect genetics metabolic clearance rate metabolism pharmacogenetic variant physiology procedures tissue distribution Gene Expression Profiling Glucuronosyltransferase Humans Metabolic Clearance Rate Pharmaceutical Preparations Pharmacogenomic Variants Tissue Distribution Transcriptome |
description |
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 remodeling in favor 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. |
publishDate |
2018 |
dc.date.issued.none.fl_str_mv |
2018 |
dc.date.accessioned.none.fl_str_mv |
2021-12-16T22:15:42Z |
dc.date.available.none.fl_str_mv |
2021-12-16T22:15:42Z |
dc.type.none.fl_str_mv |
Artículo |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.coar.none.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.coarversion.none.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.driver.none.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.redcol.none.fl_str_mv |
http://purl.org/redcol/resource_type/ART |
dc.type.version.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
http://purl.org/coar/resource_type/c_6501 |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
https://doi.org/10.14349/rlp.2019.v51.n3.1 |
dc.identifier.issn.spa.fl_str_mv |
1470269X |
dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/20.500.12494/41678 |
dc.identifier.bibliographicCitation.spa.fl_str_mv |
Tourancheau A,Rouleau M,Guauque S,Villeneuve L,Gilbert I,Droit A,Guillemette C. Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. PHARMACOGENOMICS JOURNAL. 2018. 18. (2):p. 251-261. . |
url |
https://doi.org/10.14349/rlp.2019.v51.n3.1 https://hdl.handle.net/20.500.12494/41678 |
identifier_str_mv |
1470269X Tourancheau A,Rouleau M,Guauque S,Villeneuve L,Gilbert I,Droit A,Guillemette C. Quantitative profiling of the UGT transcriptome in human drug-metabolizing tissues. PHARMACOGENOMICS JOURNAL. 2018. 18. (2):p. 251-261. . |
dc.relation.ispartofjournal.spa.fl_str_mv |
PHARMACOGENOMICS JOURNAL |
dc.rights.accessrights.none.fl_str_mv |
info:eu-repo/semantics/closedAccess |
dc.rights.coar.none.fl_str_mv |
http://purl.org/coar/access_right/c_14cb |
eu_rights_str_mv |
closedAccess |
rights_invalid_str_mv |
http://purl.org/coar/access_right/c_14cb |
dc.format.extent.spa.fl_str_mv |
261-251 |
dc.publisher.spa.fl_str_mv |
Nature Publishing Group |
institution |
Universidad Cooperativa de Colombia |
repository.name.fl_str_mv |
Repositorio Institucional Universidad Cooperativa de Colombia |
repository.mail.fl_str_mv |
bdigital@metabiblioteca.com |
_version_ |
1814247166165647360 |