Matches in SemOpenAlex for { <https://semopenalex.org/work/W2034609222> ?p ?o ?g. }
- W2034609222 endingPage "e48622" @default.
- W2034609222 startingPage "e48622" @default.
- W2034609222 abstract "MicroRNAs (miRNAs) are small RNAs responsible for the post-transcriptional regulation of a variety of human genes. To date, their involvement in the regulation of CBR1 is unknown. This study reports for the first time the identification of microRNA-574-5p (hsa-miR-574-5p) and microRNA-921 (hsa-miR-921) as two miRNAs capable of interacting with the 3'-untranslated region (3'-UTR) of the CBR1 gene and downregulating CBR1 expression. Furthermore, we demonstrate that a common single-nucleotide polymorphism (SNP) in the CBR1 3'-UTR (rs9024, CBR1 1096G>A) differentially impacts the regulation of CBR1 by hsa-miR-574-5p and hsa-miR-921 dependent on genotype. First, four candidate miRNAs were selected based on bioinformatic analyses, and were tested in Chinese hamster ovary (CHO) cells transfected with CBR1 3'-UTR constructs harboring either the G or A allele for rs9024. We found that hsa-miR-574-5p and hsa-miR-921 significantly decreased luciferase activity in CHO cells transfected with the CBR1 3'-UTR construct carrying the major rs9024 G allele by 35% and 46%, respectively. The influence of these miRNAs was different in cells transfected with a CBR1 3'-UTR construct containing the minor rs9024 A allele in that only hsa-miR-574-5p had a demonstrable effect (i.e., 52% decrease in lucifersase activity). To further determine the functional effects of miRNA-mediated regulation of polymorphic CBR1, we assessed CBR1 protein expression and CBR1 enzymatic activity for the prototypical substrate menadione in human lymphoblastoid cell lines with distinct rs9024 genotypes. We found that hsa-miR-574-5p and hsa-miR-921 significantly decreased CBR1 protein (48% and 40%, respectively) and CBR1 menadione activity (54% and 18%, respectively) in lymphoblastoid cells homozygous for the major rs9024 G allele. In contrast, only hsa-miR-574-5p decreased CBR1 protein and CBR1 activity in cells homozygous for the minor rs9024 A allele, and did so by 49% and 56%, respectively. These results suggest that regulation of human CBR1 expression by hsa-miR-574-5p and hsa-miR-921 depends upon rs9024 genotype status." @default.
- W2034609222 created "2016-06-24" @default.
- W2034609222 creator A5004637134 @default.
- W2034609222 creator A5012031316 @default.
- W2034609222 creator A5085944662 @default.
- W2034609222 date "2012-11-01" @default.
- W2034609222 modified "2023-10-16" @default.
- W2034609222 title "MicroRNAs Differentially Regulate Carbonyl Reductase 1 (CBR1) Gene Expression Dependent on the Allele Status of the Common Polymorphic Variant rs9024" @default.
- W2034609222 cites W144423133 @default.
- W2034609222 cites W1985825541 @default.
- W2034609222 cites W1990535142 @default.
- W2034609222 cites W2014946489 @default.
- W2034609222 cites W2014981212 @default.
- W2034609222 cites W2026570544 @default.
- W2034609222 cites W2044043408 @default.
- W2034609222 cites W2053291556 @default.
- W2034609222 cites W2060181803 @default.
- W2034609222 cites W2070571588 @default.
- W2034609222 cites W2083381199 @default.
- W2034609222 cites W2086809547 @default.
- W2034609222 cites W2089856956 @default.
- W2034609222 cites W2090633960 @default.
- W2034609222 cites W2106885128 @default.
- W2034609222 cites W2112785261 @default.
- W2034609222 cites W2115440941 @default.
- W2034609222 cites W2117391818 @default.
- W2034609222 cites W2121153171 @default.
- W2034609222 cites W2124427987 @default.
- W2034609222 cites W2147809056 @default.
- W2034609222 cites W2149785901 @default.
- W2034609222 cites W2150699891 @default.
- W2034609222 cites W2152868870 @default.
- W2034609222 cites W2154085311 @default.
- W2034609222 cites W2156133650 @default.
- W2034609222 cites W2156925439 @default.
- W2034609222 cites W24203564 @default.
- W2034609222 cites W4211182860 @default.
- W2034609222 doi "https://doi.org/10.1371/journal.pone.0048622" @default.
- W2034609222 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3486798" @default.
- W2034609222 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23133646" @default.
- W2034609222 hasPublicationYear "2012" @default.
- W2034609222 type Work @default.
- W2034609222 sameAs 2034609222 @default.
- W2034609222 citedByCount "17" @default.
- W2034609222 countsByYear W20346092222012 @default.
- W2034609222 countsByYear W20346092222013 @default.
- W2034609222 countsByYear W20346092222014 @default.
- W2034609222 countsByYear W20346092222015 @default.
- W2034609222 countsByYear W20346092222016 @default.
- W2034609222 countsByYear W20346092222017 @default.
- W2034609222 countsByYear W20346092222018 @default.
- W2034609222 countsByYear W20346092222019 @default.
- W2034609222 countsByYear W20346092222021 @default.
- W2034609222 countsByYear W20346092222022 @default.
- W2034609222 crossrefType "journal-article" @default.
- W2034609222 hasAuthorship W2034609222A5004637134 @default.
- W2034609222 hasAuthorship W2034609222A5012031316 @default.
- W2034609222 hasAuthorship W2034609222A5085944662 @default.
- W2034609222 hasBestOaLocation W20346092221 @default.
- W2034609222 hasConcept C104317684 @default.
- W2034609222 hasConcept C105580179 @default.
- W2034609222 hasConcept C111335760 @default.
- W2034609222 hasConcept C145059251 @default.
- W2034609222 hasConcept C150194340 @default.
- W2034609222 hasConcept C153911025 @default.
- W2034609222 hasConcept C165864922 @default.
- W2034609222 hasConcept C175656101 @default.
- W2034609222 hasConcept C22667442 @default.
- W2034609222 hasConcept C54009773 @default.
- W2034609222 hasConcept C54355233 @default.
- W2034609222 hasConcept C81885089 @default.
- W2034609222 hasConcept C86803240 @default.
- W2034609222 hasConcept C89604277 @default.
- W2034609222 hasConceptScore W2034609222C104317684 @default.
- W2034609222 hasConceptScore W2034609222C105580179 @default.
- W2034609222 hasConceptScore W2034609222C111335760 @default.
- W2034609222 hasConceptScore W2034609222C145059251 @default.
- W2034609222 hasConceptScore W2034609222C150194340 @default.
- W2034609222 hasConceptScore W2034609222C153911025 @default.
- W2034609222 hasConceptScore W2034609222C165864922 @default.
- W2034609222 hasConceptScore W2034609222C175656101 @default.
- W2034609222 hasConceptScore W2034609222C22667442 @default.
- W2034609222 hasConceptScore W2034609222C54009773 @default.
- W2034609222 hasConceptScore W2034609222C54355233 @default.
- W2034609222 hasConceptScore W2034609222C81885089 @default.
- W2034609222 hasConceptScore W2034609222C86803240 @default.
- W2034609222 hasConceptScore W2034609222C89604277 @default.
- W2034609222 hasIssue "11" @default.
- W2034609222 hasLocation W20346092221 @default.
- W2034609222 hasLocation W20346092222 @default.
- W2034609222 hasLocation W20346092223 @default.
- W2034609222 hasLocation W20346092224 @default.
- W2034609222 hasLocation W20346092225 @default.
- W2034609222 hasOpenAccess W2034609222 @default.
- W2034609222 hasPrimaryLocation W20346092221 @default.
- W2034609222 hasRelatedWork W193469943 @default.
- W2034609222 hasRelatedWork W1964500896 @default.
- W2034609222 hasRelatedWork W2055765836 @default.