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Comprehensive quantitative analysis of alternative splicing variants reveals the HNF1B mRNA splicing pattern in various tumour and non-tumour tissues
J. Hojny, R. Michalkova, E. Krkavcova, QH. Bui, M. Bartu, K. Nemejcova, M. Kalousova, P. Kleiblova, P. Dundr, I. Struzinska
Language English Country Great Britain
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
Grant support
64165
Ministerstvo Zdravotnictví Ceské Republiky
204065
Univerzita Karlova v Praze
CZ.02.1.01/0.0/0.0/18_046/ 0015959
European Regional Development Fund
NLK
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- MeSH
- Alternative Splicing * MeSH
- Hepatocyte Nuclear Factor 1-beta genetics metabolism MeSH
- Humans MeSH
- RNA, Messenger genetics metabolism MeSH
- Biomarkers, Tumor genetics metabolism MeSH
- Neoplasms genetics metabolism MeSH
- Polymerase Chain Reaction MeSH
- Protein Isoforms MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Retrospective Studies MeSH
- RNA, Neoplasm genetics metabolism MeSH
- High-Throughput Nucleotide Sequencing MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
Hepatocyte nuclear factor-1-beta (HNF1B) is a transcription factor and putative biomarker of solid tumours. Recently, we have revealed a variety of HNF1B mRNA alternative splicing variants (ASVs) with unknown, but potentially regulatory, functions. The aim of our work was to quantify the most common variants and compare their expression in tumour and non-tumour tissues of the large intestine, prostate, and kidney. The HNF1B mRNA variants 3p, Δ7, Δ7-8, and Δ8 were expressed across all the analysed tissues in 28.2-33.5%, 1.5-2%, 0.8-1.7%, and 2.3-6.9% of overall HNF1B mRNA expression, respectively, and occurred individually or in combination. The quantitative changes of ASVs between tumour and non-tumour tissue were observed for the large intestine (3p, Δ7-8), prostate (3p), and kidney samples (Δ7). Decreased expression of the overall HNF1B mRNA in the large intestine and prostate cancer samples compared with the corresponding non-tumour samples was observed (p = 0.019 and p = 0.047, respectively). The decreased mRNA expression correlated with decreased protein expression in large intestine carcinomas (p < 0.001). The qualitative and quantitative pattern of the ASVs studied by droplet digital PCR was confirmed by next-generation sequencing, which suggests the significance of the NGS approach for further massive evaluation of the splicing patterns in a variety of genes.
References provided by Crossref.org
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