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Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors
AIMS/HYPOTHESIS: We aimed to identify microRNAs (miRNAs) under transcriptional control of the HNF1β transcription factor, and investigate whether its effect manifests in serum. METHODS: The Polish cohort (N = 60) consisted of 11 patients with HNF1B-MODY, 17 with HNF1A-MODY, 13 with GCK-MODY, an HbA(...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4901123/ https://www.ncbi.nlm.nih.gov/pubmed/27059371 http://dx.doi.org/10.1007/s00125-016-3945-0 |
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author | Fendler, Wojciech Madzio, Joanna Kozinski, Kamil Patel, Kashyap Janikiewicz, Justyna Szopa, Magdalena Tracz, Adam Borowiec, Maciej Jarosz-Chobot, Przemyslawa Mysliwiec, Malgorzata Szadkowska, Agnieszka Hattersley, Andrew T. Ellard, Sian Malecki, Maciej T. Dobrzyn, Agnieszka Mlynarski, Wojciech |
author_facet | Fendler, Wojciech Madzio, Joanna Kozinski, Kamil Patel, Kashyap Janikiewicz, Justyna Szopa, Magdalena Tracz, Adam Borowiec, Maciej Jarosz-Chobot, Przemyslawa Mysliwiec, Malgorzata Szadkowska, Agnieszka Hattersley, Andrew T. Ellard, Sian Malecki, Maciej T. Dobrzyn, Agnieszka Mlynarski, Wojciech |
author_sort | Fendler, Wojciech |
collection | PubMed |
description | AIMS/HYPOTHESIS: We aimed to identify microRNAs (miRNAs) under transcriptional control of the HNF1β transcription factor, and investigate whether its effect manifests in serum. METHODS: The Polish cohort (N = 60) consisted of 11 patients with HNF1B-MODY, 17 with HNF1A-MODY, 13 with GCK-MODY, an HbA(1c)-matched type 1 diabetic group (n = 9) and ten healthy controls. Replication was performed in 61 clinically-matched British patients mirroring the groups in the Polish cohort. The Polish cohort underwent miRNA serum level profiling with quantitative real-time PCR (qPCR) arrays to identify differentially expressed miRNAs. Validation was performed using qPCR. To determine whether serum content reflects alterations at a cellular level, we quantified miRNA levels in a human hepatocyte cell line (HepG2) with small interfering RNA knockdowns of HNF1α or HNF1β. RESULTS: Significant differences (adjusted p < 0.05) were noted for 11 miRNAs. Five of them differed between HNF1A-MODY and HNF1B-MODY, and, amongst those, four (miR-24, miR-27b, miR-223 and miR-199a) showed HNF1B-MODY-specific expression levels in the replication group. In all four cases the miRNA expression level was lower in HNF1B-MODY than in all other tested groups. Areas under the receiver operating characteristic curves ranged from 0.79 to 0.86, with sensitivity and specificity reaching 91.7% (miR-24) and 82.1% (miR-199a), respectively. The cellular expression pattern of miRNA was consistent with serum levels, as all were significantly higher in HNF1α- than in HNF1β-deficient HepG2 cells. CONCLUSIONS/INTERPRETATION: We have shown that expression of specific miRNAs depends on HNF1β function. The impact of HNF1β deficiency was evidenced at serum level, making HNF1β-dependent miRNAs potentially applicable in the diagnosis of HNF1B-MODY. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00125-016-3945-0) contains peer-reviewed but unedited supplementary material, which is available to authorised users. |
format | Online Article Text |
id | pubmed-4901123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-49011232016-06-27 Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors Fendler, Wojciech Madzio, Joanna Kozinski, Kamil Patel, Kashyap Janikiewicz, Justyna Szopa, Magdalena Tracz, Adam Borowiec, Maciej Jarosz-Chobot, Przemyslawa Mysliwiec, Malgorzata Szadkowska, Agnieszka Hattersley, Andrew T. Ellard, Sian Malecki, Maciej T. Dobrzyn, Agnieszka Mlynarski, Wojciech Diabetologia Article AIMS/HYPOTHESIS: We aimed to identify microRNAs (miRNAs) under transcriptional control of the HNF1β transcription factor, and investigate whether its effect manifests in serum. METHODS: The Polish cohort (N = 60) consisted of 11 patients with HNF1B-MODY, 17 with HNF1A-MODY, 13 with GCK-MODY, an HbA(1c)-matched type 1 diabetic group (n = 9) and ten healthy controls. Replication was performed in 61 clinically-matched British patients mirroring the groups in the Polish cohort. The Polish cohort underwent miRNA serum level profiling with quantitative real-time PCR (qPCR) arrays to identify differentially expressed miRNAs. Validation was performed using qPCR. To determine whether serum content reflects alterations at a cellular level, we quantified miRNA levels in a human hepatocyte cell line (HepG2) with small interfering RNA knockdowns of HNF1α or HNF1β. RESULTS: Significant differences (adjusted p < 0.05) were noted for 11 miRNAs. Five of them differed between HNF1A-MODY and HNF1B-MODY, and, amongst those, four (miR-24, miR-27b, miR-223 and miR-199a) showed HNF1B-MODY-specific expression levels in the replication group. In all four cases the miRNA expression level was lower in HNF1B-MODY than in all other tested groups. Areas under the receiver operating characteristic curves ranged from 0.79 to 0.86, with sensitivity and specificity reaching 91.7% (miR-24) and 82.1% (miR-199a), respectively. The cellular expression pattern of miRNA was consistent with serum levels, as all were significantly higher in HNF1α- than in HNF1β-deficient HepG2 cells. CONCLUSIONS/INTERPRETATION: We have shown that expression of specific miRNAs depends on HNF1β function. The impact of HNF1β deficiency was evidenced at serum level, making HNF1β-dependent miRNAs potentially applicable in the diagnosis of HNF1B-MODY. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00125-016-3945-0) contains peer-reviewed but unedited supplementary material, which is available to authorised users. Springer Berlin Heidelberg 2016-04-08 2016 /pmc/articles/PMC4901123/ /pubmed/27059371 http://dx.doi.org/10.1007/s00125-016-3945-0 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Fendler, Wojciech Madzio, Joanna Kozinski, Kamil Patel, Kashyap Janikiewicz, Justyna Szopa, Magdalena Tracz, Adam Borowiec, Maciej Jarosz-Chobot, Przemyslawa Mysliwiec, Malgorzata Szadkowska, Agnieszka Hattersley, Andrew T. Ellard, Sian Malecki, Maciej T. Dobrzyn, Agnieszka Mlynarski, Wojciech Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors |
title | Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors |
title_full | Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors |
title_fullStr | Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors |
title_full_unstemmed | Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors |
title_short | Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors |
title_sort | differential regulation of serum microrna expression by hnf1β and hnf1α transcription factors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4901123/ https://www.ncbi.nlm.nih.gov/pubmed/27059371 http://dx.doi.org/10.1007/s00125-016-3945-0 |
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