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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(...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
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.
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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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