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Regulation of Pancreatic microRNA-7 Expression

Genome-encoded microRNAs (miRNAs) provide a posttranscriptional regulatory layer, which is important for pancreas development. Differentiation of endocrine cells is controlled by a network of pancreatic transcription factors including Ngn3 and NeuroD/Beta2. However, how specific miRNAs are intertwin...

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Autores principales: Kredo-Russo, Sharon, Ness, Avital, Mandelbaum, Amitai D., Walker, Michael D., Hornstein, Eran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362837/
https://www.ncbi.nlm.nih.gov/pubmed/22675342
http://dx.doi.org/10.1155/2012/695214
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author Kredo-Russo, Sharon
Ness, Avital
Mandelbaum, Amitai D.
Walker, Michael D.
Hornstein, Eran
author_facet Kredo-Russo, Sharon
Ness, Avital
Mandelbaum, Amitai D.
Walker, Michael D.
Hornstein, Eran
author_sort Kredo-Russo, Sharon
collection PubMed
description Genome-encoded microRNAs (miRNAs) provide a posttranscriptional regulatory layer, which is important for pancreas development. Differentiation of endocrine cells is controlled by a network of pancreatic transcription factors including Ngn3 and NeuroD/Beta2. However, how specific miRNAs are intertwined into this transcriptional network is not well understood. Here, we characterize the regulation of microRNA-7 (miR-7) by endocrine-specific transcription factors. Our data reveal that three independent miR-7 genes are coexpressed in the pancreas. We have identified conserved blocks upstream of pre-miR-7a-2 and pre-miR-7b and demonstrated by functional assays that they possess promoter activity, which is increased by the expression of NeuroD/Beta2. These data suggest that the endocrine specificity of miR-7 expression is governed by transcriptional mechanisms and involves members of the pancreatic endocrine network of transcription factors.
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spelling pubmed-33628372012-06-06 Regulation of Pancreatic microRNA-7 Expression Kredo-Russo, Sharon Ness, Avital Mandelbaum, Amitai D. Walker, Michael D. Hornstein, Eran Exp Diabetes Res Research Article Genome-encoded microRNAs (miRNAs) provide a posttranscriptional regulatory layer, which is important for pancreas development. Differentiation of endocrine cells is controlled by a network of pancreatic transcription factors including Ngn3 and NeuroD/Beta2. However, how specific miRNAs are intertwined into this transcriptional network is not well understood. Here, we characterize the regulation of microRNA-7 (miR-7) by endocrine-specific transcription factors. Our data reveal that three independent miR-7 genes are coexpressed in the pancreas. We have identified conserved blocks upstream of pre-miR-7a-2 and pre-miR-7b and demonstrated by functional assays that they possess promoter activity, which is increased by the expression of NeuroD/Beta2. These data suggest that the endocrine specificity of miR-7 expression is governed by transcriptional mechanisms and involves members of the pancreatic endocrine network of transcription factors. Hindawi Publishing Corporation 2012 2012-05-17 /pmc/articles/PMC3362837/ /pubmed/22675342 http://dx.doi.org/10.1155/2012/695214 Text en Copyright © 2012 Sharon Kredo-Russo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kredo-Russo, Sharon
Ness, Avital
Mandelbaum, Amitai D.
Walker, Michael D.
Hornstein, Eran
Regulation of Pancreatic microRNA-7 Expression
title Regulation of Pancreatic microRNA-7 Expression
title_full Regulation of Pancreatic microRNA-7 Expression
title_fullStr Regulation of Pancreatic microRNA-7 Expression
title_full_unstemmed Regulation of Pancreatic microRNA-7 Expression
title_short Regulation of Pancreatic microRNA-7 Expression
title_sort regulation of pancreatic microrna-7 expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362837/
https://www.ncbi.nlm.nih.gov/pubmed/22675342
http://dx.doi.org/10.1155/2012/695214
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