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Identification and Characterization of Circular Intronic RNAs Derived from Insulin Gene
Circular RNAs (circRNAs) are a large family of noncoding RNAs that have emerged as novel regulators of gene expression. However, little is known about the function of circRNAs in pancreatic β-cells. Here, transcriptomic analysis of mice pancreatic islet RNA-sequencing data identified 77 differential...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352490/ https://www.ncbi.nlm.nih.gov/pubmed/32560282 http://dx.doi.org/10.3390/ijms21124302 |
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author | Das, Debojyoti Das, Aniruddha Sahu, Mousumi Mishra, Smruti Sambhav Khan, Shaheerah Bejugam, Pruthvi R. Rout, Pranita K. Das, Arundhati Bano, Shehnaz Mishra, Gyan Prakash Raghav, Sunil K. Dixit, Anshuman Panda, Amaresh C. |
author_facet | Das, Debojyoti Das, Aniruddha Sahu, Mousumi Mishra, Smruti Sambhav Khan, Shaheerah Bejugam, Pruthvi R. Rout, Pranita K. Das, Arundhati Bano, Shehnaz Mishra, Gyan Prakash Raghav, Sunil K. Dixit, Anshuman Panda, Amaresh C. |
author_sort | Das, Debojyoti |
collection | PubMed |
description | Circular RNAs (circRNAs) are a large family of noncoding RNAs that have emerged as novel regulators of gene expression. However, little is known about the function of circRNAs in pancreatic β-cells. Here, transcriptomic analysis of mice pancreatic islet RNA-sequencing data identified 77 differentially expressed circRNAs between mice fed with a normal diet and a high-fat diet. Surprisingly, multiple circRNAs were derived from the intron 2 of the preproinsulin 2 (Ins2) gene and are termed as circular intronic (ci)-Ins2. The expression of ci-Ins2 transcripts in mouse pancreatic islets, and βTC6 cells were confirmed by reverse transcription PCR, DNA sequencing, and RNase R treatment experiments. The level of ci-Ins2 was altered in βTC6 cells upon exposure to elevated levels of palmitate and glucose. Computational analysis predicted the interaction of several RNA-binding proteins with ci-Ins2 and their flanking region, suggesting their role in the ci-Ins2 function or biogenesis. Additionally, bioinformatics analysis predicted the association of several microRNAs with ci-Ins2. Gene ontology and pathway analysis of genes targeted by miRNAs associated with ci-Ins2 suggested the regulation of several key biological processes. Together, our findings indicate that differential expression of circRNAs, especially ci-Ins2 transcripts, may regulate β-cell function and may play a critical role in the development of diabetes. |
format | Online Article Text |
id | pubmed-7352490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73524902020-07-15 Identification and Characterization of Circular Intronic RNAs Derived from Insulin Gene Das, Debojyoti Das, Aniruddha Sahu, Mousumi Mishra, Smruti Sambhav Khan, Shaheerah Bejugam, Pruthvi R. Rout, Pranita K. Das, Arundhati Bano, Shehnaz Mishra, Gyan Prakash Raghav, Sunil K. Dixit, Anshuman Panda, Amaresh C. Int J Mol Sci Article Circular RNAs (circRNAs) are a large family of noncoding RNAs that have emerged as novel regulators of gene expression. However, little is known about the function of circRNAs in pancreatic β-cells. Here, transcriptomic analysis of mice pancreatic islet RNA-sequencing data identified 77 differentially expressed circRNAs between mice fed with a normal diet and a high-fat diet. Surprisingly, multiple circRNAs were derived from the intron 2 of the preproinsulin 2 (Ins2) gene and are termed as circular intronic (ci)-Ins2. The expression of ci-Ins2 transcripts in mouse pancreatic islets, and βTC6 cells were confirmed by reverse transcription PCR, DNA sequencing, and RNase R treatment experiments. The level of ci-Ins2 was altered in βTC6 cells upon exposure to elevated levels of palmitate and glucose. Computational analysis predicted the interaction of several RNA-binding proteins with ci-Ins2 and their flanking region, suggesting their role in the ci-Ins2 function or biogenesis. Additionally, bioinformatics analysis predicted the association of several microRNAs with ci-Ins2. Gene ontology and pathway analysis of genes targeted by miRNAs associated with ci-Ins2 suggested the regulation of several key biological processes. Together, our findings indicate that differential expression of circRNAs, especially ci-Ins2 transcripts, may regulate β-cell function and may play a critical role in the development of diabetes. MDPI 2020-06-17 /pmc/articles/PMC7352490/ /pubmed/32560282 http://dx.doi.org/10.3390/ijms21124302 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Das, Debojyoti Das, Aniruddha Sahu, Mousumi Mishra, Smruti Sambhav Khan, Shaheerah Bejugam, Pruthvi R. Rout, Pranita K. Das, Arundhati Bano, Shehnaz Mishra, Gyan Prakash Raghav, Sunil K. Dixit, Anshuman Panda, Amaresh C. Identification and Characterization of Circular Intronic RNAs Derived from Insulin Gene |
title | Identification and Characterization of Circular Intronic RNAs Derived from Insulin Gene |
title_full | Identification and Characterization of Circular Intronic RNAs Derived from Insulin Gene |
title_fullStr | Identification and Characterization of Circular Intronic RNAs Derived from Insulin Gene |
title_full_unstemmed | Identification and Characterization of Circular Intronic RNAs Derived from Insulin Gene |
title_short | Identification and Characterization of Circular Intronic RNAs Derived from Insulin Gene |
title_sort | identification and characterization of circular intronic rnas derived from insulin gene |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352490/ https://www.ncbi.nlm.nih.gov/pubmed/32560282 http://dx.doi.org/10.3390/ijms21124302 |
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