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IRLnc: a novel functional noncoding RNA contributes to intramuscular fat deposition
BACKGROUND: Intramuscular fat (IMF) is associated with meat quality and insulin resistance in animals. Research on genetic mechanism of IMF decomposition has positive meaning to pork quality and diseases such as obesity and type 2 diabetes treatment. In this study, an IMF trait segregation populatio...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849149/ https://www.ncbi.nlm.nih.gov/pubmed/33522899 http://dx.doi.org/10.1186/s12864-020-07349-5 |
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author | Wang, Ligang Zhou, Zhong-Yin Zhang, Tian Zhang, Longchao Hou, Xinhua Yan, Hua Wang, Lixian |
author_facet | Wang, Ligang Zhou, Zhong-Yin Zhang, Tian Zhang, Longchao Hou, Xinhua Yan, Hua Wang, Lixian |
author_sort | Wang, Ligang |
collection | PubMed |
description | BACKGROUND: Intramuscular fat (IMF) is associated with meat quality and insulin resistance in animals. Research on genetic mechanism of IMF decomposition has positive meaning to pork quality and diseases such as obesity and type 2 diabetes treatment. In this study, an IMF trait segregation population was used to perform RNA sequencing and to analyze the joint or independent effects of genes and long intergenic non-coding RNAs (lincRNAs) on IMF. RESULTS: A total of 26 genes including six lincRNA genes show significantly different expression between high- and low-IMF pigs. Interesting, one lincRNA gene, named IMF related lincRNA (IRLnc) not only has a 292-bp conserved region in 100 vertebrates but also has conserved up and down stream genes (< 10 kb) in pig and humans. Real-time quantitative polymerase chain reaction (RT-qPCR) validation study indicated that nuclear receptor subfamily 4 group A member 3 (NR4A3) which located at the downstream of IRLnc has similar expression pattern with IRLnc. RNAi-mediated loss of function screens identified that IRLnc silencing could inhibit both of the RNA and protein expression of NR4A3. And the in-situ hybridization co-expression experiment indicates that IRLnc may directly binding to NR4A3. As the NR4A3 could regulate the catecholamine catabolism, which could affect insulin sensitivity, we inferred that IRLnc influence IMF decomposition by regulating the expression of NR4A3. CONCLUSIONS: In conclusion, a novel functional noncoding variation named IRLnc has been found contribute to IMF by regulating the expression of NR4A3. These findings suggest novel mechanistic approach for treatment of insulin resistance in human beings and meat quality improvement in animal. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-020-07349-5. |
format | Online Article Text |
id | pubmed-7849149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78491492021-02-03 IRLnc: a novel functional noncoding RNA contributes to intramuscular fat deposition Wang, Ligang Zhou, Zhong-Yin Zhang, Tian Zhang, Longchao Hou, Xinhua Yan, Hua Wang, Lixian BMC Genomics Research Article BACKGROUND: Intramuscular fat (IMF) is associated with meat quality and insulin resistance in animals. Research on genetic mechanism of IMF decomposition has positive meaning to pork quality and diseases such as obesity and type 2 diabetes treatment. In this study, an IMF trait segregation population was used to perform RNA sequencing and to analyze the joint or independent effects of genes and long intergenic non-coding RNAs (lincRNAs) on IMF. RESULTS: A total of 26 genes including six lincRNA genes show significantly different expression between high- and low-IMF pigs. Interesting, one lincRNA gene, named IMF related lincRNA (IRLnc) not only has a 292-bp conserved region in 100 vertebrates but also has conserved up and down stream genes (< 10 kb) in pig and humans. Real-time quantitative polymerase chain reaction (RT-qPCR) validation study indicated that nuclear receptor subfamily 4 group A member 3 (NR4A3) which located at the downstream of IRLnc has similar expression pattern with IRLnc. RNAi-mediated loss of function screens identified that IRLnc silencing could inhibit both of the RNA and protein expression of NR4A3. And the in-situ hybridization co-expression experiment indicates that IRLnc may directly binding to NR4A3. As the NR4A3 could regulate the catecholamine catabolism, which could affect insulin sensitivity, we inferred that IRLnc influence IMF decomposition by regulating the expression of NR4A3. CONCLUSIONS: In conclusion, a novel functional noncoding variation named IRLnc has been found contribute to IMF by regulating the expression of NR4A3. These findings suggest novel mechanistic approach for treatment of insulin resistance in human beings and meat quality improvement in animal. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-020-07349-5. BioMed Central 2021-02-01 /pmc/articles/PMC7849149/ /pubmed/33522899 http://dx.doi.org/10.1186/s12864-020-07349-5 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Wang, Ligang Zhou, Zhong-Yin Zhang, Tian Zhang, Longchao Hou, Xinhua Yan, Hua Wang, Lixian IRLnc: a novel functional noncoding RNA contributes to intramuscular fat deposition |
title | IRLnc: a novel functional noncoding RNA contributes to intramuscular fat deposition |
title_full | IRLnc: a novel functional noncoding RNA contributes to intramuscular fat deposition |
title_fullStr | IRLnc: a novel functional noncoding RNA contributes to intramuscular fat deposition |
title_full_unstemmed | IRLnc: a novel functional noncoding RNA contributes to intramuscular fat deposition |
title_short | IRLnc: a novel functional noncoding RNA contributes to intramuscular fat deposition |
title_sort | irlnc: a novel functional noncoding rna contributes to intramuscular fat deposition |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849149/ https://www.ncbi.nlm.nih.gov/pubmed/33522899 http://dx.doi.org/10.1186/s12864-020-07349-5 |
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