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Identification and Functional Prediction of Long Intergenic Non-coding RNAs Related to Subcutaneous Adipose Development in Pigs

An increasing number of studies have shown that long intergenic non-coding RNAs (lincRNAs) are a very important class of non-coding RNAs that plays a vital role in many biological processes. Adipose tissue is an important place for storing energy, but few studies on lincRNAs were related to pig subc...

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Autores principales: Shi, Gaoli, Chen, Lin, Chen, Guoting, Zou, Cheng, Li, Jingxuan, Li, Mengxun, Fang, Chengchi, Li, Changchun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409335/
https://www.ncbi.nlm.nih.gov/pubmed/30886630
http://dx.doi.org/10.3389/fgene.2019.00160
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author Shi, Gaoli
Chen, Lin
Chen, Guoting
Zou, Cheng
Li, Jingxuan
Li, Mengxun
Fang, Chengchi
Li, Changchun
author_facet Shi, Gaoli
Chen, Lin
Chen, Guoting
Zou, Cheng
Li, Jingxuan
Li, Mengxun
Fang, Chengchi
Li, Changchun
author_sort Shi, Gaoli
collection PubMed
description An increasing number of studies have shown that long intergenic non-coding RNAs (lincRNAs) are a very important class of non-coding RNAs that plays a vital role in many biological processes. Adipose tissue is an important place for storing energy, but few studies on lincRNAs were related to pig subcutaneous fat development. Here, we used published RNA-seq data from subcutaneous adipose tissue of Italian Large White pigs and identified 252 putative lincRNAs, wherein 34 were unannotated. These lincRNAs had relatively shorter length, lower number of exons, and lower expression level compared with protein-coding transcripts. Gene ontology and pathway analysis indicated that the adjacent genes of lincRNAs were involved in lipid metabolism. In addition, differentially expressed lincRNAs (DELs) between low and high backfat thickness pigs were identified. Through the detection of quantitative trait locus (QTL), DELs were mainly located in QTLs related to adipose development. Based on the expression correlation of DEL genes and their differentially expressed potential target genes, we constructed a co-expression network and a potential pathway of DEL’s effect on lipid metabolism. Our study identified and analyzed lincRNAs in subcutaneous adipose tissue, and results suggested that lincRNAs may be involved in the regulation of subcutaneous fat development. Our findings provided new insights into the biological function of porcine lincRNAs.
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spelling pubmed-64093352019-03-18 Identification and Functional Prediction of Long Intergenic Non-coding RNAs Related to Subcutaneous Adipose Development in Pigs Shi, Gaoli Chen, Lin Chen, Guoting Zou, Cheng Li, Jingxuan Li, Mengxun Fang, Chengchi Li, Changchun Front Genet Genetics An increasing number of studies have shown that long intergenic non-coding RNAs (lincRNAs) are a very important class of non-coding RNAs that plays a vital role in many biological processes. Adipose tissue is an important place for storing energy, but few studies on lincRNAs were related to pig subcutaneous fat development. Here, we used published RNA-seq data from subcutaneous adipose tissue of Italian Large White pigs and identified 252 putative lincRNAs, wherein 34 were unannotated. These lincRNAs had relatively shorter length, lower number of exons, and lower expression level compared with protein-coding transcripts. Gene ontology and pathway analysis indicated that the adjacent genes of lincRNAs were involved in lipid metabolism. In addition, differentially expressed lincRNAs (DELs) between low and high backfat thickness pigs were identified. Through the detection of quantitative trait locus (QTL), DELs were mainly located in QTLs related to adipose development. Based on the expression correlation of DEL genes and their differentially expressed potential target genes, we constructed a co-expression network and a potential pathway of DEL’s effect on lipid metabolism. Our study identified and analyzed lincRNAs in subcutaneous adipose tissue, and results suggested that lincRNAs may be involved in the regulation of subcutaneous fat development. Our findings provided new insights into the biological function of porcine lincRNAs. Frontiers Media S.A. 2019-03-04 /pmc/articles/PMC6409335/ /pubmed/30886630 http://dx.doi.org/10.3389/fgene.2019.00160 Text en Copyright © 2019 Shi, Chen, Chen, Zou, Li, Li, Fang and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Shi, Gaoli
Chen, Lin
Chen, Guoting
Zou, Cheng
Li, Jingxuan
Li, Mengxun
Fang, Chengchi
Li, Changchun
Identification and Functional Prediction of Long Intergenic Non-coding RNAs Related to Subcutaneous Adipose Development in Pigs
title Identification and Functional Prediction of Long Intergenic Non-coding RNAs Related to Subcutaneous Adipose Development in Pigs
title_full Identification and Functional Prediction of Long Intergenic Non-coding RNAs Related to Subcutaneous Adipose Development in Pigs
title_fullStr Identification and Functional Prediction of Long Intergenic Non-coding RNAs Related to Subcutaneous Adipose Development in Pigs
title_full_unstemmed Identification and Functional Prediction of Long Intergenic Non-coding RNAs Related to Subcutaneous Adipose Development in Pigs
title_short Identification and Functional Prediction of Long Intergenic Non-coding RNAs Related to Subcutaneous Adipose Development in Pigs
title_sort identification and functional prediction of long intergenic non-coding rnas related to subcutaneous adipose development in pigs
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409335/
https://www.ncbi.nlm.nih.gov/pubmed/30886630
http://dx.doi.org/10.3389/fgene.2019.00160
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