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Identification, functional prediction, and key lncRNA verification of cold stress-related lncRNAs in rats liver

Cold stimulation reduces the quality of animal products and increases animal mortality, causing huge losses to the livestock industry in cold regions. Long non-coding RNAs (lncRNAs) take part in many biological processes through transcriptional regulation, intracellular material transport, and chrom...

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Autores principales: Ji, Hong, Niu, Chunyang, Zhan, Xuelong, Xu, Jing, Lian, Shuai, Xu, Bin, Guo, Jingru, Zhen, Li, Yang, Huanmin, Li, Shize, Ma, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965121/
https://www.ncbi.nlm.nih.gov/pubmed/31949263
http://dx.doi.org/10.1038/s41598-020-57451-7
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author Ji, Hong
Niu, Chunyang
Zhan, Xuelong
Xu, Jing
Lian, Shuai
Xu, Bin
Guo, Jingru
Zhen, Li
Yang, Huanmin
Li, Shize
Ma, Li
author_facet Ji, Hong
Niu, Chunyang
Zhan, Xuelong
Xu, Jing
Lian, Shuai
Xu, Bin
Guo, Jingru
Zhen, Li
Yang, Huanmin
Li, Shize
Ma, Li
author_sort Ji, Hong
collection PubMed
description Cold stimulation reduces the quality of animal products and increases animal mortality, causing huge losses to the livestock industry in cold regions. Long non-coding RNAs (lncRNAs) take part in many biological processes through transcriptional regulation, intracellular material transport, and chromosome remodeling. Although cold stress-related lncRNAs have been reported in plants, no research is available on the characteristic and functional analysis of lncRNAs after cold stress in rats. Here, we built a cold stress animal model firstly. Six SPF male Wistar rats were randomly divided to the acute cold stress group (4 °C, 12 h) and the normal group (24 °C, 12 h). lncRNA libraries were constructed by high-throughput sequencing (HTS) using rat livers. 2,120 new lncRNAs and 273 differentially expressed (DE) lncRNAs were identified in low temperature environments. The target genes of DElncRNA were predicted by cis and trans, and then functional and pathway analysis were performed to them. GO and KEGG analysis revealed that lncRNA targets were mainly participated in the regulation of nucleic acid binding, cold stimulation reaction, metabolic process, immune system processes, PI3K-Akt signaling pathway and pathways in cancer. Next, a interaction network between lncRNA and its targets was constructed. To further reveal the mechanism of cold stress, DElncRNA and DEmRNA were extracted to reconstruct a co-expression sub-network. We found the key lncRNA MSTRG.80946.2 in sub-network. Functional analysis of key lncRNA targets showed that targets were significantly enriched in fatty acid metabolism, the PI3K-Akt signaling pathway and pathways in cancer under cold stress. qRT-PCR confirmed the sequencing results. Finally, hub lncRNA MSTRG.80946.2 was characterized, and verified its relationship with related mRNAs by antisense oligonucleotide (ASO) interference and qRT-PCR. Results confirmed the accuracy of our analysis. To sum up, our work was the first to perform detailed characterization and functional analysis of cold stress-related lncRNAs in rats liver. lncRNAs played crucial roles in energy metabolism, growth and development, immunity and reproductive performance in cold stressed rats. The MSTRG.80946.2 was verified by network and experiments to be a key functional lncRNA under cold stress, regulating ACP1, TSPY1 and Tsn.
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spelling pubmed-69651212020-01-23 Identification, functional prediction, and key lncRNA verification of cold stress-related lncRNAs in rats liver Ji, Hong Niu, Chunyang Zhan, Xuelong Xu, Jing Lian, Shuai Xu, Bin Guo, Jingru Zhen, Li Yang, Huanmin Li, Shize Ma, Li Sci Rep Article Cold stimulation reduces the quality of animal products and increases animal mortality, causing huge losses to the livestock industry in cold regions. Long non-coding RNAs (lncRNAs) take part in many biological processes through transcriptional regulation, intracellular material transport, and chromosome remodeling. Although cold stress-related lncRNAs have been reported in plants, no research is available on the characteristic and functional analysis of lncRNAs after cold stress in rats. Here, we built a cold stress animal model firstly. Six SPF male Wistar rats were randomly divided to the acute cold stress group (4 °C, 12 h) and the normal group (24 °C, 12 h). lncRNA libraries were constructed by high-throughput sequencing (HTS) using rat livers. 2,120 new lncRNAs and 273 differentially expressed (DE) lncRNAs were identified in low temperature environments. The target genes of DElncRNA were predicted by cis and trans, and then functional and pathway analysis were performed to them. GO and KEGG analysis revealed that lncRNA targets were mainly participated in the regulation of nucleic acid binding, cold stimulation reaction, metabolic process, immune system processes, PI3K-Akt signaling pathway and pathways in cancer. Next, a interaction network between lncRNA and its targets was constructed. To further reveal the mechanism of cold stress, DElncRNA and DEmRNA were extracted to reconstruct a co-expression sub-network. We found the key lncRNA MSTRG.80946.2 in sub-network. Functional analysis of key lncRNA targets showed that targets were significantly enriched in fatty acid metabolism, the PI3K-Akt signaling pathway and pathways in cancer under cold stress. qRT-PCR confirmed the sequencing results. Finally, hub lncRNA MSTRG.80946.2 was characterized, and verified its relationship with related mRNAs by antisense oligonucleotide (ASO) interference and qRT-PCR. Results confirmed the accuracy of our analysis. To sum up, our work was the first to perform detailed characterization and functional analysis of cold stress-related lncRNAs in rats liver. lncRNAs played crucial roles in energy metabolism, growth and development, immunity and reproductive performance in cold stressed rats. The MSTRG.80946.2 was verified by network and experiments to be a key functional lncRNA under cold stress, regulating ACP1, TSPY1 and Tsn. Nature Publishing Group UK 2020-01-16 /pmc/articles/PMC6965121/ /pubmed/31949263 http://dx.doi.org/10.1038/s41598-020-57451-7 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ji, Hong
Niu, Chunyang
Zhan, Xuelong
Xu, Jing
Lian, Shuai
Xu, Bin
Guo, Jingru
Zhen, Li
Yang, Huanmin
Li, Shize
Ma, Li
Identification, functional prediction, and key lncRNA verification of cold stress-related lncRNAs in rats liver
title Identification, functional prediction, and key lncRNA verification of cold stress-related lncRNAs in rats liver
title_full Identification, functional prediction, and key lncRNA verification of cold stress-related lncRNAs in rats liver
title_fullStr Identification, functional prediction, and key lncRNA verification of cold stress-related lncRNAs in rats liver
title_full_unstemmed Identification, functional prediction, and key lncRNA verification of cold stress-related lncRNAs in rats liver
title_short Identification, functional prediction, and key lncRNA verification of cold stress-related lncRNAs in rats liver
title_sort identification, functional prediction, and key lncrna verification of cold stress-related lncrnas in rats liver
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965121/
https://www.ncbi.nlm.nih.gov/pubmed/31949263
http://dx.doi.org/10.1038/s41598-020-57451-7
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