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Global Long Noncoding RNA and mRNA Expression Changes between Prenatal and Neonatal Lung Tissue in Pigs

Lung tissue plays an important role in the respiratory system of mammals after birth. Early lung development includes six key stages, of which the saccular stage spans the pre- and neonatal periods and prepares the distal lung for alveolarization and gas-exchange. However, little is known about the...

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Autores principales: Jin, Long, Hu, Silu, Tu, Teng, Huang, Zhiqing, Tang, Qianzi, Ma, Jideng, Wang, Xun, Li, Xuewei, Zhou, Xuan, Shuai, Surong, Li, Mingzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162397/
https://www.ncbi.nlm.nih.gov/pubmed/30189656
http://dx.doi.org/10.3390/genes9090443
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author Jin, Long
Hu, Silu
Tu, Teng
Huang, Zhiqing
Tang, Qianzi
Ma, Jideng
Wang, Xun
Li, Xuewei
Zhou, Xuan
Shuai, Surong
Li, Mingzhou
author_facet Jin, Long
Hu, Silu
Tu, Teng
Huang, Zhiqing
Tang, Qianzi
Ma, Jideng
Wang, Xun
Li, Xuewei
Zhou, Xuan
Shuai, Surong
Li, Mingzhou
author_sort Jin, Long
collection PubMed
description Lung tissue plays an important role in the respiratory system of mammals after birth. Early lung development includes six key stages, of which the saccular stage spans the pre- and neonatal periods and prepares the distal lung for alveolarization and gas-exchange. However, little is known about the changes in gene expression between fetal and neonatal lungs. In this study, we performed transcriptomic analysis of messenger RNA (mRNA) and long noncoding RNA (lncRNA) expressed in the lung tissue of fetal and neonatal piglets. A total of 19,310 lncRNAs and 14,579 mRNAs were identified and substantially expressed. Furthermore, 3248 mRNAs were significantly (FDR-adjusted p value ≤ 0.05, FDR: False Discovery Rate) differentially expressed and were mainly enriched in categories related to cell proliferation, immune response, hypoxia response, and mitochondrial activation. For example, CCNA2, an important gene involved in the cell cycle and DNA replication, was upregulated in neonatal lungs. We also identified 452 significantly (FDR-adjusted p value ≤ 0.05) differentially expressed lncRNAs, which might function in cell proliferation, mitochondrial activation, and immune response, similar to the differentially expressed mRNAs. These results suggest that differentially expressed mRNAs and lncRNAs might co-regulate lung development in early postnatal pigs. Notably, the TU64359 lncRNA might promote distal lung development by up-regulating the heparin-binding epidermal growth factor-like (HB-EGF) expression. Our research provides basic lung development datasets and will accelerate clinical researches of newborn lung diseases with pig models.
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spelling pubmed-61623972018-10-10 Global Long Noncoding RNA and mRNA Expression Changes between Prenatal and Neonatal Lung Tissue in Pigs Jin, Long Hu, Silu Tu, Teng Huang, Zhiqing Tang, Qianzi Ma, Jideng Wang, Xun Li, Xuewei Zhou, Xuan Shuai, Surong Li, Mingzhou Genes (Basel) Article Lung tissue plays an important role in the respiratory system of mammals after birth. Early lung development includes six key stages, of which the saccular stage spans the pre- and neonatal periods and prepares the distal lung for alveolarization and gas-exchange. However, little is known about the changes in gene expression between fetal and neonatal lungs. In this study, we performed transcriptomic analysis of messenger RNA (mRNA) and long noncoding RNA (lncRNA) expressed in the lung tissue of fetal and neonatal piglets. A total of 19,310 lncRNAs and 14,579 mRNAs were identified and substantially expressed. Furthermore, 3248 mRNAs were significantly (FDR-adjusted p value ≤ 0.05, FDR: False Discovery Rate) differentially expressed and were mainly enriched in categories related to cell proliferation, immune response, hypoxia response, and mitochondrial activation. For example, CCNA2, an important gene involved in the cell cycle and DNA replication, was upregulated in neonatal lungs. We also identified 452 significantly (FDR-adjusted p value ≤ 0.05) differentially expressed lncRNAs, which might function in cell proliferation, mitochondrial activation, and immune response, similar to the differentially expressed mRNAs. These results suggest that differentially expressed mRNAs and lncRNAs might co-regulate lung development in early postnatal pigs. Notably, the TU64359 lncRNA might promote distal lung development by up-regulating the heparin-binding epidermal growth factor-like (HB-EGF) expression. Our research provides basic lung development datasets and will accelerate clinical researches of newborn lung diseases with pig models. MDPI 2018-09-05 /pmc/articles/PMC6162397/ /pubmed/30189656 http://dx.doi.org/10.3390/genes9090443 Text en © 2018 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
Jin, Long
Hu, Silu
Tu, Teng
Huang, Zhiqing
Tang, Qianzi
Ma, Jideng
Wang, Xun
Li, Xuewei
Zhou, Xuan
Shuai, Surong
Li, Mingzhou
Global Long Noncoding RNA and mRNA Expression Changes between Prenatal and Neonatal Lung Tissue in Pigs
title Global Long Noncoding RNA and mRNA Expression Changes between Prenatal and Neonatal Lung Tissue in Pigs
title_full Global Long Noncoding RNA and mRNA Expression Changes between Prenatal and Neonatal Lung Tissue in Pigs
title_fullStr Global Long Noncoding RNA and mRNA Expression Changes between Prenatal and Neonatal Lung Tissue in Pigs
title_full_unstemmed Global Long Noncoding RNA and mRNA Expression Changes between Prenatal and Neonatal Lung Tissue in Pigs
title_short Global Long Noncoding RNA and mRNA Expression Changes between Prenatal and Neonatal Lung Tissue in Pigs
title_sort global long noncoding rna and mrna expression changes between prenatal and neonatal lung tissue in pigs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162397/
https://www.ncbi.nlm.nih.gov/pubmed/30189656
http://dx.doi.org/10.3390/genes9090443
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