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Transcriptome Profiling of Placenta through Pregnancy Reveals Dysregulation of Bile Acids Transport and Detoxification Function

Placenta performs the function of several adult organs for the fetus during intrauterine life. Because of the dramatic physiological and metabolic changes during pregnancy and the strong association between maternal metabolism and placental function, the possibility that variation in gene expression...

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Autores principales: Wang, Peng, Song, Yumo, Zhong, Heju, Lin, Sen, Zhang, Xiaoling, Li, Jian, Che, Lianqiang, Feng, Bin, Lin, Yan, Xu, Shengyu, Zhuo, Yong, Wu, De, Burrin, Douglas G., Fang, Zhengfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6747679/
https://www.ncbi.nlm.nih.gov/pubmed/31443432
http://dx.doi.org/10.3390/ijms20174099
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author Wang, Peng
Song, Yumo
Zhong, Heju
Lin, Sen
Zhang, Xiaoling
Li, Jian
Che, Lianqiang
Feng, Bin
Lin, Yan
Xu, Shengyu
Zhuo, Yong
Wu, De
Burrin, Douglas G.
Fang, Zhengfeng
author_facet Wang, Peng
Song, Yumo
Zhong, Heju
Lin, Sen
Zhang, Xiaoling
Li, Jian
Che, Lianqiang
Feng, Bin
Lin, Yan
Xu, Shengyu
Zhuo, Yong
Wu, De
Burrin, Douglas G.
Fang, Zhengfeng
author_sort Wang, Peng
collection PubMed
description Placenta performs the function of several adult organs for the fetus during intrauterine life. Because of the dramatic physiological and metabolic changes during pregnancy and the strong association between maternal metabolism and placental function, the possibility that variation in gene expression patterns during pregnancy might be linked to fetal health warrants investigation. Here, next-generation RNA sequencing was used to investigate the expression profile, including mRNAs and long non-coding RNAs (lncRNAs) of placentas on day 60 of gestation (G60), day 90 of gestation (G90), and on the farrowing day (L0) in pregnant swine. Bioinformatics analysis of differentially expressed mRNAs and lncRNAs consistently showed dysregulation of bile acids transport and detoxification as pregnancy progress. We found the differentially expressed mRNAs, particularly bile salt export pump (ABCB11), organic anion-transporting polypeptide 1A2 (OATP1A2), carbonic anhydrase II (CA2), Na(+)-HCO(3)(−) cotransporter (NBC1), and hydroxysteroid sulfotransferases (SULT2A1) play an important role in bile acids transport and sulfation in placentas during pregnancy. We also found the potential regulation role of ALDBSSCG0000000220 and XLOC_1301271 on placental SULT2A1. These findings have uncovered a previously unclear function and its genetic basis for bile acids metabolism in developing placentas and have important implications for exploring the potential physiological and pathological pathway to improve fetal outcomes.
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spelling pubmed-67476792019-09-27 Transcriptome Profiling of Placenta through Pregnancy Reveals Dysregulation of Bile Acids Transport and Detoxification Function Wang, Peng Song, Yumo Zhong, Heju Lin, Sen Zhang, Xiaoling Li, Jian Che, Lianqiang Feng, Bin Lin, Yan Xu, Shengyu Zhuo, Yong Wu, De Burrin, Douglas G. Fang, Zhengfeng Int J Mol Sci Article Placenta performs the function of several adult organs for the fetus during intrauterine life. Because of the dramatic physiological and metabolic changes during pregnancy and the strong association between maternal metabolism and placental function, the possibility that variation in gene expression patterns during pregnancy might be linked to fetal health warrants investigation. Here, next-generation RNA sequencing was used to investigate the expression profile, including mRNAs and long non-coding RNAs (lncRNAs) of placentas on day 60 of gestation (G60), day 90 of gestation (G90), and on the farrowing day (L0) in pregnant swine. Bioinformatics analysis of differentially expressed mRNAs and lncRNAs consistently showed dysregulation of bile acids transport and detoxification as pregnancy progress. We found the differentially expressed mRNAs, particularly bile salt export pump (ABCB11), organic anion-transporting polypeptide 1A2 (OATP1A2), carbonic anhydrase II (CA2), Na(+)-HCO(3)(−) cotransporter (NBC1), and hydroxysteroid sulfotransferases (SULT2A1) play an important role in bile acids transport and sulfation in placentas during pregnancy. We also found the potential regulation role of ALDBSSCG0000000220 and XLOC_1301271 on placental SULT2A1. These findings have uncovered a previously unclear function and its genetic basis for bile acids metabolism in developing placentas and have important implications for exploring the potential physiological and pathological pathway to improve fetal outcomes. MDPI 2019-08-22 /pmc/articles/PMC6747679/ /pubmed/31443432 http://dx.doi.org/10.3390/ijms20174099 Text en © 2019 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
Wang, Peng
Song, Yumo
Zhong, Heju
Lin, Sen
Zhang, Xiaoling
Li, Jian
Che, Lianqiang
Feng, Bin
Lin, Yan
Xu, Shengyu
Zhuo, Yong
Wu, De
Burrin, Douglas G.
Fang, Zhengfeng
Transcriptome Profiling of Placenta through Pregnancy Reveals Dysregulation of Bile Acids Transport and Detoxification Function
title Transcriptome Profiling of Placenta through Pregnancy Reveals Dysregulation of Bile Acids Transport and Detoxification Function
title_full Transcriptome Profiling of Placenta through Pregnancy Reveals Dysregulation of Bile Acids Transport and Detoxification Function
title_fullStr Transcriptome Profiling of Placenta through Pregnancy Reveals Dysregulation of Bile Acids Transport and Detoxification Function
title_full_unstemmed Transcriptome Profiling of Placenta through Pregnancy Reveals Dysregulation of Bile Acids Transport and Detoxification Function
title_short Transcriptome Profiling of Placenta through Pregnancy Reveals Dysregulation of Bile Acids Transport and Detoxification Function
title_sort transcriptome profiling of placenta through pregnancy reveals dysregulation of bile acids transport and detoxification function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6747679/
https://www.ncbi.nlm.nih.gov/pubmed/31443432
http://dx.doi.org/10.3390/ijms20174099
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