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Transcriptome-wide analysis of the SCNT bovine abnormal placenta during mid- to late gestation
The dysfunction of placenta is common in somatic cell nuclear transfer (SCNT) cloned cattle and would cause aberrant fetal development and even abortion, which occurred with highest rate at the mid- to late gestation. However, the mechanism of abnormal placentas was unclear. To analyze the transcrip...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934727/ https://www.ncbi.nlm.nih.gov/pubmed/31882783 http://dx.doi.org/10.1038/s41598-019-56566-w |
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author | Gao, Guangqi Wang, Shenyuan Zhang, Jiaqi Su, Guanghua Zheng, Zhong Bai, Chunling Yang, Lei Wei, Zhuying Wang, Xiuying Liu, Xiao Guo, Ziru Li, Guangpeng Su, Xiaohu Zhang, Li |
author_facet | Gao, Guangqi Wang, Shenyuan Zhang, Jiaqi Su, Guanghua Zheng, Zhong Bai, Chunling Yang, Lei Wei, Zhuying Wang, Xiuying Liu, Xiao Guo, Ziru Li, Guangpeng Su, Xiaohu Zhang, Li |
author_sort | Gao, Guangqi |
collection | PubMed |
description | The dysfunction of placenta is common in somatic cell nuclear transfer (SCNT) cloned cattle and would cause aberrant fetal development and even abortion, which occurred with highest rate at the mid- to late gestation. However, the mechanism of abnormal placentas was unclear. To analyze the transcriptome-wide characteristics of abnormal placentas in SCNT cloned cattle, the mRNA, lncRNA and miRNA of placental cotyledon tissue at day 180 after gestation were sequenced. A total of 19,055 mRNAs, 30,141 lncRNAs and 684 miRNAs were identified. Compared with control group, 362 mRNAs, 1,272 lncRNAs and nine miRNAs (six known and three novel miRNAs) were differentially expressed (fold change ≥ 2 and P-value < 0.05). The differentially expressed genes were functionally enriched in urea and ions transmembrane transport, which indicated that the maternal-fetal interactions were disturbed in impaired placentas. Furthermore, the competing endogenous RNAs (ceRNAs) networks were identified to illustrate their roles in abnormal placental morphology. The present research would be helpful to discover the mechanism of late gestational abnormality of SCNT cattle by provides important genomic information and insights. |
format | Online Article Text |
id | pubmed-6934727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69347272019-12-30 Transcriptome-wide analysis of the SCNT bovine abnormal placenta during mid- to late gestation Gao, Guangqi Wang, Shenyuan Zhang, Jiaqi Su, Guanghua Zheng, Zhong Bai, Chunling Yang, Lei Wei, Zhuying Wang, Xiuying Liu, Xiao Guo, Ziru Li, Guangpeng Su, Xiaohu Zhang, Li Sci Rep Article The dysfunction of placenta is common in somatic cell nuclear transfer (SCNT) cloned cattle and would cause aberrant fetal development and even abortion, which occurred with highest rate at the mid- to late gestation. However, the mechanism of abnormal placentas was unclear. To analyze the transcriptome-wide characteristics of abnormal placentas in SCNT cloned cattle, the mRNA, lncRNA and miRNA of placental cotyledon tissue at day 180 after gestation were sequenced. A total of 19,055 mRNAs, 30,141 lncRNAs and 684 miRNAs were identified. Compared with control group, 362 mRNAs, 1,272 lncRNAs and nine miRNAs (six known and three novel miRNAs) were differentially expressed (fold change ≥ 2 and P-value < 0.05). The differentially expressed genes were functionally enriched in urea and ions transmembrane transport, which indicated that the maternal-fetal interactions were disturbed in impaired placentas. Furthermore, the competing endogenous RNAs (ceRNAs) networks were identified to illustrate their roles in abnormal placental morphology. The present research would be helpful to discover the mechanism of late gestational abnormality of SCNT cattle by provides important genomic information and insights. Nature Publishing Group UK 2019-12-27 /pmc/articles/PMC6934727/ /pubmed/31882783 http://dx.doi.org/10.1038/s41598-019-56566-w Text en © The Author(s) 2019 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 Gao, Guangqi Wang, Shenyuan Zhang, Jiaqi Su, Guanghua Zheng, Zhong Bai, Chunling Yang, Lei Wei, Zhuying Wang, Xiuying Liu, Xiao Guo, Ziru Li, Guangpeng Su, Xiaohu Zhang, Li Transcriptome-wide analysis of the SCNT bovine abnormal placenta during mid- to late gestation |
title | Transcriptome-wide analysis of the SCNT bovine abnormal placenta during mid- to late gestation |
title_full | Transcriptome-wide analysis of the SCNT bovine abnormal placenta during mid- to late gestation |
title_fullStr | Transcriptome-wide analysis of the SCNT bovine abnormal placenta during mid- to late gestation |
title_full_unstemmed | Transcriptome-wide analysis of the SCNT bovine abnormal placenta during mid- to late gestation |
title_short | Transcriptome-wide analysis of the SCNT bovine abnormal placenta during mid- to late gestation |
title_sort | transcriptome-wide analysis of the scnt bovine abnormal placenta during mid- to late gestation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934727/ https://www.ncbi.nlm.nih.gov/pubmed/31882783 http://dx.doi.org/10.1038/s41598-019-56566-w |
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