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Identification and characterization of Piwi-interacting RNAs in human placentas of preeclampsia
Preeclampsia is a common disease of pregnancy that poses a serious threat to the safety of pregnant women and the fetus; however, the etiology of preeclampsia is inconclusive. Piwi-interacting RNAs (piRNAs) are novel non-coding RNAs that are present at high levels in germ cells and are associated wi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333249/ https://www.ncbi.nlm.nih.gov/pubmed/34344990 http://dx.doi.org/10.1038/s41598-021-95307-w |
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author | He, Jie Chen, Miaomiao Xu, Jiacheng Fang, Jie Liu, Zheng Qi, Hongbo |
author_facet | He, Jie Chen, Miaomiao Xu, Jiacheng Fang, Jie Liu, Zheng Qi, Hongbo |
author_sort | He, Jie |
collection | PubMed |
description | Preeclampsia is a common disease of pregnancy that poses a serious threat to the safety of pregnant women and the fetus; however, the etiology of preeclampsia is inconclusive. Piwi-interacting RNAs (piRNAs) are novel non-coding RNAs that are present at high levels in germ cells and are associated with spermatogenesis. Emerging evidence demonstrated that piRNA is expressed in a variety of human tissues and is closely associated with tumorigenesis. However, changes in the piRNA expression profile in the placenta have not been investigated. In this study, we used small RNA sequencing to evaluate the differences in piRNA expression profiles between preeclampsia and control patients and potential functions. Differential expression analysis found 41 up-regulated and 36 down-regulated piRNAs in preeclamptic samples. In addition, the functional enrichment analysis of piRNAs target genes indicated that they were related to the extracellular matrix (ECM) formation and tissue-specific. Finally, we examined the expression pattern of the PIWL family proteins in the placenta, and PIWL3 and PIWIL4 were the primary subtypes in the human placenta. In summary, this study first summarized the changes in the expression pattern of piRNA in preeclampsia and provided new clues for the regulatory role of piRNA in the human placenta. |
format | Online Article Text |
id | pubmed-8333249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83332492021-08-04 Identification and characterization of Piwi-interacting RNAs in human placentas of preeclampsia He, Jie Chen, Miaomiao Xu, Jiacheng Fang, Jie Liu, Zheng Qi, Hongbo Sci Rep Article Preeclampsia is a common disease of pregnancy that poses a serious threat to the safety of pregnant women and the fetus; however, the etiology of preeclampsia is inconclusive. Piwi-interacting RNAs (piRNAs) are novel non-coding RNAs that are present at high levels in germ cells and are associated with spermatogenesis. Emerging evidence demonstrated that piRNA is expressed in a variety of human tissues and is closely associated with tumorigenesis. However, changes in the piRNA expression profile in the placenta have not been investigated. In this study, we used small RNA sequencing to evaluate the differences in piRNA expression profiles between preeclampsia and control patients and potential functions. Differential expression analysis found 41 up-regulated and 36 down-regulated piRNAs in preeclamptic samples. In addition, the functional enrichment analysis of piRNAs target genes indicated that they were related to the extracellular matrix (ECM) formation and tissue-specific. Finally, we examined the expression pattern of the PIWL family proteins in the placenta, and PIWL3 and PIWIL4 were the primary subtypes in the human placenta. In summary, this study first summarized the changes in the expression pattern of piRNA in preeclampsia and provided new clues for the regulatory role of piRNA in the human placenta. Nature Publishing Group UK 2021-08-03 /pmc/articles/PMC8333249/ /pubmed/34344990 http://dx.doi.org/10.1038/s41598-021-95307-w Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article He, Jie Chen, Miaomiao Xu, Jiacheng Fang, Jie Liu, Zheng Qi, Hongbo Identification and characterization of Piwi-interacting RNAs in human placentas of preeclampsia |
title | Identification and characterization of Piwi-interacting RNAs in human placentas of preeclampsia |
title_full | Identification and characterization of Piwi-interacting RNAs in human placentas of preeclampsia |
title_fullStr | Identification and characterization of Piwi-interacting RNAs in human placentas of preeclampsia |
title_full_unstemmed | Identification and characterization of Piwi-interacting RNAs in human placentas of preeclampsia |
title_short | Identification and characterization of Piwi-interacting RNAs in human placentas of preeclampsia |
title_sort | identification and characterization of piwi-interacting rnas in human placentas of preeclampsia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333249/ https://www.ncbi.nlm.nih.gov/pubmed/34344990 http://dx.doi.org/10.1038/s41598-021-95307-w |
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