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The role of NUDT21 in microRNA‐binging sites of EZH2 gene increases the of risk preeclampsia

OBJECTIVES: Preeclampsia (PE) is a major cause of mortality and morbidity among pregnant mothers and their fetuses worldwide. Recent studies have shown that several microRNAs (miRNAs) play crucial role in pathogenesis of PE patients; however, the mechanisms responsible for differences in miRNA funct...

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Autores principales: Lang, Xiao, Zhao, Wenxia, Huang, Ding, Liu, Wei, Shen, Hong, Xu, Liang, Xu, Shan, Huang, Yongfang, Cheng, Weiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484293/
https://www.ncbi.nlm.nih.gov/pubmed/30883033
http://dx.doi.org/10.1111/jcmm.14179
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author Lang, Xiao
Zhao, Wenxia
Huang, Ding
Liu, Wei
Shen, Hong
Xu, Liang
Xu, Shan
Huang, Yongfang
Cheng, Weiwei
author_facet Lang, Xiao
Zhao, Wenxia
Huang, Ding
Liu, Wei
Shen, Hong
Xu, Liang
Xu, Shan
Huang, Yongfang
Cheng, Weiwei
author_sort Lang, Xiao
collection PubMed
description OBJECTIVES: Preeclampsia (PE) is a major cause of mortality and morbidity among pregnant mothers and their fetuses worldwide. Recent studies have shown that several microRNAs (miRNAs) play crucial role in pathogenesis of PE patients; however, the mechanisms responsible for differences in miRNA function in PE largely remain to be determined. MATERIALS AND METHODS: We studied that NUDT21 expression was markedly increased, whereas EZH2 was decreased in placental samples from patients with PE. We identified NUDT21 as an interaction partner of enhancer of zeste homologue 2 (EZH2). NUDT21 co‐localized with EZH2 in the human trophoblast cell line, HTR‐8/SVneo and NUDT21 was shown to bind to EZH2 in RNA immunoprecipitation assays. NUDT21 has previously been reported to be involved in alternative polyadenylation; thus, the interaction between NUDT21 and EZH2 may play an important role in the crosstalk between alternative polyadenylation (APA) and miRNA‐mediated gene silencing in PE. RESULTS: In the human trophoblast cell line HTR‐8/SVneo, loss‐of‐function assays indicated that knockdown of NUDT21 suppressed cell proliferation, migration and tube formation. Furthermore, functional studies showed that NUDT21 elongated the 3'‐UTR of mRNAs thereby exposing more miRNA binding sites (including miR138 and miR363), which enhanced the efficiency of miRNA‐mediated gene silencing and promoted EZH2 binding. CONCLUSIONS: This is the first report about the relationship of NUDT21 and EZH2. The data indicate that the aberrant expression of NUDT21 contributes to PE by targeting 3'‐UTR of EZH2 mRNA. These findings may provide novel targets for future investigations into therapeutic strategies for PE.
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spelling pubmed-64842932019-05-03 The role of NUDT21 in microRNA‐binging sites of EZH2 gene increases the of risk preeclampsia Lang, Xiao Zhao, Wenxia Huang, Ding Liu, Wei Shen, Hong Xu, Liang Xu, Shan Huang, Yongfang Cheng, Weiwei J Cell Mol Med Original Articles OBJECTIVES: Preeclampsia (PE) is a major cause of mortality and morbidity among pregnant mothers and their fetuses worldwide. Recent studies have shown that several microRNAs (miRNAs) play crucial role in pathogenesis of PE patients; however, the mechanisms responsible for differences in miRNA function in PE largely remain to be determined. MATERIALS AND METHODS: We studied that NUDT21 expression was markedly increased, whereas EZH2 was decreased in placental samples from patients with PE. We identified NUDT21 as an interaction partner of enhancer of zeste homologue 2 (EZH2). NUDT21 co‐localized with EZH2 in the human trophoblast cell line, HTR‐8/SVneo and NUDT21 was shown to bind to EZH2 in RNA immunoprecipitation assays. NUDT21 has previously been reported to be involved in alternative polyadenylation; thus, the interaction between NUDT21 and EZH2 may play an important role in the crosstalk between alternative polyadenylation (APA) and miRNA‐mediated gene silencing in PE. RESULTS: In the human trophoblast cell line HTR‐8/SVneo, loss‐of‐function assays indicated that knockdown of NUDT21 suppressed cell proliferation, migration and tube formation. Furthermore, functional studies showed that NUDT21 elongated the 3'‐UTR of mRNAs thereby exposing more miRNA binding sites (including miR138 and miR363), which enhanced the efficiency of miRNA‐mediated gene silencing and promoted EZH2 binding. CONCLUSIONS: This is the first report about the relationship of NUDT21 and EZH2. The data indicate that the aberrant expression of NUDT21 contributes to PE by targeting 3'‐UTR of EZH2 mRNA. These findings may provide novel targets for future investigations into therapeutic strategies for PE. John Wiley and Sons Inc. 2019-03-18 2019-05 /pmc/articles/PMC6484293/ /pubmed/30883033 http://dx.doi.org/10.1111/jcmm.14179 Text en © 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Lang, Xiao
Zhao, Wenxia
Huang, Ding
Liu, Wei
Shen, Hong
Xu, Liang
Xu, Shan
Huang, Yongfang
Cheng, Weiwei
The role of NUDT21 in microRNA‐binging sites of EZH2 gene increases the of risk preeclampsia
title The role of NUDT21 in microRNA‐binging sites of EZH2 gene increases the of risk preeclampsia
title_full The role of NUDT21 in microRNA‐binging sites of EZH2 gene increases the of risk preeclampsia
title_fullStr The role of NUDT21 in microRNA‐binging sites of EZH2 gene increases the of risk preeclampsia
title_full_unstemmed The role of NUDT21 in microRNA‐binging sites of EZH2 gene increases the of risk preeclampsia
title_short The role of NUDT21 in microRNA‐binging sites of EZH2 gene increases the of risk preeclampsia
title_sort role of nudt21 in microrna‐binging sites of ezh2 gene increases the of risk preeclampsia
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484293/
https://www.ncbi.nlm.nih.gov/pubmed/30883033
http://dx.doi.org/10.1111/jcmm.14179
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