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miR-423 sponged by lncRNA NORHA inhibits granulosa cell apoptosis
BACKGROUND: Atresia and degeneration, a follicular developmental fate that reduces female fertility and is triggered by granulosa cell (GC) apoptosis, have been induced by dozens of miRNAs. Here, we report a miRNA, miR-423, that inhibits the initiation of follicular atresia (FA), and early apoptosis...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696705/ http://dx.doi.org/10.1186/s40104-023-00960-y |
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author | Li, Yuqi Zhang, Zhuofan Wang, Siqi Du, Xing Li, Qifa |
author_facet | Li, Yuqi Zhang, Zhuofan Wang, Siqi Du, Xing Li, Qifa |
author_sort | Li, Yuqi |
collection | PubMed |
description | BACKGROUND: Atresia and degeneration, a follicular developmental fate that reduces female fertility and is triggered by granulosa cell (GC) apoptosis, have been induced by dozens of miRNAs. Here, we report a miRNA, miR-423, that inhibits the initiation of follicular atresia (FA), and early apoptosis of GCs. RESULTS: We showed that miR-423 was down-regulated during sow FA, and its levels in follicles were negatively correlated with the GC density and the P4/E2 ratio in the follicular fluid in vivo. The in vitro gain-of-function experiments revealed that miR-423 suppresses cell apoptosis, especially early apoptosis in GCs. Mechanically speaking, the miR-423 targets and interacts with the 3'-UTR of the porcine SMAD7 gene, which encodes an apoptosis-inducing factor in GCs, and represses its expression and pro-apoptotic function. Interestingly, FA and the GC apoptosis-related lncRNA NORHA was demonstrated as a ceRNA of miR-423. Additionally, we showed that a single base deletion/insertion in the miR-423 promoter is significantly associated with the number of stillbirths (NSB) trait of sows. CONCLUSION: These results demonstrate that miR-423 is a small molecule for inhibiting FA initiation and GC early apoptosis, suggesting that treating with miR-423 may be a novel approach for inhibiting FA initiation and improving female fertility. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-023-00960-y. |
format | Online Article Text |
id | pubmed-10696705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106967052023-12-06 miR-423 sponged by lncRNA NORHA inhibits granulosa cell apoptosis Li, Yuqi Zhang, Zhuofan Wang, Siqi Du, Xing Li, Qifa J Anim Sci Biotechnol Research BACKGROUND: Atresia and degeneration, a follicular developmental fate that reduces female fertility and is triggered by granulosa cell (GC) apoptosis, have been induced by dozens of miRNAs. Here, we report a miRNA, miR-423, that inhibits the initiation of follicular atresia (FA), and early apoptosis of GCs. RESULTS: We showed that miR-423 was down-regulated during sow FA, and its levels in follicles were negatively correlated with the GC density and the P4/E2 ratio in the follicular fluid in vivo. The in vitro gain-of-function experiments revealed that miR-423 suppresses cell apoptosis, especially early apoptosis in GCs. Mechanically speaking, the miR-423 targets and interacts with the 3'-UTR of the porcine SMAD7 gene, which encodes an apoptosis-inducing factor in GCs, and represses its expression and pro-apoptotic function. Interestingly, FA and the GC apoptosis-related lncRNA NORHA was demonstrated as a ceRNA of miR-423. Additionally, we showed that a single base deletion/insertion in the miR-423 promoter is significantly associated with the number of stillbirths (NSB) trait of sows. CONCLUSION: These results demonstrate that miR-423 is a small molecule for inhibiting FA initiation and GC early apoptosis, suggesting that treating with miR-423 may be a novel approach for inhibiting FA initiation and improving female fertility. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-023-00960-y. BioMed Central 2023-12-05 /pmc/articles/PMC10696705/ http://dx.doi.org/10.1186/s40104-023-00960-y Text en © The Author(s) 2023 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Li, Yuqi Zhang, Zhuofan Wang, Siqi Du, Xing Li, Qifa miR-423 sponged by lncRNA NORHA inhibits granulosa cell apoptosis |
title | miR-423 sponged by lncRNA NORHA inhibits granulosa cell apoptosis |
title_full | miR-423 sponged by lncRNA NORHA inhibits granulosa cell apoptosis |
title_fullStr | miR-423 sponged by lncRNA NORHA inhibits granulosa cell apoptosis |
title_full_unstemmed | miR-423 sponged by lncRNA NORHA inhibits granulosa cell apoptosis |
title_short | miR-423 sponged by lncRNA NORHA inhibits granulosa cell apoptosis |
title_sort | mir-423 sponged by lncrna norha inhibits granulosa cell apoptosis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696705/ http://dx.doi.org/10.1186/s40104-023-00960-y |
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