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Genistein up-regulates miR-20a to disrupt spermatogenesis via targeting Limk1
Genistein (GEN) is one of the isoflavones that has effect on male reproduction. However, the underlying mechanism remains unknown. miRNAs are a type of small non-coding RNAs that play important roles in spermatogenesis. We measured the GEN levels and miR-17-92 cluster expression in infertile subject...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601687/ https://www.ncbi.nlm.nih.gov/pubmed/28938591 http://dx.doi.org/10.18632/oncotarget.17637 |
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author | Gu, Hao Wu, Wei Yuan, Beilei Tang, Qiuqin Guo, Dan Chen, Yiqiu Xia, Yankai Hu, Lingqing Chen, Daozhen Sha, Jiahao Wang, Xinru |
author_facet | Gu, Hao Wu, Wei Yuan, Beilei Tang, Qiuqin Guo, Dan Chen, Yiqiu Xia, Yankai Hu, Lingqing Chen, Daozhen Sha, Jiahao Wang, Xinru |
author_sort | Gu, Hao |
collection | PubMed |
description | Genistein (GEN) is one of the isoflavones that has effect on male reproduction. However, the underlying mechanism remains unknown. miRNAs are a type of small non-coding RNAs that play important roles in spermatogenesis. We measured the GEN levels and miR-17-92 cluster expression in infertile subjects and found that miR-17-92 might be involved in GEN induced abnormal spermatogenesis. To clarify, we fed adult ICR mice with different doses of GEN (0, 0.5, 5, 50 and 250 mg/kg/day) for 35 days to study the underlying mechanism. We found that sperm average path velocity, straight-line velocity and eurvilinear velocity of the mice orally with GEN at 5mg/kg/day were significantly decreased, the expression levels of miR-17 and miR-20a in mice testis were higher in corresponding group. We also found miR-20a was the only miRNA that differentially expressed both in human and mice. By applying bioinformatics methods, Limk1 was predicted to be the target gene of miR-20a that is involved in spermatogenesis. Limk1 were significantly decreased in the corresponding group. Dual-luciferase report assay also proved that miR-20a could directly target Limk1. These results implied that Limk1 might be the target gene of miR-20a that is involved in GEN induced abnormal spermatogenesis. |
format | Online Article Text |
id | pubmed-5601687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56016872017-09-21 Genistein up-regulates miR-20a to disrupt spermatogenesis via targeting Limk1 Gu, Hao Wu, Wei Yuan, Beilei Tang, Qiuqin Guo, Dan Chen, Yiqiu Xia, Yankai Hu, Lingqing Chen, Daozhen Sha, Jiahao Wang, Xinru Oncotarget Research Paper Genistein (GEN) is one of the isoflavones that has effect on male reproduction. However, the underlying mechanism remains unknown. miRNAs are a type of small non-coding RNAs that play important roles in spermatogenesis. We measured the GEN levels and miR-17-92 cluster expression in infertile subjects and found that miR-17-92 might be involved in GEN induced abnormal spermatogenesis. To clarify, we fed adult ICR mice with different doses of GEN (0, 0.5, 5, 50 and 250 mg/kg/day) for 35 days to study the underlying mechanism. We found that sperm average path velocity, straight-line velocity and eurvilinear velocity of the mice orally with GEN at 5mg/kg/day were significantly decreased, the expression levels of miR-17 and miR-20a in mice testis were higher in corresponding group. We also found miR-20a was the only miRNA that differentially expressed both in human and mice. By applying bioinformatics methods, Limk1 was predicted to be the target gene of miR-20a that is involved in spermatogenesis. Limk1 were significantly decreased in the corresponding group. Dual-luciferase report assay also proved that miR-20a could directly target Limk1. These results implied that Limk1 might be the target gene of miR-20a that is involved in GEN induced abnormal spermatogenesis. Impact Journals LLC 2017-05-05 /pmc/articles/PMC5601687/ /pubmed/28938591 http://dx.doi.org/10.18632/oncotarget.17637 Text en Copyright: © 2017 Gu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Gu, Hao Wu, Wei Yuan, Beilei Tang, Qiuqin Guo, Dan Chen, Yiqiu Xia, Yankai Hu, Lingqing Chen, Daozhen Sha, Jiahao Wang, Xinru Genistein up-regulates miR-20a to disrupt spermatogenesis via targeting Limk1 |
title | Genistein up-regulates miR-20a to disrupt spermatogenesis via targeting Limk1 |
title_full | Genistein up-regulates miR-20a to disrupt spermatogenesis via targeting Limk1 |
title_fullStr | Genistein up-regulates miR-20a to disrupt spermatogenesis via targeting Limk1 |
title_full_unstemmed | Genistein up-regulates miR-20a to disrupt spermatogenesis via targeting Limk1 |
title_short | Genistein up-regulates miR-20a to disrupt spermatogenesis via targeting Limk1 |
title_sort | genistein up-regulates mir-20a to disrupt spermatogenesis via targeting limk1 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601687/ https://www.ncbi.nlm.nih.gov/pubmed/28938591 http://dx.doi.org/10.18632/oncotarget.17637 |
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