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Heterozygous mutation of eEF1A1b resulted in spermatogenesis arrest and infertility in male tilapia, Oreochromis niloticus
Eukaryotic elongation factor 1 alpha (eEF1A) is an essential component of the translational apparatus. In the present study, eEF1A1b was isolated from the Nile tilapia. Real-time PCR and Western blot revealed that eEF1A1b was expressed highly in the testis from 90 dah (days after hatching) onwards....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339811/ https://www.ncbi.nlm.nih.gov/pubmed/28266557 http://dx.doi.org/10.1038/srep43733 |
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author | Chen, Jinlin Jiang, Dongneng Tan, Dejie Fan, Zheng Wei, Yingying Li, Minghui Wang, Deshou |
author_facet | Chen, Jinlin Jiang, Dongneng Tan, Dejie Fan, Zheng Wei, Yingying Li, Minghui Wang, Deshou |
author_sort | Chen, Jinlin |
collection | PubMed |
description | Eukaryotic elongation factor 1 alpha (eEF1A) is an essential component of the translational apparatus. In the present study, eEF1A1b was isolated from the Nile tilapia. Real-time PCR and Western blot revealed that eEF1A1b was expressed highly in the testis from 90 dah (days after hatching) onwards. In situ hybridization and immunohistochemistry analyses showed that eEF1A1b was highly expressed in the spermatogonia of the testis. CRISPR/Cas9 mediated mutation of eEF1A1b resulted in spermatogenesis arrest and infertility in the F(0) XY fish. Consistently, heterozygous mutation of eEF1A1b (eEF1A1b(+/−)) resulted in an absence of spermatocytes at 90 dah, very few spermatocytes, spermatids and spermatozoa at 180 dah, and decreased Cyp11b2 and serum 11-ketotestosterone level at both stages. Further examination of the fertilization capacity of the sperm indicated that the eEF1A1b(+/−) XY fish were infertile due to abnormal spermiogenesis. Transcriptomic analyses of the eEF1A1b(+/−) testis from 180 dah XY fish revealed that key elements involved in spermatogenesis, steroidogenesis and sperm motility were significantly down-regulated compared with the control XY. Transgenic overexpression of eEF1A1b rescued the spermatogenesis arrest phenotype of the eEF1A1b(+/−) testis. Taken together, our data suggested that eEF1A1b is crucial for spermatogenesis and male fertility in the Nile tilapia. |
format | Online Article Text |
id | pubmed-5339811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53398112017-03-10 Heterozygous mutation of eEF1A1b resulted in spermatogenesis arrest and infertility in male tilapia, Oreochromis niloticus Chen, Jinlin Jiang, Dongneng Tan, Dejie Fan, Zheng Wei, Yingying Li, Minghui Wang, Deshou Sci Rep Article Eukaryotic elongation factor 1 alpha (eEF1A) is an essential component of the translational apparatus. In the present study, eEF1A1b was isolated from the Nile tilapia. Real-time PCR and Western blot revealed that eEF1A1b was expressed highly in the testis from 90 dah (days after hatching) onwards. In situ hybridization and immunohistochemistry analyses showed that eEF1A1b was highly expressed in the spermatogonia of the testis. CRISPR/Cas9 mediated mutation of eEF1A1b resulted in spermatogenesis arrest and infertility in the F(0) XY fish. Consistently, heterozygous mutation of eEF1A1b (eEF1A1b(+/−)) resulted in an absence of spermatocytes at 90 dah, very few spermatocytes, spermatids and spermatozoa at 180 dah, and decreased Cyp11b2 and serum 11-ketotestosterone level at both stages. Further examination of the fertilization capacity of the sperm indicated that the eEF1A1b(+/−) XY fish were infertile due to abnormal spermiogenesis. Transcriptomic analyses of the eEF1A1b(+/−) testis from 180 dah XY fish revealed that key elements involved in spermatogenesis, steroidogenesis and sperm motility were significantly down-regulated compared with the control XY. Transgenic overexpression of eEF1A1b rescued the spermatogenesis arrest phenotype of the eEF1A1b(+/−) testis. Taken together, our data suggested that eEF1A1b is crucial for spermatogenesis and male fertility in the Nile tilapia. Nature Publishing Group 2017-03-07 /pmc/articles/PMC5339811/ /pubmed/28266557 http://dx.doi.org/10.1038/srep43733 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chen, Jinlin Jiang, Dongneng Tan, Dejie Fan, Zheng Wei, Yingying Li, Minghui Wang, Deshou Heterozygous mutation of eEF1A1b resulted in spermatogenesis arrest and infertility in male tilapia, Oreochromis niloticus |
title | Heterozygous mutation of eEF1A1b resulted in spermatogenesis arrest and infertility in male tilapia, Oreochromis niloticus |
title_full | Heterozygous mutation of eEF1A1b resulted in spermatogenesis arrest and infertility in male tilapia, Oreochromis niloticus |
title_fullStr | Heterozygous mutation of eEF1A1b resulted in spermatogenesis arrest and infertility in male tilapia, Oreochromis niloticus |
title_full_unstemmed | Heterozygous mutation of eEF1A1b resulted in spermatogenesis arrest and infertility in male tilapia, Oreochromis niloticus |
title_short | Heterozygous mutation of eEF1A1b resulted in spermatogenesis arrest and infertility in male tilapia, Oreochromis niloticus |
title_sort | heterozygous mutation of eef1a1b resulted in spermatogenesis arrest and infertility in male tilapia, oreochromis niloticus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339811/ https://www.ncbi.nlm.nih.gov/pubmed/28266557 http://dx.doi.org/10.1038/srep43733 |
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