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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....

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Autores principales: Chen, Jinlin, Jiang, Dongneng, Tan, Dejie, Fan, Zheng, Wei, Yingying, Li, Minghui, Wang, Deshou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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.
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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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