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Intratesticular injection followed by electroporation allows gene transfer in caprine spermatogenic cells

The production of transgenic livestock is constrained due to the limited success of currently available methods for transgenesis. Testis mediated gene transfer (TMGT) is an emerging method that shows a high success rate in generating transgenic mice. In this study, we report a newly developed protoc...

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Autores principales: Pramod, R. Kumar, Mitra, Abhijit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816633/
https://www.ncbi.nlm.nih.gov/pubmed/29453369
http://dx.doi.org/10.1038/s41598-018-21558-9
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author Pramod, R. Kumar
Mitra, Abhijit
author_facet Pramod, R. Kumar
Mitra, Abhijit
author_sort Pramod, R. Kumar
collection PubMed
description The production of transgenic livestock is constrained due to the limited success of currently available methods for transgenesis. Testis mediated gene transfer (TMGT) is an emerging method that shows a high success rate in generating transgenic mice. In this study, we report a newly developed protocol for electroporation-aided TMGT to produce a transgenic goat. The injectable volume and concentration of the transgene were first standardized, and then electroporation conditions were optimized in vitro. In vivo experiments were performed by injecting a transgenic construct (pIRES2-EGFP; enhanced green fluorescent protein) into the testicular interstitium followed by electroporation. Immunohistochemistry, quantitative real-time PCR (qPCR) and western blotting analyses confirmed the successful transfer of the transgene into seminiferous tubules and testicular cells. Furthermore, chromosomal integration of the transgene and its expression in sperm were evaluated d60 and d120 post-electroporation. Our protocol neither altered the seminal characteristics nor the fertilization capacity of the sperm cells. In vitro fertilization using transgenic sperm generated fluorescent embryos. Finally, natural mating of a pre-founder buck produced a transgenic baby goat. The present study demonstrates the first successful report of an electroporation-aided TMGT method for gene transfer in goats.
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spelling pubmed-58166332018-02-21 Intratesticular injection followed by electroporation allows gene transfer in caprine spermatogenic cells Pramod, R. Kumar Mitra, Abhijit Sci Rep Article The production of transgenic livestock is constrained due to the limited success of currently available methods for transgenesis. Testis mediated gene transfer (TMGT) is an emerging method that shows a high success rate in generating transgenic mice. In this study, we report a newly developed protocol for electroporation-aided TMGT to produce a transgenic goat. The injectable volume and concentration of the transgene were first standardized, and then electroporation conditions were optimized in vitro. In vivo experiments were performed by injecting a transgenic construct (pIRES2-EGFP; enhanced green fluorescent protein) into the testicular interstitium followed by electroporation. Immunohistochemistry, quantitative real-time PCR (qPCR) and western blotting analyses confirmed the successful transfer of the transgene into seminiferous tubules and testicular cells. Furthermore, chromosomal integration of the transgene and its expression in sperm were evaluated d60 and d120 post-electroporation. Our protocol neither altered the seminal characteristics nor the fertilization capacity of the sperm cells. In vitro fertilization using transgenic sperm generated fluorescent embryos. Finally, natural mating of a pre-founder buck produced a transgenic baby goat. The present study demonstrates the first successful report of an electroporation-aided TMGT method for gene transfer in goats. Nature Publishing Group UK 2018-02-16 /pmc/articles/PMC5816633/ /pubmed/29453369 http://dx.doi.org/10.1038/s41598-018-21558-9 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pramod, R. Kumar
Mitra, Abhijit
Intratesticular injection followed by electroporation allows gene transfer in caprine spermatogenic cells
title Intratesticular injection followed by electroporation allows gene transfer in caprine spermatogenic cells
title_full Intratesticular injection followed by electroporation allows gene transfer in caprine spermatogenic cells
title_fullStr Intratesticular injection followed by electroporation allows gene transfer in caprine spermatogenic cells
title_full_unstemmed Intratesticular injection followed by electroporation allows gene transfer in caprine spermatogenic cells
title_short Intratesticular injection followed by electroporation allows gene transfer in caprine spermatogenic cells
title_sort intratesticular injection followed by electroporation allows gene transfer in caprine spermatogenic cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816633/
https://www.ncbi.nlm.nih.gov/pubmed/29453369
http://dx.doi.org/10.1038/s41598-018-21558-9
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