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Highly Efficient Generation of Transgenic Sheep by Lentivirus Accompanying the Alteration of Methylation Status

BACKGROUND: Low efficiency of gene transfer and silence of transgene expression are the critical factors hampering the development of transgenic livestock. Recently, transfer of recombinant lentivirus has been demonstrated to be an efficient transgene delivery method in various animals. However, the...

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Autores principales: Liu, Chenxi, Wang, Liqin, Li, Wenrong, Zhang, Xuemei, Tian, Yongzhi, Zhang, Ning, He, Sangang, Chen, Tong, Huang, Juncheng, Liu, Mingjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558511/
https://www.ncbi.nlm.nih.gov/pubmed/23382924
http://dx.doi.org/10.1371/journal.pone.0054614
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author Liu, Chenxi
Wang, Liqin
Li, Wenrong
Zhang, Xuemei
Tian, Yongzhi
Zhang, Ning
He, Sangang
Chen, Tong
Huang, Juncheng
Liu, Mingjun
author_facet Liu, Chenxi
Wang, Liqin
Li, Wenrong
Zhang, Xuemei
Tian, Yongzhi
Zhang, Ning
He, Sangang
Chen, Tong
Huang, Juncheng
Liu, Mingjun
author_sort Liu, Chenxi
collection PubMed
description BACKGROUND: Low efficiency of gene transfer and silence of transgene expression are the critical factors hampering the development of transgenic livestock. Recently, transfer of recombinant lentivirus has been demonstrated to be an efficient transgene delivery method in various animals. However, the lentiviral transgenesis and the methylation status of transgene in sheep have not been well addressed. METHODOLOGY/PRINCIPLE FINDINGS: EGFP transgenic sheep were generated by injecting recombinant lentivirus into zygotes. Of the 13 lambs born, 8 carried the EGFP transgene, and its chromosomal integration was identified in all tested tissues. Western blotting showed that GFP was expressed in all transgenic founders and their various tissues. Analysis of CpG methylation status of CMV promoter by bisulfate sequencing unraveled remarkable variation of methylation levels in transgenic sheep. The average methylation levels ranged from 37.6% to 79.1% in the transgenic individuals and 34.7% to 83% in the tested tissues. Correlative analysis of methylation status with GFP expression revealed that the GFP expression level was inversely correlated with methylation density. The similar phenomenon was also observed in tested tissues. Transgene integration determined by Southern blotting presented multiple integrants ranging from 2 to 6 copies in the genome of transgenic sheep. CONCLUSIONS/SIGNIFICANCE: Injection of lentiviral transgene into zygotes could be a promising efficient gene delivery system to generate transgenic sheep and achieved widespread transgene expression. The promoter of integrants transferred by lentiviral vector was subjected to dramatic alteration of methylation status and the transgene expression level was inversely correlative with promoter methylation density. Our work illustrated for the first time that generation of transgenic sheep by injecting recombinant lentivirus into zygote could be an efficient tool to improve sheep performance by genetic modification.
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spelling pubmed-35585112013-02-04 Highly Efficient Generation of Transgenic Sheep by Lentivirus Accompanying the Alteration of Methylation Status Liu, Chenxi Wang, Liqin Li, Wenrong Zhang, Xuemei Tian, Yongzhi Zhang, Ning He, Sangang Chen, Tong Huang, Juncheng Liu, Mingjun PLoS One Research Article BACKGROUND: Low efficiency of gene transfer and silence of transgene expression are the critical factors hampering the development of transgenic livestock. Recently, transfer of recombinant lentivirus has been demonstrated to be an efficient transgene delivery method in various animals. However, the lentiviral transgenesis and the methylation status of transgene in sheep have not been well addressed. METHODOLOGY/PRINCIPLE FINDINGS: EGFP transgenic sheep were generated by injecting recombinant lentivirus into zygotes. Of the 13 lambs born, 8 carried the EGFP transgene, and its chromosomal integration was identified in all tested tissues. Western blotting showed that GFP was expressed in all transgenic founders and their various tissues. Analysis of CpG methylation status of CMV promoter by bisulfate sequencing unraveled remarkable variation of methylation levels in transgenic sheep. The average methylation levels ranged from 37.6% to 79.1% in the transgenic individuals and 34.7% to 83% in the tested tissues. Correlative analysis of methylation status with GFP expression revealed that the GFP expression level was inversely correlated with methylation density. The similar phenomenon was also observed in tested tissues. Transgene integration determined by Southern blotting presented multiple integrants ranging from 2 to 6 copies in the genome of transgenic sheep. CONCLUSIONS/SIGNIFICANCE: Injection of lentiviral transgene into zygotes could be a promising efficient gene delivery system to generate transgenic sheep and achieved widespread transgene expression. The promoter of integrants transferred by lentiviral vector was subjected to dramatic alteration of methylation status and the transgene expression level was inversely correlative with promoter methylation density. Our work illustrated for the first time that generation of transgenic sheep by injecting recombinant lentivirus into zygote could be an efficient tool to improve sheep performance by genetic modification. Public Library of Science 2013-01-29 /pmc/articles/PMC3558511/ /pubmed/23382924 http://dx.doi.org/10.1371/journal.pone.0054614 Text en © 2013 Liu et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Liu, Chenxi
Wang, Liqin
Li, Wenrong
Zhang, Xuemei
Tian, Yongzhi
Zhang, Ning
He, Sangang
Chen, Tong
Huang, Juncheng
Liu, Mingjun
Highly Efficient Generation of Transgenic Sheep by Lentivirus Accompanying the Alteration of Methylation Status
title Highly Efficient Generation of Transgenic Sheep by Lentivirus Accompanying the Alteration of Methylation Status
title_full Highly Efficient Generation of Transgenic Sheep by Lentivirus Accompanying the Alteration of Methylation Status
title_fullStr Highly Efficient Generation of Transgenic Sheep by Lentivirus Accompanying the Alteration of Methylation Status
title_full_unstemmed Highly Efficient Generation of Transgenic Sheep by Lentivirus Accompanying the Alteration of Methylation Status
title_short Highly Efficient Generation of Transgenic Sheep by Lentivirus Accompanying the Alteration of Methylation Status
title_sort highly efficient generation of transgenic sheep by lentivirus accompanying the alteration of methylation status
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558511/
https://www.ncbi.nlm.nih.gov/pubmed/23382924
http://dx.doi.org/10.1371/journal.pone.0054614
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