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A vaccine grade of yeast Saccharomyces cerevisiae expressing mammalian myostatin
BACKGROUND: Yeast Saccharomyces cerevisiae is a widely-used system for protein expression. We previously showed that heat-killed whole recombinant yeast vaccine expressing mammalian myostatin can modulate myostatin function in mice, resulting in increase of body weight and muscle composition in thes...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543327/ https://www.ncbi.nlm.nih.gov/pubmed/23253888 http://dx.doi.org/10.1186/1472-6750-12-97 |
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author | Zhang, Tingting Sun, Lin Xin, Ying Ma, Lixia Zhang, Youyou Wang, Xin Xu, Kun Ren, Chonghua Zhang, Cunfang Chen, Zhilong Yang, Hanjiang Zhang, Zhiying |
author_facet | Zhang, Tingting Sun, Lin Xin, Ying Ma, Lixia Zhang, Youyou Wang, Xin Xu, Kun Ren, Chonghua Zhang, Cunfang Chen, Zhilong Yang, Hanjiang Zhang, Zhiying |
author_sort | Zhang, Tingting |
collection | PubMed |
description | BACKGROUND: Yeast Saccharomyces cerevisiae is a widely-used system for protein expression. We previously showed that heat-killed whole recombinant yeast vaccine expressing mammalian myostatin can modulate myostatin function in mice, resulting in increase of body weight and muscle composition in these animals. Foreign DNA introduced into yeast cells can be lost soon unless cells are continuously cultured in selection media, which usually contain antibiotics. For cost and safety concerns, it is essential to optimize conditions to produce quality food and pharmaceutical products. RESULTS: We developed a simple but effective method to engineer a yeast strain stably expressing mammalian myostatin. This method utilized high-copy-number integration of myostatin gene into the ribosomal DNA of Saccharomyces cerevisiae. In the final step, antibiotic selection marker was removed using the Cre-LoxP system to minimize any possible side-effects for animals. The resulting yeast strain can be maintained in rich culture media and stably express mammalian myostatin for two years. Oral administration of the recombinant yeast was able to induce immune response to myostatin and modulated the body weight of mice. CONCLUSIONS: Establishment of such yeast strain is a step further toward transformation of yeast cells into edible vaccine to improve meat production in farm animals and treat human muscle-wasting diseases in the future. |
format | Online Article Text |
id | pubmed-3543327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35433272013-01-14 A vaccine grade of yeast Saccharomyces cerevisiae expressing mammalian myostatin Zhang, Tingting Sun, Lin Xin, Ying Ma, Lixia Zhang, Youyou Wang, Xin Xu, Kun Ren, Chonghua Zhang, Cunfang Chen, Zhilong Yang, Hanjiang Zhang, Zhiying BMC Biotechnol Research Article BACKGROUND: Yeast Saccharomyces cerevisiae is a widely-used system for protein expression. We previously showed that heat-killed whole recombinant yeast vaccine expressing mammalian myostatin can modulate myostatin function in mice, resulting in increase of body weight and muscle composition in these animals. Foreign DNA introduced into yeast cells can be lost soon unless cells are continuously cultured in selection media, which usually contain antibiotics. For cost and safety concerns, it is essential to optimize conditions to produce quality food and pharmaceutical products. RESULTS: We developed a simple but effective method to engineer a yeast strain stably expressing mammalian myostatin. This method utilized high-copy-number integration of myostatin gene into the ribosomal DNA of Saccharomyces cerevisiae. In the final step, antibiotic selection marker was removed using the Cre-LoxP system to minimize any possible side-effects for animals. The resulting yeast strain can be maintained in rich culture media and stably express mammalian myostatin for two years. Oral administration of the recombinant yeast was able to induce immune response to myostatin and modulated the body weight of mice. CONCLUSIONS: Establishment of such yeast strain is a step further toward transformation of yeast cells into edible vaccine to improve meat production in farm animals and treat human muscle-wasting diseases in the future. BioMed Central 2012-12-19 /pmc/articles/PMC3543327/ /pubmed/23253888 http://dx.doi.org/10.1186/1472-6750-12-97 Text en Copyright ©2012 Zhang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhang, Tingting Sun, Lin Xin, Ying Ma, Lixia Zhang, Youyou Wang, Xin Xu, Kun Ren, Chonghua Zhang, Cunfang Chen, Zhilong Yang, Hanjiang Zhang, Zhiying A vaccine grade of yeast Saccharomyces cerevisiae expressing mammalian myostatin |
title | A vaccine grade of yeast Saccharomyces cerevisiae expressing mammalian myostatin |
title_full | A vaccine grade of yeast Saccharomyces cerevisiae expressing mammalian myostatin |
title_fullStr | A vaccine grade of yeast Saccharomyces cerevisiae expressing mammalian myostatin |
title_full_unstemmed | A vaccine grade of yeast Saccharomyces cerevisiae expressing mammalian myostatin |
title_short | A vaccine grade of yeast Saccharomyces cerevisiae expressing mammalian myostatin |
title_sort | vaccine grade of yeast saccharomyces cerevisiae expressing mammalian myostatin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543327/ https://www.ncbi.nlm.nih.gov/pubmed/23253888 http://dx.doi.org/10.1186/1472-6750-12-97 |
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