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Replication and transcription of human papillomavirus type 58 genome in Saccharomyces cerevisiae

BACKGROUND: To establish a convenient system for the study of human papillomavirus (HPV), we inserted a Saccharomyces cerevisiae selectable marker, Ura, into HPV58 genome and transformed it into yeast. RESULTS: HPV58 genome could replicate extrachromosomally in yeast, with transcription of its early...

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Detalles Bibliográficos
Autores principales: Li, Jing, Wang, Xiao, Liu, Juan, Wang, Hong, Zhang, Xiao-Li, Tang, Wei, Sun, Yun-Dong, Wang, Xin, Yu, Xiu-Ping, Zhao, Wei-Ming
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3016283/
https://www.ncbi.nlm.nih.gov/pubmed/21156081
http://dx.doi.org/10.1186/1743-422X-7-368
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author Li, Jing
Wang, Xiao
Liu, Juan
Wang, Hong
Zhang, Xiao-Li
Tang, Wei
Sun, Yun-Dong
Wang, Xin
Yu, Xiu-Ping
Zhao, Wei-Ming
author_facet Li, Jing
Wang, Xiao
Liu, Juan
Wang, Hong
Zhang, Xiao-Li
Tang, Wei
Sun, Yun-Dong
Wang, Xin
Yu, Xiu-Ping
Zhao, Wei-Ming
author_sort Li, Jing
collection PubMed
description BACKGROUND: To establish a convenient system for the study of human papillomavirus (HPV), we inserted a Saccharomyces cerevisiae selectable marker, Ura, into HPV58 genome and transformed it into yeast. RESULTS: HPV58 genome could replicate extrachromosomally in yeast, with transcription of its early and late genes. However, with mutation of the viral E2 gene, HPV58 genome lost its mitotic stability, and the transcription levels of E6 and E7 genes were upregulated. CONCLUSIONS: E2 protein could participate in viral genome maintenance, replication and transcription regulation. This yeast model could be used for the study of certain aspects of HPV life cycle.
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spelling pubmed-30162832011-01-06 Replication and transcription of human papillomavirus type 58 genome in Saccharomyces cerevisiae Li, Jing Wang, Xiao Liu, Juan Wang, Hong Zhang, Xiao-Li Tang, Wei Sun, Yun-Dong Wang, Xin Yu, Xiu-Ping Zhao, Wei-Ming Virol J Research BACKGROUND: To establish a convenient system for the study of human papillomavirus (HPV), we inserted a Saccharomyces cerevisiae selectable marker, Ura, into HPV58 genome and transformed it into yeast. RESULTS: HPV58 genome could replicate extrachromosomally in yeast, with transcription of its early and late genes. However, with mutation of the viral E2 gene, HPV58 genome lost its mitotic stability, and the transcription levels of E6 and E7 genes were upregulated. CONCLUSIONS: E2 protein could participate in viral genome maintenance, replication and transcription regulation. This yeast model could be used for the study of certain aspects of HPV life cycle. BioMed Central 2010-12-15 /pmc/articles/PMC3016283/ /pubmed/21156081 http://dx.doi.org/10.1186/1743-422X-7-368 Text en Copyright ©2010 Li et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Li, Jing
Wang, Xiao
Liu, Juan
Wang, Hong
Zhang, Xiao-Li
Tang, Wei
Sun, Yun-Dong
Wang, Xin
Yu, Xiu-Ping
Zhao, Wei-Ming
Replication and transcription of human papillomavirus type 58 genome in Saccharomyces cerevisiae
title Replication and transcription of human papillomavirus type 58 genome in Saccharomyces cerevisiae
title_full Replication and transcription of human papillomavirus type 58 genome in Saccharomyces cerevisiae
title_fullStr Replication and transcription of human papillomavirus type 58 genome in Saccharomyces cerevisiae
title_full_unstemmed Replication and transcription of human papillomavirus type 58 genome in Saccharomyces cerevisiae
title_short Replication and transcription of human papillomavirus type 58 genome in Saccharomyces cerevisiae
title_sort replication and transcription of human papillomavirus type 58 genome in saccharomyces cerevisiae
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3016283/
https://www.ncbi.nlm.nih.gov/pubmed/21156081
http://dx.doi.org/10.1186/1743-422X-7-368
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