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Molecular characterization of duck enteritis virus CHv strain UL49.5 protein and its colocalization with glycoprotein M
The UL49.5 gene of most herpesviruses is conserved and encodes glycoprotein N. However, the UL49.5 protein of duck enteritis virus (DEV) (pUL49.5) has not been reported. In the current study, the DEV pUL49.5 gene was first subjected to molecular characterization. To verify the predicted intracellula...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society of Veterinary Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4178140/ https://www.ncbi.nlm.nih.gov/pubmed/24690604 http://dx.doi.org/10.4142/jvs.2014.15.3.389 |
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author | Lin, Meng Jia, Renyong Wang, Mingshu Gao, Xinghong Zhu, Dekang Chen, Shun Liu, Mafeng Yin, Zhongqiong Wang, Yin Chen, Xiaoyue Cheng, Anchun |
author_facet | Lin, Meng Jia, Renyong Wang, Mingshu Gao, Xinghong Zhu, Dekang Chen, Shun Liu, Mafeng Yin, Zhongqiong Wang, Yin Chen, Xiaoyue Cheng, Anchun |
author_sort | Lin, Meng |
collection | PubMed |
description | The UL49.5 gene of most herpesviruses is conserved and encodes glycoprotein N. However, the UL49.5 protein of duck enteritis virus (DEV) (pUL49.5) has not been reported. In the current study, the DEV pUL49.5 gene was first subjected to molecular characterization. To verify the predicted intracellular localization of gene expression, the recombinant plasmid pEGFP-C1/pUL49.5 was constructed and used to transfect duck embryo fibroblasts. Next, the recombinant plasmid pDsRed1-N1/glycoprotein M (gM) was produced and used for co-transfection with the pEGFP-C1/pUL49.5 plasmid to determine whether DEV pUL49.5 and gM (a conserved protein in herpesviruses) colocalize. DEV pUL49.5 was thought to be an envelope glycoprotein with a signal peptide and two transmembrane domains. This protein was also predicted to localize in the cytoplasm and endoplasmic reticulum with a probability of 66.7%. Images taken by a fluorescence microscope at different time points revealed that the DEV pUL49.5 and gM proteins were both expressed in the cytoplasm. Overlap of the two different fluorescence signals appeared 12 h after transfection and continued to persist until the end of the experiment. These data indicate a possible interaction between DEV pUL49.5 and gM. |
format | Online Article Text |
id | pubmed-4178140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Korean Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41781402014-09-30 Molecular characterization of duck enteritis virus CHv strain UL49.5 protein and its colocalization with glycoprotein M Lin, Meng Jia, Renyong Wang, Mingshu Gao, Xinghong Zhu, Dekang Chen, Shun Liu, Mafeng Yin, Zhongqiong Wang, Yin Chen, Xiaoyue Cheng, Anchun J Vet Sci Original Article The UL49.5 gene of most herpesviruses is conserved and encodes glycoprotein N. However, the UL49.5 protein of duck enteritis virus (DEV) (pUL49.5) has not been reported. In the current study, the DEV pUL49.5 gene was first subjected to molecular characterization. To verify the predicted intracellular localization of gene expression, the recombinant plasmid pEGFP-C1/pUL49.5 was constructed and used to transfect duck embryo fibroblasts. Next, the recombinant plasmid pDsRed1-N1/glycoprotein M (gM) was produced and used for co-transfection with the pEGFP-C1/pUL49.5 plasmid to determine whether DEV pUL49.5 and gM (a conserved protein in herpesviruses) colocalize. DEV pUL49.5 was thought to be an envelope glycoprotein with a signal peptide and two transmembrane domains. This protein was also predicted to localize in the cytoplasm and endoplasmic reticulum with a probability of 66.7%. Images taken by a fluorescence microscope at different time points revealed that the DEV pUL49.5 and gM proteins were both expressed in the cytoplasm. Overlap of the two different fluorescence signals appeared 12 h after transfection and continued to persist until the end of the experiment. These data indicate a possible interaction between DEV pUL49.5 and gM. The Korean Society of Veterinary Science 2014-09 2014-09-16 /pmc/articles/PMC4178140/ /pubmed/24690604 http://dx.doi.org/10.4142/jvs.2014.15.3.389 Text en © 2014 The Korean Society of Veterinary Science. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lin, Meng Jia, Renyong Wang, Mingshu Gao, Xinghong Zhu, Dekang Chen, Shun Liu, Mafeng Yin, Zhongqiong Wang, Yin Chen, Xiaoyue Cheng, Anchun Molecular characterization of duck enteritis virus CHv strain UL49.5 protein and its colocalization with glycoprotein M |
title | Molecular characterization of duck enteritis virus CHv strain UL49.5 protein and its colocalization with glycoprotein M |
title_full | Molecular characterization of duck enteritis virus CHv strain UL49.5 protein and its colocalization with glycoprotein M |
title_fullStr | Molecular characterization of duck enteritis virus CHv strain UL49.5 protein and its colocalization with glycoprotein M |
title_full_unstemmed | Molecular characterization of duck enteritis virus CHv strain UL49.5 protein and its colocalization with glycoprotein M |
title_short | Molecular characterization of duck enteritis virus CHv strain UL49.5 protein and its colocalization with glycoprotein M |
title_sort | molecular characterization of duck enteritis virus chv strain ul49.5 protein and its colocalization with glycoprotein m |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4178140/ https://www.ncbi.nlm.nih.gov/pubmed/24690604 http://dx.doi.org/10.4142/jvs.2014.15.3.389 |
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