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GP73, a novel Golgi-localized protein upregulated by viral infection

We report the isolation and characterization of GP73, a novel 73 kDa human Golgi protein. The GP73 cDNA was cloned by differential screening of a cDNA library derived from the liver of a patient with adult giant-cell hepatitis (GCH), a rare form of hepatitis with presumed viral etiology. In vitro tr...

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Detalles Bibliográficos
Autores principales: Kladney, Raleigh D., Bulla, Gary A., Guo, Linsheng, Mason, Andrew L., Tollefson, Ann E., Simon, Daniela J., Koutoubi, Zaher, Fimmel, Claus J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science B.V. 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127640/
https://www.ncbi.nlm.nih.gov/pubmed/10831838
http://dx.doi.org/10.1016/S0378-1119(00)00136-0
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author Kladney, Raleigh D.
Bulla, Gary A.
Guo, Linsheng
Mason, Andrew L.
Tollefson, Ann E.
Simon, Daniela J.
Koutoubi, Zaher
Fimmel, Claus J.
author_facet Kladney, Raleigh D.
Bulla, Gary A.
Guo, Linsheng
Mason, Andrew L.
Tollefson, Ann E.
Simon, Daniela J.
Koutoubi, Zaher
Fimmel, Claus J.
author_sort Kladney, Raleigh D.
collection PubMed
description We report the isolation and characterization of GP73, a novel 73 kDa human Golgi protein. The GP73 cDNA was cloned by differential screening of a cDNA library derived from the liver of a patient with adult giant-cell hepatitis (GCH), a rare form of hepatitis with presumed viral etiology. In vitro transcription–translation studies indicate that GP73 is an integral membrane protein, and immunolocalization experiments using epitope-tagged GP73 demonstrate that the protein is localized to the Golgi apparatus. Northern blot analysis of RNA from multiple human tissues reveals a single GP73 mRNA transcript with a size of approximately 3.0 kb. Immunohistochemical studies using rabbit polyclonal antisera directed against recombinant GP73 demonstrate that the protein is preferentially expressed by epithelial cells in many human tissues. In normal livers, GP73 is consistently present in biliary epithelial cells, whereas hepatocytes show little or no signal. In contrast, livers of patients with GCH display strong GP73 immunoreactivity in multinucleated hepatocytes. GP73 mRNA and protein are expressed in highly differentiated HepG2 hepatoma cells after infection with adenovirus in vitro. We conclude that GP73 represents a novel, epithelial cell-specific integral membrane Golgi protein that can be upregulated in response to viral infection.
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spelling pubmed-71276402020-04-08 GP73, a novel Golgi-localized protein upregulated by viral infection Kladney, Raleigh D. Bulla, Gary A. Guo, Linsheng Mason, Andrew L. Tollefson, Ann E. Simon, Daniela J. Koutoubi, Zaher Fimmel, Claus J. Gene Article We report the isolation and characterization of GP73, a novel 73 kDa human Golgi protein. The GP73 cDNA was cloned by differential screening of a cDNA library derived from the liver of a patient with adult giant-cell hepatitis (GCH), a rare form of hepatitis with presumed viral etiology. In vitro transcription–translation studies indicate that GP73 is an integral membrane protein, and immunolocalization experiments using epitope-tagged GP73 demonstrate that the protein is localized to the Golgi apparatus. Northern blot analysis of RNA from multiple human tissues reveals a single GP73 mRNA transcript with a size of approximately 3.0 kb. Immunohistochemical studies using rabbit polyclonal antisera directed against recombinant GP73 demonstrate that the protein is preferentially expressed by epithelial cells in many human tissues. In normal livers, GP73 is consistently present in biliary epithelial cells, whereas hepatocytes show little or no signal. In contrast, livers of patients with GCH display strong GP73 immunoreactivity in multinucleated hepatocytes. GP73 mRNA and protein are expressed in highly differentiated HepG2 hepatoma cells after infection with adenovirus in vitro. We conclude that GP73 represents a novel, epithelial cell-specific integral membrane Golgi protein that can be upregulated in response to viral infection. Elsevier Science B.V. 2000-05-16 2000-05-18 /pmc/articles/PMC7127640/ /pubmed/10831838 http://dx.doi.org/10.1016/S0378-1119(00)00136-0 Text en Copyright © 2000 Elsevier Science B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Kladney, Raleigh D.
Bulla, Gary A.
Guo, Linsheng
Mason, Andrew L.
Tollefson, Ann E.
Simon, Daniela J.
Koutoubi, Zaher
Fimmel, Claus J.
GP73, a novel Golgi-localized protein upregulated by viral infection
title GP73, a novel Golgi-localized protein upregulated by viral infection
title_full GP73, a novel Golgi-localized protein upregulated by viral infection
title_fullStr GP73, a novel Golgi-localized protein upregulated by viral infection
title_full_unstemmed GP73, a novel Golgi-localized protein upregulated by viral infection
title_short GP73, a novel Golgi-localized protein upregulated by viral infection
title_sort gp73, a novel golgi-localized protein upregulated by viral infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127640/
https://www.ncbi.nlm.nih.gov/pubmed/10831838
http://dx.doi.org/10.1016/S0378-1119(00)00136-0
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