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Transgenic Expression of the Activating Natural Killer Receptor Ly49H Confers Resistance to Cytomegalovirus in Genetically Susceptible Mice

Natural resistance to infection with mouse cytomegalovirus (MCMV) is controlled by a dominant locus, Cmv1. Cmv1 is linked to the Ly49 family of natural killer receptors on distal chromosome 6. While some studies localized Cmv1 as distal to the Ly49 gene cluster, genetic and functional analysis ident...

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Autores principales: Lee, Seung-Hwan, Zafer, Ahmed, de Repentigny, Yves, Kothary, Rashmi, Tremblay, Michel L., Gros, Philippe, Duplay, Pascale, Webb, John R., Vidal, Silvia M.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193863/
https://www.ncbi.nlm.nih.gov/pubmed/12591908
http://dx.doi.org/10.1084/jem.20021713
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author Lee, Seung-Hwan
Zafer, Ahmed
de Repentigny, Yves
Kothary, Rashmi
Tremblay, Michel L.
Gros, Philippe
Duplay, Pascale
Webb, John R.
Vidal, Silvia M.
author_facet Lee, Seung-Hwan
Zafer, Ahmed
de Repentigny, Yves
Kothary, Rashmi
Tremblay, Michel L.
Gros, Philippe
Duplay, Pascale
Webb, John R.
Vidal, Silvia M.
author_sort Lee, Seung-Hwan
collection PubMed
description Natural resistance to infection with mouse cytomegalovirus (MCMV) is controlled by a dominant locus, Cmv1. Cmv1 is linked to the Ly49 family of natural killer receptors on distal chromosome 6. While some studies localized Cmv1 as distal to the Ly49 gene cluster, genetic and functional analysis identified Ly49h as a pivotal factor in resistance to MCMV. The role of these two independent genomic domains in MCMV resistance was evaluated by functional complementation using transgenesis of bacterial artificial chromosomes (BAC) in genetically susceptible mice. Phenotypic and genetic characterization of the transgenic animals traced the resistance gene to a single region spanning the Ly49h gene. The appearance of the Ly49H protein in NK cells of transgenic mice coincided with the emergence of MCMV resistance, and there was a threshold Ly49H protein level associated with full recovery. Finally, transgenic expression of Ly49H in the context of either of the two independent susceptibility alleles, Cmv1 (sBALB) or Cmv1 (sFVB), conferred resistance to MCMV infection. These results demonstrate that Ly49h is necessary and sufficient to confer MCMV resistance, and formally demonstrate allelism between Cmv1 and Ly49h. This panel of transgenic animals provides a unique resource to study possible pleiotropic effect of Cmv1.
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spelling pubmed-21938632008-04-11 Transgenic Expression of the Activating Natural Killer Receptor Ly49H Confers Resistance to Cytomegalovirus in Genetically Susceptible Mice Lee, Seung-Hwan Zafer, Ahmed de Repentigny, Yves Kothary, Rashmi Tremblay, Michel L. Gros, Philippe Duplay, Pascale Webb, John R. Vidal, Silvia M. J Exp Med Article Natural resistance to infection with mouse cytomegalovirus (MCMV) is controlled by a dominant locus, Cmv1. Cmv1 is linked to the Ly49 family of natural killer receptors on distal chromosome 6. While some studies localized Cmv1 as distal to the Ly49 gene cluster, genetic and functional analysis identified Ly49h as a pivotal factor in resistance to MCMV. The role of these two independent genomic domains in MCMV resistance was evaluated by functional complementation using transgenesis of bacterial artificial chromosomes (BAC) in genetically susceptible mice. Phenotypic and genetic characterization of the transgenic animals traced the resistance gene to a single region spanning the Ly49h gene. The appearance of the Ly49H protein in NK cells of transgenic mice coincided with the emergence of MCMV resistance, and there was a threshold Ly49H protein level associated with full recovery. Finally, transgenic expression of Ly49H in the context of either of the two independent susceptibility alleles, Cmv1 (sBALB) or Cmv1 (sFVB), conferred resistance to MCMV infection. These results demonstrate that Ly49h is necessary and sufficient to confer MCMV resistance, and formally demonstrate allelism between Cmv1 and Ly49h. This panel of transgenic animals provides a unique resource to study possible pleiotropic effect of Cmv1. The Rockefeller University Press 2003-02-17 /pmc/articles/PMC2193863/ /pubmed/12591908 http://dx.doi.org/10.1084/jem.20021713 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Lee, Seung-Hwan
Zafer, Ahmed
de Repentigny, Yves
Kothary, Rashmi
Tremblay, Michel L.
Gros, Philippe
Duplay, Pascale
Webb, John R.
Vidal, Silvia M.
Transgenic Expression of the Activating Natural Killer Receptor Ly49H Confers Resistance to Cytomegalovirus in Genetically Susceptible Mice
title Transgenic Expression of the Activating Natural Killer Receptor Ly49H Confers Resistance to Cytomegalovirus in Genetically Susceptible Mice
title_full Transgenic Expression of the Activating Natural Killer Receptor Ly49H Confers Resistance to Cytomegalovirus in Genetically Susceptible Mice
title_fullStr Transgenic Expression of the Activating Natural Killer Receptor Ly49H Confers Resistance to Cytomegalovirus in Genetically Susceptible Mice
title_full_unstemmed Transgenic Expression of the Activating Natural Killer Receptor Ly49H Confers Resistance to Cytomegalovirus in Genetically Susceptible Mice
title_short Transgenic Expression of the Activating Natural Killer Receptor Ly49H Confers Resistance to Cytomegalovirus in Genetically Susceptible Mice
title_sort transgenic expression of the activating natural killer receptor ly49h confers resistance to cytomegalovirus in genetically susceptible mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193863/
https://www.ncbi.nlm.nih.gov/pubmed/12591908
http://dx.doi.org/10.1084/jem.20021713
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