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H-2-LINKED IMMUNE RESPONSE (Ir) GENES : INDEPENDENT LOCI FORIr-IgGANDIr-IgA GENES

Two H-2-linked autosomal dominant immune response (Ir) genes Ir-IgG and Ir-IgA were demonstrated to be at separate loci. Ir-IgG controls the immune response to IgG (γ2a) myeloma proteins and Ir-IgA the immune response to IgA meyloma proteins. Both genes are associated with the H-2K region specificit...

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Detalles Bibliográficos
Autores principales: Lieberman, R., Paul, W. E., Humphrey, W., Stimpfling, J. H.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1972
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139291/
https://www.ncbi.nlm.nih.gov/pubmed/4117190
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author Lieberman, R.
Paul, W. E.
Humphrey, W.
Stimpfling, J. H.
author_facet Lieberman, R.
Paul, W. E.
Humphrey, W.
Stimpfling, J. H.
author_sort Lieberman, R.
collection PubMed
description Two H-2-linked autosomal dominant immune response (Ir) genes Ir-IgG and Ir-IgA were demonstrated to be at separate loci. Ir-IgG controls the immune response to IgG (γ2a) myeloma proteins and Ir-IgA the immune response to IgA meyloma proteins. Both genes are associated with the H-2K region specificities of the H-2 chromosome, specifically Ir-IgG with H-2(b) and Ir-IgA with H-2(a). Different recombinants derived from H-2(a)/H-2(b) crossovers were examined for their immune responsiveness to BALB/c IgG (γ2a) and IgA myeloma proteins. B10 (H-2(b)) parental type responded only to IgG; B10.A (H-2(a)) responded only to IgA. All the recombinants except for B10.A (4R) responded to either IgG or IgA. B10.A (4R), however, responded to both IgG and IgA. This indicated that the crossover event giving rise to B10.A (4R) occurred between the Ir-IgG and Ir-IgA loci.
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spelling pubmed-21392912008-04-17 H-2-LINKED IMMUNE RESPONSE (Ir) GENES : INDEPENDENT LOCI FORIr-IgGANDIr-IgA GENES Lieberman, R. Paul, W. E. Humphrey, W. Stimpfling, J. H. J Exp Med Article Two H-2-linked autosomal dominant immune response (Ir) genes Ir-IgG and Ir-IgA were demonstrated to be at separate loci. Ir-IgG controls the immune response to IgG (γ2a) myeloma proteins and Ir-IgA the immune response to IgA meyloma proteins. Both genes are associated with the H-2K region specificities of the H-2 chromosome, specifically Ir-IgG with H-2(b) and Ir-IgA with H-2(a). Different recombinants derived from H-2(a)/H-2(b) crossovers were examined for their immune responsiveness to BALB/c IgG (γ2a) and IgA myeloma proteins. B10 (H-2(b)) parental type responded only to IgG; B10.A (H-2(a)) responded only to IgA. All the recombinants except for B10.A (4R) responded to either IgG or IgA. B10.A (4R), however, responded to both IgG and IgA. This indicated that the crossover event giving rise to B10.A (4R) occurred between the Ir-IgG and Ir-IgA loci. The Rockefeller University Press 1972-10-31 /pmc/articles/PMC2139291/ /pubmed/4117190 Text en Copyright © 1972 by 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
Lieberman, R.
Paul, W. E.
Humphrey, W.
Stimpfling, J. H.
H-2-LINKED IMMUNE RESPONSE (Ir) GENES : INDEPENDENT LOCI FORIr-IgGANDIr-IgA GENES
title H-2-LINKED IMMUNE RESPONSE (Ir) GENES : INDEPENDENT LOCI FORIr-IgGANDIr-IgA GENES
title_full H-2-LINKED IMMUNE RESPONSE (Ir) GENES : INDEPENDENT LOCI FORIr-IgGANDIr-IgA GENES
title_fullStr H-2-LINKED IMMUNE RESPONSE (Ir) GENES : INDEPENDENT LOCI FORIr-IgGANDIr-IgA GENES
title_full_unstemmed H-2-LINKED IMMUNE RESPONSE (Ir) GENES : INDEPENDENT LOCI FORIr-IgGANDIr-IgA GENES
title_short H-2-LINKED IMMUNE RESPONSE (Ir) GENES : INDEPENDENT LOCI FORIr-IgGANDIr-IgA GENES
title_sort h-2-linked immune response (ir) genes : independent loci forir-iggandir-iga genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139291/
https://www.ncbi.nlm.nih.gov/pubmed/4117190
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