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INHERITANCE OF ANTIBODY SPECIFICITY : I. Anti-(4-Hydroxy-3-Nitrophenyl)Acetyl of the Mouse Primary Response
Our data suggest that fine specificity of antihapten antibodies is a useful Mendelian marker of variable (V) genes. We found that some mouse strains (e.g., C57/BL6) consistently produced heteroclitic anti-(4-hydroxy-3-nitrophenyl)acetyl (NP) antibodies (relative affinity for related (4-hydroxy-5-iod...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1974
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139760/ https://www.ncbi.nlm.nih.gov/pubmed/4139230 |
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author | Imanishi, Thereza Mäkelä, O. |
author_facet | Imanishi, Thereza Mäkelä, O. |
author_sort | Imanishi, Thereza |
collection | PubMed |
description | Our data suggest that fine specificity of antihapten antibodies is a useful Mendelian marker of variable (V) genes. We found that some mouse strains (e.g., C57/BL6) consistently produced heteroclitic anti-(4-hydroxy-3-nitrophenyl)acetyl (NP) antibodies (relative affinity for related (4-hydroxy-5-iodo-3-nitrophenyl)acetyl and (4-hydroxy-3.5-dinitrophenyl)acetyl was always >2) while other strains (e.g., CBA) produced "conventional" anti-NP antibodies (relative affinities were consistently <1). 48 (CBA x C57BL/6)F(1) mice were studied and most of them had heteroclitic anti-NP antibodies. They were backcrossed to the recessive CBA parent, and 87 backcross animals were similarly tested. Those heterozygous for the C57BL/6 heavy (H)-chain allotype were similar to the C57BL/6 and the F(1) mice while mice homozygous for the CBA allotype were indistinguishable from the CBA. Such monogenic inheritance was observed only in the primary response. Predominance of allotype-linked genes in the control of the fine specificity characteristics was confirmed by immunizing selected homozygous mouse strains. These mice contained various mixtures of genes from C57BL, BALB/c, and other strains. Specificity of their anti-NP was exclusively determined by genes linked to the H-chain allotype, no influence could be attributed to other genes including the H-2-linked genes. |
format | Text |
id | pubmed-2139760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1974 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21397602008-04-17 INHERITANCE OF ANTIBODY SPECIFICITY : I. Anti-(4-Hydroxy-3-Nitrophenyl)Acetyl of the Mouse Primary Response Imanishi, Thereza Mäkelä, O. J Exp Med Article Our data suggest that fine specificity of antihapten antibodies is a useful Mendelian marker of variable (V) genes. We found that some mouse strains (e.g., C57/BL6) consistently produced heteroclitic anti-(4-hydroxy-3-nitrophenyl)acetyl (NP) antibodies (relative affinity for related (4-hydroxy-5-iodo-3-nitrophenyl)acetyl and (4-hydroxy-3.5-dinitrophenyl)acetyl was always >2) while other strains (e.g., CBA) produced "conventional" anti-NP antibodies (relative affinities were consistently <1). 48 (CBA x C57BL/6)F(1) mice were studied and most of them had heteroclitic anti-NP antibodies. They were backcrossed to the recessive CBA parent, and 87 backcross animals were similarly tested. Those heterozygous for the C57BL/6 heavy (H)-chain allotype were similar to the C57BL/6 and the F(1) mice while mice homozygous for the CBA allotype were indistinguishable from the CBA. Such monogenic inheritance was observed only in the primary response. Predominance of allotype-linked genes in the control of the fine specificity characteristics was confirmed by immunizing selected homozygous mouse strains. These mice contained various mixtures of genes from C57BL, BALB/c, and other strains. Specificity of their anti-NP was exclusively determined by genes linked to the H-chain allotype, no influence could be attributed to other genes including the H-2-linked genes. The Rockefeller University Press 1974-11-30 /pmc/articles/PMC2139760/ /pubmed/4139230 Text en Copyright © 1974 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 Imanishi, Thereza Mäkelä, O. INHERITANCE OF ANTIBODY SPECIFICITY : I. Anti-(4-Hydroxy-3-Nitrophenyl)Acetyl of the Mouse Primary Response |
title | INHERITANCE OF ANTIBODY SPECIFICITY : I. Anti-(4-Hydroxy-3-Nitrophenyl)Acetyl of the Mouse Primary Response |
title_full | INHERITANCE OF ANTIBODY SPECIFICITY : I. Anti-(4-Hydroxy-3-Nitrophenyl)Acetyl of the Mouse Primary Response |
title_fullStr | INHERITANCE OF ANTIBODY SPECIFICITY : I. Anti-(4-Hydroxy-3-Nitrophenyl)Acetyl of the Mouse Primary Response |
title_full_unstemmed | INHERITANCE OF ANTIBODY SPECIFICITY : I. Anti-(4-Hydroxy-3-Nitrophenyl)Acetyl of the Mouse Primary Response |
title_short | INHERITANCE OF ANTIBODY SPECIFICITY : I. Anti-(4-Hydroxy-3-Nitrophenyl)Acetyl of the Mouse Primary Response |
title_sort | inheritance of antibody specificity : i. anti-(4-hydroxy-3-nitrophenyl)acetyl of the mouse primary response |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139760/ https://www.ncbi.nlm.nih.gov/pubmed/4139230 |
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