Cargando…
The immune response of allophenic mice to the synthetic polymer L-glutamic acid, L-lysine, L-phenylalanine. II. Lack of gene complementation in two nonresponder strains
The genetic control of the immune response of inbred strains of mice to certain antigens has been demonstrated to be governed by a set of Ir genes linked to the major histocompatibility complex (H-2) of mice (1,2). Until recently, the control was thought to be governed by single, dominant genes, loc...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1977
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180709/ https://www.ncbi.nlm.nih.gov/pubmed/233915 |
_version_ | 1782145609899180032 |
---|---|
author | Warner, CM McIvor, JL Maurer, PH Merryman, CF |
author_facet | Warner, CM McIvor, JL Maurer, PH Merryman, CF |
author_sort | Warner, CM |
collection | PubMed |
description | The genetic control of the immune response of inbred strains of mice to certain antigens has been demonstrated to be governed by a set of Ir genes linked to the major histocompatibility complex (H-2) of mice (1,2). Until recently, the control was thought to be governed by single, dominant genes, located within the I region of the H-2 complex. Merryman et al. (3) originally demonstrated that the immune response to the synthetic terpolymer L-glutamic acid, L-lysine, L-phenylaline (GLφ) is under dominant, H-2-linked Ir gene control (4-7). This was shown both by crossing two nonresponder parental strains to produce responder offspring in the F(1) generation, and by the analysis of appropriate recombinant stains of mice. The two complementing genes have been mapped in the IA and IC regions of the H-2 complex, and have been termed β and α, respectively (5,6). Thus, any strain of mouse may contain neither, one, or both genes. Only mice containing both genes are capable of responding to GLφ. It has been shown using F(1) hybrid and recombinant strains of mice, that the α- and β-genes can complement each other in either the cis (on the same chromosome) or in the trans (on different chromosomes) position (8). In this paper we report the results of studies aimed at answering the question of whether or not the α- and β- genes can complement each other when they are present in different lymphoid cells. To this end we have constructed allophenic mice composed of two nonresponder strains (A and C57BL/6), which show gene complementation in the F(1) generation. Allophenic mice are chimeras containing two cell types coexisting in a “normal” environment. The mice were tested for the specific cellular composition of the two parental cell types and were found to possess a complete range in the relative proportion of the two cell types. This report demonstrates that regardless of the mixture of cell types present in the allophenic mice, none of them were responders to GLφ. Thus no complementation of the α- and β-genes is seen when the two genes are present in different cells. |
format | Text |
id | pubmed-2180709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1977 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21807092008-04-17 The immune response of allophenic mice to the synthetic polymer L-glutamic acid, L-lysine, L-phenylalanine. II. Lack of gene complementation in two nonresponder strains Warner, CM McIvor, JL Maurer, PH Merryman, CF J Exp Med Articles The genetic control of the immune response of inbred strains of mice to certain antigens has been demonstrated to be governed by a set of Ir genes linked to the major histocompatibility complex (H-2) of mice (1,2). Until recently, the control was thought to be governed by single, dominant genes, located within the I region of the H-2 complex. Merryman et al. (3) originally demonstrated that the immune response to the synthetic terpolymer L-glutamic acid, L-lysine, L-phenylaline (GLφ) is under dominant, H-2-linked Ir gene control (4-7). This was shown both by crossing two nonresponder parental strains to produce responder offspring in the F(1) generation, and by the analysis of appropriate recombinant stains of mice. The two complementing genes have been mapped in the IA and IC regions of the H-2 complex, and have been termed β and α, respectively (5,6). Thus, any strain of mouse may contain neither, one, or both genes. Only mice containing both genes are capable of responding to GLφ. It has been shown using F(1) hybrid and recombinant strains of mice, that the α- and β-genes can complement each other in either the cis (on the same chromosome) or in the trans (on different chromosomes) position (8). In this paper we report the results of studies aimed at answering the question of whether or not the α- and β- genes can complement each other when they are present in different lymphoid cells. To this end we have constructed allophenic mice composed of two nonresponder strains (A and C57BL/6), which show gene complementation in the F(1) generation. Allophenic mice are chimeras containing two cell types coexisting in a “normal” environment. The mice were tested for the specific cellular composition of the two parental cell types and were found to possess a complete range in the relative proportion of the two cell types. This report demonstrates that regardless of the mixture of cell types present in the allophenic mice, none of them were responders to GLφ. Thus no complementation of the α- and β-genes is seen when the two genes are present in different cells. The Rockefeller University Press 1977-03-01 /pmc/articles/PMC2180709/ /pubmed/233915 Text en 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 | Articles Warner, CM McIvor, JL Maurer, PH Merryman, CF The immune response of allophenic mice to the synthetic polymer L-glutamic acid, L-lysine, L-phenylalanine. II. Lack of gene complementation in two nonresponder strains |
title | The immune response of allophenic mice to the synthetic polymer L-glutamic acid, L-lysine, L-phenylalanine. II. Lack of gene complementation in two nonresponder strains |
title_full | The immune response of allophenic mice to the synthetic polymer L-glutamic acid, L-lysine, L-phenylalanine. II. Lack of gene complementation in two nonresponder strains |
title_fullStr | The immune response of allophenic mice to the synthetic polymer L-glutamic acid, L-lysine, L-phenylalanine. II. Lack of gene complementation in two nonresponder strains |
title_full_unstemmed | The immune response of allophenic mice to the synthetic polymer L-glutamic acid, L-lysine, L-phenylalanine. II. Lack of gene complementation in two nonresponder strains |
title_short | The immune response of allophenic mice to the synthetic polymer L-glutamic acid, L-lysine, L-phenylalanine. II. Lack of gene complementation in two nonresponder strains |
title_sort | immune response of allophenic mice to the synthetic polymer l-glutamic acid, l-lysine, l-phenylalanine. ii. lack of gene complementation in two nonresponder strains |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180709/ https://www.ncbi.nlm.nih.gov/pubmed/233915 |
work_keys_str_mv | AT warnercm theimmuneresponseofallophenicmicetothesyntheticpolymerlglutamicacidllysinelphenylalanineiilackofgenecomplementationintwononresponderstrains AT mcivorjl theimmuneresponseofallophenicmicetothesyntheticpolymerlglutamicacidllysinelphenylalanineiilackofgenecomplementationintwononresponderstrains AT maurerph theimmuneresponseofallophenicmicetothesyntheticpolymerlglutamicacidllysinelphenylalanineiilackofgenecomplementationintwononresponderstrains AT merrymancf theimmuneresponseofallophenicmicetothesyntheticpolymerlglutamicacidllysinelphenylalanineiilackofgenecomplementationintwononresponderstrains AT warnercm immuneresponseofallophenicmicetothesyntheticpolymerlglutamicacidllysinelphenylalanineiilackofgenecomplementationintwononresponderstrains AT mcivorjl immuneresponseofallophenicmicetothesyntheticpolymerlglutamicacidllysinelphenylalanineiilackofgenecomplementationintwononresponderstrains AT maurerph immuneresponseofallophenicmicetothesyntheticpolymerlglutamicacidllysinelphenylalanineiilackofgenecomplementationintwononresponderstrains AT merrymancf immuneresponseofallophenicmicetothesyntheticpolymerlglutamicacidllysinelphenylalanineiilackofgenecomplementationintwononresponderstrains |