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Structural mutation affecting intracellular transport and cell surface expression of murine class II molecules

We have selected Ia variants from the Ia+ (H-2d) M12.4.1 B cell lymphoma that are negative on the cell surface for one or both Ia isotypes. The molecular analysis of two such independently selected cell lines, M12.A2 and M12.C3, is reported here. This analysis revealed that the genes encoding Ad bet...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188865/
https://www.ncbi.nlm.nih.gov/pubmed/3126253
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description We have selected Ia variants from the Ia+ (H-2d) M12.4.1 B cell lymphoma that are negative on the cell surface for one or both Ia isotypes. The molecular analysis of two such independently selected cell lines, M12.A2 and M12.C3, is reported here. This analysis revealed that the genes encoding Ad beta (M12.A2) and Ed beta (M12.C3) contained identical single-nucleotide transitions that resulted in the substitution of Ser (mutant) for Asn (wild-type) at residue 82/83 of the extracellular NH2-terminal (membrane distal) beta 1 domain. This conservative substitution caused a cytoplasmic accumulation of I-A or I- E molecules in the respective cell line although predicted secondary- structure analysis suggests a minimal effect on protein conformation. Thus, the mutation appears to have either created a negative signal that stops transport or eliminated a positive signal that is required for transport and targeting to the cell surface.
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spelling pubmed-21888652008-04-17 Structural mutation affecting intracellular transport and cell surface expression of murine class II molecules J Exp Med Articles We have selected Ia variants from the Ia+ (H-2d) M12.4.1 B cell lymphoma that are negative on the cell surface for one or both Ia isotypes. The molecular analysis of two such independently selected cell lines, M12.A2 and M12.C3, is reported here. This analysis revealed that the genes encoding Ad beta (M12.A2) and Ed beta (M12.C3) contained identical single-nucleotide transitions that resulted in the substitution of Ser (mutant) for Asn (wild-type) at residue 82/83 of the extracellular NH2-terminal (membrane distal) beta 1 domain. This conservative substitution caused a cytoplasmic accumulation of I-A or I- E molecules in the respective cell line although predicted secondary- structure analysis suggests a minimal effect on protein conformation. Thus, the mutation appears to have either created a negative signal that stops transport or eliminated a positive signal that is required for transport and targeting to the cell surface. The Rockefeller University Press 1988-02-01 /pmc/articles/PMC2188865/ /pubmed/3126253 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
Structural mutation affecting intracellular transport and cell surface expression of murine class II molecules
title Structural mutation affecting intracellular transport and cell surface expression of murine class II molecules
title_full Structural mutation affecting intracellular transport and cell surface expression of murine class II molecules
title_fullStr Structural mutation affecting intracellular transport and cell surface expression of murine class II molecules
title_full_unstemmed Structural mutation affecting intracellular transport and cell surface expression of murine class II molecules
title_short Structural mutation affecting intracellular transport and cell surface expression of murine class II molecules
title_sort structural mutation affecting intracellular transport and cell surface expression of murine class ii molecules
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188865/
https://www.ncbi.nlm.nih.gov/pubmed/3126253