Griffith I J, Nabavi N, Ghogawala Z, Chase C G, Rodriguez M, McKean D J, Glimcher L H
Department of Cancer Biology, Harvard School of Public Health, Boston, Massachusetts 02115.
J Exp Med. 1988 Feb 1;167(2):541-55. doi: 10.1084/jem.167.2.541.
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.
我们从Ia+(H-2d) M12.4.1 B细胞淋巴瘤中挑选出Ia变体,这些变体在细胞表面上对一种或两种Ia同种型呈阴性。本文报道了对两个如此独立挑选的细胞系M12.A2和M12.C3的分子分析。该分析表明,编码Ad beta(M12.A2)和Ed beta(M12.C3)的基因包含相同的单核苷酸转变,这导致在细胞外NH2末端(膜远端)β1结构域的第82/83位残基处,丝氨酸(突变型)取代了天冬酰胺(野生型)。这种保守性取代导致I-A或I-E分子在各自的细胞系中在细胞质中积累,尽管预测的二级结构分析表明对蛋白质构象的影响最小。因此,该突变似乎要么产生了一个阻止转运的负信号,要么消除了转运和靶向细胞表面所需的正信号。