Click R E, Cahill G, Schneider D, Adelmann A, Azar M M, Tarquinio J J, Peck A B
J Immunol. 1987 Jul 15;139(2):321-5.
Neither the biological function nor a basic understanding of the enigmatic chromosome 1-encoded Mls locus of the mouse has yet been uncovered despite extensive investigations. The present report is a continuation of our genetic analyses of the Mls locus in an attempt to better define the system. Data presented here indicate that in contrast to cells of mice expressing either the Mlsa or Mlsc allele which respond in mixed leukocyte reactions to cells expressing the Mlsd allelic products, cells from (Mlsa X Mlsc)F1-hybrid mice do not. In addition, the nonresponder phenotype appears to segregate as a single autosomal genetic system in backcross animals. These findings fail to support two recently advanced hypotheses: first, that the Mls locus is nonpolymorphic, or second, that the Mls locus controls differential expression of Ia antigenic determinants. Although the mechanism by which a (responder X responder) converts to a nonresponder remains unknown, three models involving gene complementation are discussed.
尽管进行了广泛研究,但小鼠1号染色体编码的神秘Mls基因座的生物学功能和基本认识仍未被揭示。本报告是我们对Mls基因座进行遗传分析的延续,旨在更好地界定该系统。此处呈现的数据表明,与表达Mlsa或Mlsc等位基因的小鼠细胞在混合淋巴细胞反应中对表达Mlsd等位基因产物的细胞有反应不同,(Mlsa×Mlsc)F1杂交小鼠的细胞没有反应。此外,在回交动物中,无反应者表型似乎作为一个单一的常染色体遗传系统进行分离。这些发现不支持最近提出的两个假说:第一,Mls基因座是非多态性的;第二,Mls基因座控制Ia抗原决定簇的差异表达。尽管(反应者×反应者)转变为无反应者的机制仍然未知,但讨论了三种涉及基因互补的模型。