Click R E, Adelmann A
Minnesota Heart Lung Institute, Department of Surgery and Microbiology, University of Minnesota, Minneapolis 55455.
Immunogenetics. 1989;29(3):155-60. doi: 10.1007/BF00373640.
Festenstein originally described the Mls locus as a single dominant autosomal gene with four alleles which mapped in the 13th linkage group of chromosome 1. We subsequently presented evidence indicating that the mixed leukocyte reaction (MLR) stimulatory products of DBA/2 and CBA/J were controlled by two independently segregating Mls loci and that Mls of C3H was in fact a composite of three independently segregating loci. Recently, Mlsd of CBA/J was shown to be composed of Mlsa of AKR and a product on C3H, which was presumed to be Mlsc. Based on strain distributions, this product cannot be encoded by the Mlsc originally defined by Festenstein. In the present report, three Mls specificities of CBA/H (Mlsb) are defined. Based on the strain distribution, we postulate that these specificities are controlled by three loci, three alleles/locus, or by some combination of the preceding two possibilities.
费斯滕斯坦最初将Mls基因座描述为一个单一的显性常染色体基因,有四个等位基因,定位于1号染色体的第13个连锁群中。我们随后提供的证据表明,DBA/2和CBA/J的混合淋巴细胞反应(MLR)刺激产物由两个独立分离的Mls基因座控制,并且C3H的Mls实际上是三个独立分离基因座的复合体。最近,CBA/J的Mlsd被证明由AKR的Mlsa和C3H上的一个产物组成,该产物被推测为Mlsc。基于品系分布,该产物不可能由费斯滕斯坦最初定义的Mlsc编码。在本报告中,定义了CBA/H(Mlsb)的三种Mls特异性。基于品系分布,我们推测这些特异性由三个基因座、每个基因座三个等位基因或前两种可能性的某种组合控制。