首页> 外文期刊>The journal of immunology >Expression of the a, x, and y Variable Region Genes of Heavy Chains among IgG, IgM, and IgA Molecules of Normal and a Locus Allotype-Suppressed Rabbits
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Expression of the a, x, and y Variable Region Genes of Heavy Chains among IgG, IgM, and IgA Molecules of Normal and a Locus Allotype-Suppressed Rabbits

机译:IgG,IgM和IgA分子中的重链的A,X和Y可变区基因的表达和源位抑制兔的IgA分子

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The contribution of the VH subgroup genes, a, x and y, to the formation of individual IgG molecules has been studied in normal and a locus allotype-suppressed rabbits. Using anti-x32, anti-y33 and antisera to the a locus allotypes (anti-a1, anti-a2 and anti-a3), we used indirect precipitation of 125I-labeled IgG or Fab of specific allotype or inhibition of precipitation for the quantitative analyses. In normal rabbits homozygous with respect to the a locus, about 70 to 90% of the total IgG molecules possess the a locus allotypic specificities and most or all of the remaining molecules, depending on the genotype, could be accounted for as x32 or y33 molecules. Additional IgG molecules with unknown allotypic specificities for the V H region were found in two normal a3 rabbits and in an a1 allotype-suppressed rabbit; these molecules are probably the products of allelic alternatives to x32 and/or y33. Allotype-suppression of a locus molecules was compensated for by an increase in the number of molecules synthesized by closely linked V H subgroup genes, x and y . A similar ratio of the a2, x32, and y33 molecules was observed among Ig fractions with different net electrical charges. In a partially a2-suppressed rabbit, the results of indirect precipitation and sequential precipitation indicated that no two of the allotypic specificities, a2, x32, or y33, are located on the same IgG molecule or on the same Fab fragment. In homozygotes, a locus suppression was found for IgM and IgA as well as for IgG. The expression of a selected V H gene in a cell synthesizing Ig molecules results from linked gene exclusion apparently independent of C H gene selection.
机译:在正常和基因座同种型抑制兔子中已经研究了VH亚组基因,A,X和Y对形成单个IgG分子的贡献。使用抗X32,抗Y33和抗血清到轨迹同质型(抗A1,抗A2和抗A3),我们使用间接沉淀的125I标记的IgG或Fab的特异性分配或抑制沉淀的定量分析。在相对于轨迹的正常兔中,约70%至90%的总IgG分子具有基因座均等特异性,并且根据基因型,大多数或所有剩余分子可以占X32或Y33分子。在两个正常A3兔和A1单型抑制兔中发现了具有未知的v H区域的异丙型特异性的另外的IgG分子。这些分子可能是X32和/或Y33的等位基因替代品的产物。通过紧密连接的VH亚组基因,x和y合成的分子数量的增加来补偿轨迹分子的源型抑制。在具有不同净电荷的IG级分之间观察到A2,X32和Y33分子类似的比例。在局部A2抑制的兔中,间接沉淀和顺序沉淀的结果表明,没有两种等型特异性,A2,X32或Y33位于同一IgG分子上或在同一Fab片段上。在纯合蛋白中,发现IgM和IgA以及IgG的基因座抑制。在细胞中选择的VH基因在合成IG分子中的表达是由连接的基因排除的显然与C H基因选择无关。

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