McKean D, Huppi K, Bell M, Staudt L, Gerhard W, Weigert M
Proc Natl Acad Sci U S A. 1984 May;81(10):3180-4. doi: 10.1073/pnas.81.10.3180.
We have examined the amino-terminal sequence of the kappa light chains of a set of monoclonal antibodies specific for one of the major antigenic determinants (Sb) on the influenza virus PR8[A/PR/8/34(H1N1)] hemagglutinin molecule. This set was believed to be structurally related from earlier serological analysis that typed these kappa chains as members of the variable (V) region V kappa 21 group [ Staudt , L. M. & Gerhard , W. (1983) J. Exp. Med. 157, 678-704]. Our sequence analysis confirms and extends this conclusion; all examples of this set belong to a subgroup of the V kappa 21 group, V kappa 21C . A special feature of this set of kappa light chains is that all examples were derived from the same mouse (designated H36 ). This sequence analysis along with the characterization of gene rearrangements at the kappa light chain loci of these hybridomas is consistent with the idea that certain members of this set are the progeny of one or two lymphocytes. Because of this potential clonal relationship, we can reach several conclusions about the diversity observed among these kappa light chains: (i) the diversity is due to somatic mutation, (ii) somatic mutations occur sequentially and accumulate in the first complementarity-determining region, and (iii) the extent of somatic variation in this sample is high, suggesting a somatic mutation rate of about 10(-3) per base pair per generation.
我们检测了一组针对流感病毒PR8[A/PR/8/34(H1N1)]血凝素分子上一种主要抗原决定簇(Sb)的单克隆抗体κ轻链的氨基末端序列。根据早期血清学分析,这组抗体被认为在结构上具有相关性,这些κ链被归类为可变(V)区Vκ21组的成员[施陶特,L.M. & 格哈德,W.(1983年)《实验医学杂志》157, 678 - 704]。我们的序列分析证实并扩展了这一结论;这组抗体的所有实例都属于Vκ21组的一个亚组,即Vκ21C。这组κ轻链的一个特殊之处在于,所有实例都来自同一只小鼠(命名为H36)。该序列分析以及这些杂交瘤κ轻链基因座处基因重排的特征,与这组抗体中的某些成员是一两个淋巴细胞后代的观点一致。由于这种潜在的克隆关系,我们可以就这些κ轻链中观察到的多样性得出几个结论:(i)多样性是由于体细胞突变,(ii)体细胞突变依次发生并在第一个互补决定区积累,(iii)该样本中体细胞变异的程度很高,表明每代每碱基对的体细胞突变率约为10^(-3)。