Korsmeyer S J, Hieter P A, Ravetch J V, Poplack D G, Waldmann T A, Leder P
Proc Natl Acad Sci U S A. 1981 Nov;78(11):7096-100. doi: 10.1073/pnas.78.11.7096.
We have used a special class of human acute lymphocytic leukemias, the common "non-T/non-B" cell type, to define a hierarchy of genetic rearrangements that occur during the earliest stages of B-cell maturation. This has allowed us to identify intermediate cells predicted by a hierarchial model in which immunoglobulin heavy chain variable region gene formation precedes that of light chain and in which kappa light chain gene formation precedes that of lambda. The model emphasizes the flexible nature of immunoglobulin gene recombination that not infrequently produces aberrant or null genes that are phenotypically excluded from expression. Remaining alleles or isotypic genes can then be utilized as "spares" undergoing recombination until a valid gene is formed. Significantly, the excluded allele or isotype is frequently deleted from the genome. In addition to defining a pathway of genetic maturation, this analysis provides a powerful means to further classify cases of non-T/non-B-cell acute lymphocytic leukemia, most of which seem to reside at early stages along the B-cell pathway of differentiation.
我们利用了一类特殊的人类急性淋巴细胞白血病,即常见的“非T/非B”细胞类型,来定义在B细胞成熟最早阶段发生的基因重排层次结构。这使我们能够识别出由层次模型预测的中间细胞,在该模型中,免疫球蛋白重链可变区基因的形成先于轻链,且κ轻链基因的形成先于λ轻链。该模型强调了免疫球蛋白基因重组的灵活性,这种重组经常产生异常或无效基因,这些基因在表型上被排除表达。剩余的等位基因或同型基因随后可作为“备用”进行重组,直到形成有效基因。值得注意的是,被排除的等位基因或同型基因经常从基因组中删除。除了定义基因成熟途径外,该分析还提供了一种强大的手段,可进一步对非T/非B细胞急性淋巴细胞白血病病例进行分类,其中大多数似乎处于B细胞分化途径的早期阶段。