Lieber M R, Hesse J E, Mizuuchi K, Gellert M
Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
Genes Dev. 1987 Oct;1(8):751-61. doi: 10.1101/gad.1.8.751.
We have examined the level of immunoglobulin gene V(D)J recombination activity in a number of cell lines derived from lymphoid or nonlymphoid lineages. The assay we employed uses extrachromosomal DNA as substrate and thereby avoids difficulties associated with the use of chromosomally integrated substrates. The recombination activity decreases during B-lymphoid development. It is highest at the earliest stages of committed B-cell differentiation and then falls progressively, reaching undetectable levels at the mature B-cell stage. The activity is also present in multipotential progenitors of myeloid cells and in pre-T cells but not mature T cells. No activity was found in several nonhematopoietic cell lines. Recombination was seen only among substrate molecules which had replicated in the eukaryotic cells. Several possible interpretations of this result are discussed.
我们检测了多种源自淋巴系或非淋巴系谱系的细胞系中免疫球蛋白基因V(D)J重组活性的水平。我们采用的检测方法使用染色体外DNA作为底物,从而避免了使用染色体整合底物所带来的困难。在B淋巴细胞发育过程中,重组活性降低。它在定向B细胞分化的最早阶段最高,然后逐渐下降,在成熟B细胞阶段达到无法检测的水平。该活性也存在于髓系细胞的多能祖细胞和前T细胞中,但不存在于成熟T细胞中。在几种非造血细胞系中未发现活性。重组仅在真核细胞中复制的底物分子之间出现。讨论了该结果的几种可能解释。