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Mutational hot spots in Ig V region genes of human follicular lymphomas

机译:人滤泡性淋巴瘤Ig V区基因的突变热点

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摘要

The genes coding for the Ig light chains expressed in two cases of human follicular lymphoma were cloned and sequenced. In each case, multiple independent isolates of the tumor population were compared. Although each tumor represented a single clone of B cells with a unique V/J joint, different cells within each tumor had accumulated multiple point mutations in the V gene during clonal expansion. Most of the mutations observed were silent, but some resulted in amino acid replacements. Identical silent mutations were often observed in independent isolates of each tumor. By combining the current data with VH sequences obtained previously from the same cells, it was apparent that the repetitive silent mutations could not be explained solely by a genealogic tree. Such mutations could represent hot spots whose tendency to mutate may be influenced by neighboring DNA sequences or by the methylation of specific cytosine residues.
机译:克隆并测序了在两例人滤泡性淋巴瘤中表达的编码Ig轻链的基因。在每种情况下,都比较了肿瘤群体的多个独立分离株。尽管每个肿瘤代表具有唯一V / J接头的B细胞的单个克隆,但每个肿瘤内的不同细胞在克隆扩增过程中在V基因中积累了多个点突变。观察到的大多数突变都是沉默的,但有些导致氨基酸置换。在每个肿瘤的独立分离物中经常观察到相同的沉默突变。通过将当前数据与先前从相同细胞中获得的VH序列相结合,很明显,重复的沉默突变不能仅通过家谱树来解释。此类突变可能代表热点,其突变趋势可能受到邻近DNA序列或特定胞嘧啶残基甲基化的影响。

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