Carroll W L, Starnes C O, Levy R, Levy S
Department of Medicine, Stanford University School of Medicine, California 94305.
J Exp Med. 1988 Nov 1;168(5):1607-20. doi: 10.1084/jem.168.5.1607.
Idiotype variants of 38C13, a murine B cell lymphoma, have been isolated by immunoselection with antiidiotype mAbs. The V region genes for the kappa light chains and mu heavy chains expressed by these tumor cells were sequenced and compared. There was no evidence for V region somatic point mutation in this tumor. However, while the heavy chain genes were all identical, the light chain genes were all different. The light chain genes of each variant were derived from the V kappa-Ox1 gene family and joined to J kappa 4, whereas the light chain gene of the parental tumor was derived from the V kappa 9 family and joined to J kappa 2. Two of the variants used the identical V kappa gene but differed by the inclusion of a variable number of additional nucleotides in the V/J joint. Thus, the idiotypic heterogeneity of this B cell lymphoma arises as a consequence of alternative light chain rearrangements rather than point mutation. This process repetitively uses members of the same V kappa gene family. Two of the variants use the identical V kappa and J kappa gene segments but differ by the presence of extra nucleotides at the V kappa/J kappa joint.
通过用抗独特型单克隆抗体进行免疫选择,已分离出鼠源B细胞淋巴瘤38C13的独特型变体。对这些肿瘤细胞表达的κ轻链和μ重链的V区基因进行了测序和比较。在该肿瘤中没有V区体细胞点突变的证据。然而,虽然重链基因都相同,但轻链基因却各不相同。每个变体的轻链基因均源自Vκ-Ox1基因家族并与Jκ4连接,而亲代肿瘤的轻链基因则源自Vκ9家族并与Jκ2连接。其中两个变体使用相同的Vκ基因,但在V/J连接处包含数量可变的额外核苷酸,因而有所不同。因此,这种B细胞淋巴瘤的独特型异质性是由替代性轻链重排而非点突变导致的。这一过程反复使用同一Vκ基因家族的成员。其中两个变体使用相同的Vκ和Jκ基因片段,但在Vκ/Jκ连接处因存在额外核苷酸而有所不同。