Weigert M, Perry R, Kelley D, Hunkapiller T, Schilling J, Hood L
Nature. 1980 Jan 31;283(5746):497-9. doi: 10.1038/283497a0.
The variable regions of mouse kappa (kappa) chains are coded for by multiple variable (V) gene segments and multiple joining (J) gene segments. The V kappa gene segments code for residues 1 to 95; the J kappa gene segments code for residues 96 to 108 (refs 1-3). This gene organisation is similar to that encoding the V lambda regions. Diversity in V kappa regions arises from several sources: (1) there are multiple germ-line V kappa gene segments and J kappa gene segments; (2) combinatorial joining of V kappa gene segments with different germline J kappa gene segments; and possibly, (3) somatic point mutation, as postulated for V lambda gene segments. Also, from a comparison of the number of germ-line J kappa gene segments and amino acid sequences, it has been suggested that J kappa region sequences may be determined by the way V kappa and J kappa gene segments are joined. This report supports this model by directly associating various J kappa sequences with given J kappa gene segments.
小鼠κ链的可变区由多个可变(V)基因片段和多个连接(J)基因片段编码。Vκ基因片段编码第1至95位氨基酸残基;Jκ基因片段编码第96至108位氨基酸残基(参考文献1 - 3)。这种基因组织与编码Vλ区的基因组织相似。Vκ区的多样性源于多个方面:(1)存在多个种系Vκ基因片段和Jκ基因片段;(2)Vκ基因片段与不同种系Jκ基因片段的组合连接;并且可能(3)体细胞点突变,这与Vλ基因片段的推测情况相同。此外,通过对种系Jκ基因片段数量和氨基酸序列的比较,有人提出Jκ区序列可能由Vκ和Jκ基因片段的连接方式决定。本报告通过将各种Jκ序列与特定的Jκ基因片段直接关联,支持了这一模型。