Max E E, Seidman J G, Leder P
Proc Natl Acad Sci U S A. 1979 Jul;76(7):3450-4. doi: 10.1073/pnas.76.7.3450.
Immunoglobulin kappa chain gene formation involves site-specific somatic recombination between one of several hundred germ-line variable region genes and a joining site (or "J segment") encoded close to the constant region gene. We have cloned and determined the nucleotide sequence of major portions of the recombination region of the mouse kappa gene and discovered a series of five such J segments spread out along a segment of DNA 2.4 kilobases from the kappa constant region gene. These J segments encode the 13 COOH-terminal amino acids of the variable region, probably including amino acids involved in the antigen combining site and in heavy/light chain contacts. The J segments also display striking sequence homology to one another in both their coding and immediately flanking sequences. Major elements of a short palindrome--CAC(TA)GTG--are preserved adjacent to the recombination sites of both variable and J region genes and constitute inverted repeats at both ends of the sequences to be joined. These palindromes can be written as a hypothetical stem structure that draws variable and J regions together, providing a possible molecular basis for the DNA joining event. Four of the J segments that we have discovered encode amino acid sequences already found in myeloma proteins. By altering the frame of recombination, we can account for additional light chain amino acid sequences, suggesting that the V/J joining event might generate antibody diversity somatically both by using different combinations of variable and J region genes and by using alternative joining frames.
免疫球蛋白κ链基因的形成涉及数百个种系可变区基因之一与靠近恒定区基因编码的连接位点(或“J片段”)之间的位点特异性体细胞重组。我们已经克隆并确定了小鼠κ基因重组区主要部分的核苷酸序列,并发现了一系列五个这样的J片段,它们沿着距κ恒定区基因2.4千碱基的一段DNA分布。这些J片段编码可变区的13个羧基末端氨基酸,可能包括参与抗原结合位点和重链/轻链接触的氨基酸。J片段在其编码序列和紧邻的侧翼序列中也显示出彼此显著的序列同源性。短回文序列——CAC(TA)GTG——的主要元件在可变区和J区基因的重组位点附近得以保留,并在待连接序列的两端构成反向重复序列。这些回文序列可以写成一种假设的茎结构形式,将可变区和J区拉到一起,为DNA连接事件提供了一种可能的分子基础。我们发现的四个J片段编码的氨基酸序列已在骨髓瘤蛋白中发现。通过改变重组框架,我们可以解释其他轻链氨基酸序列,这表明V/J连接事件可能通过使用可变区和J区基因的不同组合以及通过使用替代连接框架在体细胞中产生抗体多样性。