Reilly E B, Reilly R M, Breyer R M, Sauer R T, Eisen H N
J Immunol. 1984 Jul;133(1):471-5.
To learn about the V lambda gene segments that are expressed in lambda 3 light chains, the most recently identified lambda-chain subtype in inbred mice, we determined partial amino acid sequences of the V regions of two of these chains, L5-8 and Lc49 . The partial sequences were extended by establishing the complete V region sequence of cDNA for the lambda-chain mRNA from the hybridoma (RZ 5-8) and the myeloma ( CBPC -49) that produce these chains. The primer extension method used to sequence the cDNA is described in detail, because the same primer (a synthetic heptadecadeoxynucleotide ) can be used for sequencing cDNA for lambda-chains of all three subtypes of inbred mice and probably for lambda-chains from some other vertebrate species as well. The results confirm earlier preliminary findings that for both chains the V region is encoded by the V lambda 1 and J lambda 3 gene segments. The unmutated germ-line sequences of these gene segments are present in both chains, but the two chains, nevertheless, differ at codon 97, the V lambda-J lambda boundary. A T/G difference in the third position of this codon resulted in a codon for histidine (CAT) in one chain (L5-8) and for glutamine (CAG) in the other chain ( Lc49 ). This difference can be accounted for by variation in the site of V lambda 1-J lambda 3 recombination. Though the V region amino acid sequences of L5-8 and Lc49 differ only by the His/Gln substitution at position 97, the two chains have been shown (manuscript in preparation) to differ in their ability to form an effective combining site for the 2,4-dinitrophenyl group.
为了解在λ3轻链(近交系小鼠中最近鉴定出的λ链亚型)中表达的Vλ基因片段,我们测定了其中两条链L5-8和Lc49的V区部分氨基酸序列。通过确定产生这些链的杂交瘤(RZ 5-8)和骨髓瘤(CBPC -49)的λ链mRNA的cDNA完整V区序列,扩展了部分序列。详细描述了用于cDNA测序的引物延伸方法,因为相同的引物(一种合成的十七脱氧核苷酸)可用于对近交系小鼠所有三种亚型的λ链cDNA进行测序,可能也可用于其他一些脊椎动物物种的λ链测序。结果证实了早期的初步发现,即对于这两条链,V区均由Vλ1和Jλ3基因片段编码。这些基因片段的未突变种系序列存在于两条链中,但两条链在密码子97(Vλ-Jλ边界)处仍存在差异。该密码子第三位的T/G差异导致一条链(L5-8)中的组氨酸密码子(CAT)和另一条链(Lc49)中的谷氨酰胺密码子(CAG)。这种差异可归因于Vλ1-Jλ3重组位点的变异。尽管L5-8和Lc49的V区氨基酸序列仅在第97位的His/Gln替换上有所不同,但已表明(正在准备的手稿)这两条链在形成针对2,4-二硝基苯基基团的有效结合位点的能力上存在差异。