Clarke C, Berenson J, Goverman J, Boyer P D, Crews S, Siu G, Calame K
Nucleic Acids Res. 1982 Dec 11;10(23):7731-49. doi: 10.1093/nar/10.23.7731.
The V1 gene encodes the heavy chain variable region of antibodies that bind to phosphorylcholine in the Balb/c mouse. V1 genes have been cloned from mouse sperm DNA, an IgM-producing tumor HPCM2 and an IgA-producing tumor M167. The transcription start site of the V1 gene has been mapped 63 +/- 1 base pairs from the coding sequence for both alpha and mu transcripts. Comparison of flanking DNA sequence 574 base pairs 5' to the V1 transcription start site in sperm, HPCM2 and M167 DNA reveals that sperm and HPCM2 sequences are completely identical in this region and the M167 sequence differs from them by a single base change. Although the coding region of the V1 gene has undergone a high (4%) rate of somatic mutation in M167 we demonstrate that the somatic mutation mechanism stops near the transcription start site. These results demonstrate that initiation of V1 gene transcription remains unchanged with respect to location and 5' sequences throughout B-cell development.
V1基因编码与Balb/c小鼠中的磷酸胆碱结合的抗体重链可变区。V1基因已从小鼠精子DNA、产生IgM的肿瘤HPCM2和产生IgA的肿瘤M167中克隆出来。V1基因的转录起始位点已被定位在距α和μ转录本编码序列63±1个碱基对处。对精子、HPCM2和M167 DNA中V1转录起始位点5'端574个碱基对的侧翼DNA序列进行比较,结果显示精子和HPCM2序列在该区域完全相同,而M167序列与它们仅存在一个碱基的差异。尽管V1基因的编码区在M167中经历了较高(4%)的体细胞突变率,但我们证明体细胞突变机制在转录起始位点附近停止。这些结果表明,在整个B细胞发育过程中,V1基因转录的起始在位置和5'序列方面保持不变。