Auffray C, Nageotte R, Sikorav J L, Heidmann O, Rougeon F
Gene. 1981 May;13(4):365-74. doi: 10.1016/0378-1119(81)90016-0.
The cDNAs complementary to mouse immunoglobulin alpha heavy chain mRNAs have been cloned into the PstI site of the plasmid vector pBR322. Recombinant plasmids have been identified by hybrid-arrested translation and purification of alpha heavy chain mRNA on DNA-DBM filters. The nucleotide sequence of the inserts encodes the constant and 3' untranslated regions of the alpha heavy chain mRNA. The CH3 domains of human and mouse alpha chains are highly homologous, including a 36 amino acid fragment not reported in the protein sequence (Robinson and Appella, 1980). As in the case of the mu secreted heavy chain, the alpha heavy chain contains a carboxy terminal piece of 20 amino acids.
与小鼠免疫球蛋白α重链mRNA互补的cDNA已被克隆到质粒载体pBR322的PstI位点。通过杂交捕获翻译以及在DNA-偶氮苯甲酰甲基纤维素滤膜上纯化α重链mRNA来鉴定重组质粒。插入片段的核苷酸序列编码α重链mRNA的恒定区和3'非翻译区。人和小鼠α链的CH3结构域高度同源,包括蛋白质序列中未报道的一个36个氨基酸的片段(罗宾逊和阿佩拉,1980年)。与μ分泌型重链的情况一样,α重链含有一个20个氨基酸的羧基末端片段。