Strathearn M D, Strathearn G E, Akopiantz P, Liu A Y, Paddock G V, Salser W
Nucleic Acids Res. 1978 Sep;5(9):3101-11. doi: 10.1093/nar/5.9.3101.
Nucleotide sequence analysis and restriction endonuclease mapping have been used to characterize a cDNA copy of immunoglobulin MOPC 21 Kappa mRNA clones in the bacterial plasmid pMB9. Three regions of the inserted cDNA of plasmid pL21-1 have been sequenced and match the known protein sequence at amino acid residues 1-24, 128-138 and 171-179. With these sequences to provide absolute correlations between the restriction map and the structural gene sequence it has been possible to exactly deduce the positions of all 11 of the insert restriction sites mapped within the structural gene. The pL21-1 insert contains the complete variable and constant regions as well as parts of the 3' untranslated and polypeptide leader coding sequences.
核苷酸序列分析和限制性内切酶图谱分析已用于鉴定细菌质粒pMB9中免疫球蛋白MOPC 21 κ mRNA克隆的cDNA拷贝。质粒pL21-1插入的cDNA的三个区域已测序,并与已知蛋白质序列在氨基酸残基1-24、128-138和171-179处匹配。利用这些序列在限制性图谱和结构基因序列之间提供绝对相关性,已能够精确推断出结构基因内定位的所有11个插入限制性位点的位置。pL21-1插入片段包含完整的可变区和恒定区以及3'非翻译区和多肽前导编码序列的部分。