Dreher K L, Asundi V, Wolf B, Bruggeman L
Weis Center for Research, Geisinger Clinic, Danville, PA 17822.
J Immunol. 1990 Jul 1;145(1):325-30.
Previous studies employing Southern blot analyses have detected multiple kappa-homologous sequences within EcoRI-digested DNA isolated from kappa 1b6 homozygous rabbits and kappa 1b6 L chain secreting RMH H158 cell line. These results are very unexpected because the published partial protein sequence for the kappa 1b6 C region is incompatible with an EcoRI restriction endonuclease recognition sequence at the nucleotide level for this allotype. To determine their identity, the kappa-homologous sequences were isolated from DNA extracted from a kappa 1b6 L chain secreting RMH H158 cell line by molecular cloning. Structural analyses demonstrated these sequences to contain genetic information encoding the majority of the kappa 1b6 L chain gene locus. The protein sequence deduced from the kappa 1b6 C region gene was shown to differ from the published partial kappa 1b6 C region protein sequence at five amino acid positions. One of these differences results in a glycine to serine interchange that introduces an EcoRI restriction endonuclease recognition site within the kappa 1b6 C region gene. Subsequent genomic Southern blot analyses confirmed this structural assignment. Based on these data, the EcoRI-sensitive kappa-homologous fragments present within the genomes of the RMH H158 cell line and kappa 1b6 homozygous rabbits represent the nominal kappa 1 gene and not an alternative kappa isotype or kappa pseudogene. Rabbit Ig kappa 1 allelic nucleotide sequence homology comparisons have shown the isolated kappa 1b6 J-C gene locus to display common structural features previously identified in other kappa 1 alleles.
以往采用Southern印迹分析的研究在从κ1b6纯合兔和分泌κ1b6轻链的RMH H158细胞系中分离出的经EcoRI酶切的DNA内检测到多个κ同源序列。这些结果非常出乎意料,因为已发表的κ1b6 C区部分蛋白质序列在核苷酸水平上与该同种异型的EcoRI限制性内切酶识别序列不兼容。为了确定它们的身份,通过分子克隆从分泌κ1b6轻链的RMH H158细胞系提取的DNA中分离出κ同源序列。结构分析表明这些序列包含编码κ1b6轻链基因座大部分的遗传信息。从κ1b6 C区基因推导的蛋白质序列显示在五个氨基酸位置上与已发表的κ1b6 C区部分蛋白质序列不同。其中一个差异导致甘氨酸与丝氨酸互换,在κ1b6 C区基因内引入了一个EcoRI限制性内切酶识别位点。随后的基因组Southern印迹分析证实了这一结构定位。基于这些数据,RMH H158细胞系和κ1b6纯合兔基因组中存在的对EcoRI敏感的κ同源片段代表标称的κ1基因,而不是替代的κ同种型或κ假基因。兔Ig κ1等位基因核苷酸序列同源性比较表明,分离出的κ1b6 J-C基因座显示出先前在其他κ1等位基因中鉴定出的共同结构特征。