Sasso E H, Willems van Dijk K, Bull A, van der Maarel S M, Milner E C
Virginia Mason Research Center, Seattle, WA 98101.
J Immunol. 1992 Aug 15;149(4):1230-6.
In a study of human VH gene heterogeneity, we have previously used sequence-specific oligonucleotide probes to demonstrate polymorphism of 56pl and three highly homologous VH3 germline elements. We now extend these findings with VH nucleotide sequences obtained from a person who possesses restriction fragments corresponding to each of these four VH3 genes. From a lambda-phage library of genomic DNA, distinct phage clones containing putative 56pl, hv3005, 1.9III, and hv3019b9 genes were selected by screening with oligonucleotide probes. PCR amplification, subcloning, and sequencing from the respective clones 3d216, 3d24, 3d28, and 3d277, yielded exact 56p1, hv3005, 1.9III, and hv3019b9 nucleotide sequences. A panel of oligonucleotide probes was shown to hybridize to these cloned VH3 genes with exact specificity, demonstrating the ability of the probes to predict the sequence of detected target DNA. Based on their chromosomal organization and their previously determined distribution in the population, these VH3 genes represent at least three distinct loci. From each of the VH3-containing phage clones, a VH4 element was also identified and sequenced. Linked to 3d24 and 3d28, respectively, were VH4 sequences identical to hv4005 and 1.9II, corroborating previous reports. The VH4 elements linked to 3d216 and 3d277 were distinct from published VH4 sequences. Nucleotide sequence homology was 97 to 99% among the VH3 sequences, and 93 to 99% among the VH4. These findings indicate that the VH3-VH4 gene pairs we have identified are a repeated germline motif, apparently resulting from multiple duplications of tandemly arrayed VH genes.
在一项关于人类VH基因异质性的研究中,我们之前使用序列特异性寡核苷酸探针来证明56pl以及三个高度同源的VH3种系元件的多态性。现在,我们利用从一个拥有与这四个VH3基因各自对应的限制性片段的人身上获得的VH核苷酸序列,扩展了这些发现。通过用寡核苷酸探针筛选,从基因组DNA的λ噬菌体文库中选择了包含推定的56pl、hv3005、1.9III和hv3019b9基因的不同噬菌体克隆。从各自的克隆3d216、3d24、3d28和3d277进行PCR扩增、亚克隆和测序,得到了精确的56p1、hv3005、1.9III和hv3019b9核苷酸序列。一组寡核苷酸探针被证明能以精确的特异性与这些克隆的VH3基因杂交,证明了探针预测检测到的靶DNA序列的能力。基于它们的染色体组织及其先前确定的群体分布,这些VH3基因代表至少三个不同的基因座。从每个含VH3的噬菌体克隆中,还鉴定并测序了一个VH4元件。分别与3d24和3d28相连的是与hv4005和1.9II相同的VH4序列,证实了先前的报道。与3d216和3d277相连的VH4元件与已发表的VH4序列不同。VH3序列之间的核苷酸序列同源性为97%至99%,VH4之间为93%至99%。这些发现表明,我们鉴定出的VH3 - VH4基因对是一个重复的种系基序,显然是由串联排列的VH基因多次重复产生的。