Das H K, Biro P A, Cohen S N, Erlich H A, von Gabain A, Lawrance S K, Lemaux P G, McDevitt H O, Peterlin B M, Schulz M F, Sood A K, Weissman S M
Proc Natl Acad Sci U S A. 1983 Mar;80(6):1531-5. doi: 10.1073/pnas.80.6.1531.
We have synthesized 175-nucleotide-long probes for the DNA of human histocompatibility antigens HLA-DR alpha and beta by extending on poly(A)+ mRNA from B-cell lines with short synthetic deoxyribonucleotide primers complementary to the predicted nucleotide sequence of the NH2 terminus of both polypeptides. The synthesis of the probe for the alpha-chain DNA was a two-step process starting with 11-mers which were extended by dideoxynucleotide chain termination experiments to a 20-mer of predicted sequence. The synthesized 20-mer was then used to generate a 175-nucleotide cDNA probe which was shown to encode the appropriate amino acids for the alpha chain and was used to select a human genomic DNA clone containing the coding sequences for HLA-DR alpha. For the beta polypeptide an 18-mer homologous to the NH2-terminal sequence of a cDNA clone from another B-cell line was used to extend on poly(A)+ mRNA isolated from a B-cell line. Preliminary sequence analysis of a 175-base-long extension product indicates a match of the cDNA sequence to the published sequence of a clone for HLA-DR beta. Information from these extension experiments helps to establish the sensitivity and specificity of the primer extension method.
我们通过用与两种多肽NH2末端预测核苷酸序列互补的短合成脱氧核糖核苷酸引物,在B细胞系的聚腺苷酸加尾mRNA上进行延伸,合成了针对人类组织相容性抗原HLA - DRα和β DNA的175个核苷酸长的探针。α链DNA探针的合成是一个两步过程,从11聚体开始,通过双脱氧核苷酸链终止实验将其延伸至预测序列的20聚体。然后,合成的20聚体用于生成一个175个核苷酸的cDNA探针,该探针被证明可编码α链的相应氨基酸,并用于筛选包含HLA - DRα编码序列的人类基因组DNA克隆。对于β多肽,使用与另一个B细胞系cDNA克隆的NH2末端序列同源的18聚体,在从一个B细胞系分离的聚腺苷酸加尾mRNA上进行延伸。对一个175个碱基长的延伸产物的初步序列分析表明,该cDNA序列与已发表的HLA - DRβ克隆序列匹配。这些延伸实验的信息有助于确定引物延伸方法的灵敏度和特异性。