Auffray C, Lillie J W, Korman A J, Boss J M, Fréchin N, Guillemot F, Cooper J, Mulligan R C, Strominger J L
Immunogenetics. 1987;26(1-2):63-73. doi: 10.1007/BF00345456.
The nucleotide sequences of the two closely related HLA-DQ alpha and HLA-DX alpha genes have been determined. Exons coding for the signal peptide, alpha 2 and transmembrane domains are 94-99% homologous, whereas the alpha 1 exon and the promoter region have diverged as much as or more than introns and the 3' untranslated region. The promoter regions of both genes contain two short sequences thought to be important for regulation of transcription by gamma-interferon. Transfection studies established that the DQ alpha and DQ beta genes encode the HLA-DQ antigen. Transcripts of varying length are produced from different alleles as the result of the use of alternate splice and polyadenylation signals at the 3' end of the DQ alpha gene. Thus typing at the DQ alpha locus can be achieved by Northern blot analysis. No transcript of DX alpha was detected in B lymphocytes. The DX alpha gene was accurately spliced when introduced into a retroviral vector, suggesting that the lack of expression of DX alpha is not due to aberrant splice signals.
已确定两个密切相关的HLA - DQα和HLA - DXα基因的核苷酸序列。编码信号肽、α2和跨膜结构域的外显子具有94 - 99%的同源性,而α1外显子和启动子区域的差异程度与内含子及3'非翻译区相同或更大。两个基因的启动子区域都包含两个短序列,被认为对γ干扰素调节转录很重要。转染研究证实,DQα和DQβ基因编码HLA - DQ抗原。由于在DQα基因3'端使用了交替剪接和聚腺苷酸化信号,不同等位基因产生了不同长度的转录本。因此,通过Northern印迹分析可以实现DQα位点的分型。在B淋巴细胞中未检测到DXα的转录本。当将DXα基因导入逆转录病毒载体时,它能被准确剪接,这表明DXα缺乏表达并非由于异常的剪接信号。