Kvist S, Roberts L, Dobberstein B
European Molecular Biology Laboratory, Heidelberg, FRG.
EMBO J. 1983;2(2):245-54. doi: 10.1002/j.1460-2075.1983.tb01413.x.
The gene coding for the mouse H-2Kd antigen has been isolated by using a K-locus specific cDNA probe. The complete nucleotide sequence of the gene reveals eight exons separated by seven introns. Transcriptionally important DNA sequences (CCAAT and TATA) precede the first exon. Comparison with other H-2 genes shows extensive homology in exons as well as in introns. Two cDNA clones encoding Kd antigens have been analysed and provide evidence for at least two expressed Kd genes in the DBA/2 mouse. Comparison of the Kd antigen sequence to three other H-2 antigens indicates that gene conversion mechanism(s) act on H-2 genes. Analyses of exon donor and acceptor sites of different H-2 genes and cDNAs show that alternative splicing sites are used by different genes.
通过使用K基因座特异性cDNA探针,已分离出编码小鼠H-2Kd抗原的基因。该基因的完整核苷酸序列显示有八个外显子,被七个内含子隔开。转录重要的DNA序列(CCAAT和TATA)位于第一个外显子之前。与其他H-2基因比较表明,外显子和内含子中都存在广泛的同源性。已分析了两个编码Kd抗原的cDNA克隆,并为DBA/2小鼠中至少两个表达的Kd基因提供了证据。将Kd抗原序列与其他三种H-2抗原进行比较表明,基因转换机制作用于H-2基因。对不同H-2基因和cDNA的外显子供体和受体位点的分析表明,不同基因使用了可变剪接位点。