Devlin J J, Weiss E H, Paulson M, Flavell R A
EMBO J. 1985 Dec 1;4(12):3203-7. doi: 10.1002/j.1460-2075.1985.tb04066.x.
DNA restriction maps of the major histocompatibility complex and hybridization with low copy probes have previously revealed strong homology between the Q6-Q7 and the Q8-Q9 class I gene pairs in the Qa2 region of the C57BL/10 mouse. After DNA sequence analysis of the Q7, Q8 and Q9 genes, we have compared the Q7 gene with its apparent allele, 27.1, from the BALB/c mouse; the 99% homology between Q7 and 27.1 indicates that this is a non-polymorphic gene. Comparison of Q7 with Q9, its homologue in the Q8-Q9 gene pair, revealed greater than 99% homology, thus supporting our proposal that the Qa2 region has evolved by the duplication of gene pairs. Q7 was also found to be homologous (93%) to Q8, the second member of the Q8-Q9 pair. However, the first exon (encoding the leader sequence) as well as the first intron of Q7 and Q8, which are presumably not subject to strong selective pressure, are essentially identical in nucleotide sequence (having only one mismatch), which suggests that greater than 200 bp of DNA may have been exchanged by gene conversion. Furthermore, transcripts of both Q7 and Q8 would have termination codons derived from the exon that normally encodes the transmembrane domain, thus these genes could encode either membrane-bound class I proteins that lack a cytoplasmic protein domain or class I proteins that are secreted.
主要组织相容性复合体的DNA限制酶切图谱以及与低拷贝探针的杂交结果先前已显示,在C57BL/10小鼠的Qa2区域中,Q6-Q7和Q8-Q9这两个I类基因对之间存在很强的同源性。在对Q7、Q8和Q9基因进行DNA序列分析后,我们将Q7基因与其在BALB/c小鼠中明显的等位基因27.1进行了比较;Q7和27.1之间99%的同源性表明这是一个非多态性基因。将Q7与Q8-Q9基因对中的同源基因Q9进行比较,发现同源性大于99%,从而支持了我们关于Qa2区域是通过基因对重复进化而来的提议。还发现Q7与Q8-Q9对中的第二个成员Q8同源(93%)。然而,Q7和Q8的第一个外显子(编码前导序列)以及第一个内含子,推测它们不受强烈的选择压力,在核苷酸序列上基本相同(只有一个错配),这表明可能有超过200 bp的DNA通过基因转换进行了交换。此外,Q7和Q8的转录本都会有来自通常编码跨膜结构域的外显子的终止密码子,因此这些基因可能编码缺乏细胞质蛋白结构域的膜结合I类蛋白或分泌型I类蛋白。