Suppr超能文献

BALB/cJ小鼠品系的MHC基因Q8/9d不能编码Qa-2、3 I类抗原。

MHC gene Q8/9d of the BALB/cJ mouse strain cannot encode a Qa-2,3 class I antigen.

作者信息

Nakayama K, Tokito S, Pannetier C, Nakauchi H, Gachelin G

机构信息

Laboratory of Molecular Regulation of Aging, Institute of Physical and Chemical Research (RIKEN), Ibaraki, Japan.

出版信息

Immunogenetics. 1991;33(4):225-34. doi: 10.1007/BF00230499.

Abstract

We have determined the nucleotide sequence of Q8/9d gene of the BALB/c strain of mice, isolated from Steinmetz's cosmid library. As for all other class I genes of the Qa region, the Q8/9d gene spans approximately 4.7 kilobases (kb) and consists of seven exons and six introns. A seven bases deletion in exon 3 results in the occurrence of an early termination codon. Thus the Q8/9d gene cannot encode a normal class I protein. Comparison of the nucleotide sequence of the Q8/9d gene with that of other class I MHC genes revealed a stronger homology to Q7 and Q8 than to K, D, L, TL, and other Q genes. However, the gene cannot originate from a mere fusion between Q8 and Q9 genes except if the ancestor to putative Q8d was markedly different from the present Q8b gene. Using polymerase chain reaction (PCR) technology, we have confirmed the presence of a Q8/9 gene, identical to that present in cosmid 46.1, in the genome of BALB/cJ (Qa-2low). Finally, it has been reported that cDNA clone 94-A, which codes for a Qa-2 antigen, could derive from a transcript of gene Q8/9d. The nucleotide sequences of gene Q8/9d and of cDNA clone 94-A are distinctly different in their 5' regions, in spite of an almost perfect matching in their 3' regions. Thus, clone 94-A cannot derive from an mRNA transcribed from the Q8/9d gene.

摘要

我们已经确定了从小鼠BALB/c品系中分离自施泰因梅茨黏粒文库的Q8/9d基因的核苷酸序列。与Qa区域的所有其他I类基因一样,Q8/9d基因跨度约为4.7千碱基(kb),由7个外显子和6个内含子组成。外显子3中的7个碱基缺失导致出现提前终止密码子。因此,Q8/9d基因不能编码正常的I类蛋白。将Q8/9d基因的核苷酸序列与其他I类MHC基因的核苷酸序列进行比较,发现其与Q7和Q8的同源性比与K、D、L、TL及其他Q基因的同源性更强。然而,该基因不可能仅仅源于Q8和Q9基因之间的融合,除非假定的Q8d的祖先与目前的Q8b基因明显不同。使用聚合酶链反应(PCR)技术,我们已经证实在BALB/cJ(Qa-2低)的基因组中存在一个与黏粒46.1中存在的Q8/9基因相同的基因。最后,据报道,编码Qa-2抗原的cDNA克隆94-A可能源自基因Q8/9d的转录本。尽管基因Q8/9d和cDNA克隆94-A的3'区域几乎完全匹配,但其5'区域的核苷酸序列明显不同。因此,克隆94-A不可能源自从Q8/9d基因转录的mRNA。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验