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首页> 外文期刊>The Journal of Experomental Medicine >Molecular evidence that the H-2D and H-2L genes arose by duplication. Differences between the evolution of the class I genes in mice and humans.
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Molecular evidence that the H-2D and H-2L genes arose by duplication. Differences between the evolution of the class I genes in mice and humans.

机译:H-2D和H-2L基因通过重复产生的分子证据。小鼠和人类中I类基因的进化之间的差异。

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To resolve issues regarding the evolution of D region class I MHC genes and their relationship to other class I-encoding regions of the mouse, as well as man, we characterized the class I genes from the Dq region of the B10.AKM mouse strain. The Dq region was selected because it was known to express multiple gene products, yet two of the products previously characterized have structural features in common with the Ld molecule. Since DNA hybridization data defined similarities between the Dd and Dq regions, we used low-copy genomic or oligonucleotide probes derived from the Dd region of BALB/c (H-2d) to screen a B10.AKM cosmid library. Cosmid clones containing Dq, D2q, D3q, D4q, Lq, and Q1q genes have been isolated and aligned with the corresponding genes of the BALB/c MHC, thus demonstrating a similar gene organization. The two classical transplantation genes, Dq and Lq were found to be strikingly similar to each other such that exons 1-3 of Dq and Lq, are approximately 97% homologous, and exons 4-8 are identical. Furthermore, the implied amino acid sequences of both Lq and Dq molecules show considerable homology to Ld, particularly in regions presumed to be involved in ligand binding. These comparisons suggest not only that the Dq and Lq genes arose from the duplication of an Ld-like progenitor, but also that there is a selective advantage for the maintenance of an Ld-like structure. In addition, the 5' portion of the D4q gene was sequenced and found to have a 13-bp deletion and a 4-bp insertion within the alpha 2 exon. These result in a frame shift that creates a premature termination codon and potential polyadenylation site, respectively. Thus, D4q does not encode a typical class I molecule. Sequence comparisons suggest that the D4q gene did not arise from a duplication event involving an Ld-like gene such as Dq and Lq. Interestingly, the D4q molecule, if produced, would have amino acid residues in common with K and/or Q molecules that differ from those observed in D/L molecules. These findings, in conjunction with hybridization data, provide evidence that the D2, D3, and D4 genes were derived from Q genes by an unequal crossover event. Additional hybridization data using low-copy D region probes suggest that several different D region gene organizations exist among mice of different haplotypes. These and other recent molecular studies provide multiple examples of expansion and contraction of the class I genes in the D region.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:若要解决有关D区I类MHC基因的进化以及它们与小鼠以及人类其他I类编码区之间关系的问题,我们从B10.AKM小鼠品系的Dq区表征了I类基因。选择Dq区域是因为已知它可以表达多种基因产物,但先前表征的两种产物具有与Ld分子相同的结构特征。由于DNA杂交数据定义了Dd和Dq区之间的相似性,因此我们使用衍生自BALB / c(H-2d)Dd区的低拷贝基因组或寡核苷酸探针筛选B10.AKM粘粒文库。含有Dq,D2q,D3q,D4q,Lq和Q1q基因的粘粒克隆已被分离出来,并与BALB / c MHC的相应基因进行比对,从而证明了类似的基因组织。发现两个经典的移植基因Dq和Lq非常惊人地相似,因此Dq和Lq的外显子1-3具有大约97%的同源性,外显子4-8是相同的。此外,Lq和Dq分子的隐含氨基酸序列与Ld表现出相当的同源性,特别是在推测参与配体结合的区域。这些比较不仅表明Dq和Lq基因是由Ld样祖细胞的复制产生的,而且还具有维持Ld样结构的选择性优势。另外,对D4q基因的5'部分进行了测序,发现在α2外显子内具有13bp的缺失和4bp的插入。这些导致移码,分别产生过早的终止密码子和潜在的聚腺苷酸化位点。因此,D4q不编码典型的I类分子。序列比较表明,D4q基因不是由涉及Ld样基因(例如Dq和Lq)的复制事件引起的。有趣的是,如果产生D4q分子,则其K和/或Q分子将具有与D / L分子中观察到的氨基酸残基相同的氨基酸残基。这些发现与杂交数据一起提供了证据,表明D2,D3和D4基因是通过不相等的交叉事件从Q基因衍生而来的。使用低拷贝D区探针的其他杂交数据表明,在不同单倍型小鼠之间存在几种不同的D区基因组织。这些以及其他近期的分子研究提供了D类I类基因扩增和收缩的多个例子。(摘要截短为400字)

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