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日本河豚红鳍东方鲀缬氨酰-tRNA合成酶基因的基因组结构与序列分析

Genomic structure and sequence analysis of the valyl-tRNA synthetase gene of the Japanese pufferfish, Fugu rubripes.

作者信息

Lim E H, Corrochano L M, Elgar G, Brenner S

机构信息

Department of Medicine, Addenbrookes Hospital, Cambridge, United Kingdom.

出版信息

DNA Seq. 1997;7(3-4):141-51. doi: 10.3109/10425179709034030.

Abstract

The genomic sequence and exon-intron organisation of the valyl-tRNA synthetase gene in the Japanese pufferfish, Fugu rubripes, have been determined. This single-copy Fugu gene spans 8.5 kb, about 2.5 times smaller than that in man (21 kb). It contains 29 exons, with the largest intron being 1008 bp. The predicted polypeptide consists of 1217 amino acids, with a molecular weight of 138 kD and an isoelectric point of 7.27. It shares 40% identity in the overlapping region with its homolog in bacteria, 47% with yeast, and 67% with man. The Fugu gene has an additional N-terminal sequence which shows strong similarity to elongation factory-1gamma, a feature it shares only with the human sequence, but not with any other lower eukaryote or prokaryote studied so far. This N-terminal segment is encoded in the first six exons, suggesting their capture by a translocation through introns. Indeed, the acquisition of extra domains to perform related functions in RNA splicing and translation of polypeptides has already been observed in other aminoacyl-tRNA synthetases. Two cDNA sequences of human valyl-tRNA synthetase have been published, with discrepancies between them. Aided by comparisons with the Fugu gene, three of these discrepancies have been resolved, involving the elucidation of the sequence and positions of two introns. This compact vertebrate genome has demonstrated its value as a tool for the analysis of genes at the genomic level.

摘要

已确定日本河豚红鳍东方鲀缬氨酰 - tRNA合成酶基因的基因组序列和外显子 - 内含子组织。这个单拷贝的河豚基因跨度为8.5 kb,大约是人相应基因(21 kb)的2.5倍小。它包含29个外显子,最大的内含子为1008 bp。预测的多肽由1217个氨基酸组成,分子量为138 kD,等电点为7.27。它在重叠区域与细菌中的同源物有40%的同一性,与酵母有47%的同一性,与人类有67%的同一性。河豚基因有一个额外的N端序列,与延伸因子1γ显示出很强的相似性,这是它仅与人类序列共有的特征,而与迄今为止研究的任何其他低等真核生物或原核生物都没有。这个N端片段在前六个外显子中编码,表明它们是通过内含子易位捕获的。实际上,在其他氨酰 - tRNA合成酶中已经观察到获得额外结构域以在RNA剪接和多肽翻译中执行相关功能。已发表了两个人类缬氨酰 - tRNA合成酶的cDNA序列,但它们之间存在差异。借助与河豚基因的比较,其中三个差异已得到解决,涉及阐明两个内含子的序列和位置。这个紧凑的脊椎动物基因组已证明其作为基因组水平基因分析工具的价值。

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