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Translocation events in the evolution of aminoacyl-tRNA synthetases.

机译:氨酰基-tRNA合成酶进化过程中的易位事件。

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摘要

We have characterized hisS, the gene encoding the histidyl-tRNA synthetase (HisRS) from the tetraodontoid fish Fugu rubripes. The hisS gene is about 3.5 kbp long and contains 13 exons and 12 introns of 172 bp, on average. The Fugu hisS gene encodes a putative protein of 519 amino acids with the three motifs identified as signatures of class 2 aminoacyl-tRNA synthetases. A model for the shifting of intron 8 between Fugu and hamster is proposed based on the successive appearance of a cryptic splicing site followed by an insertion mutation that created a new acceptor site. In addition, sequence comparisons suggest that the hisS gene has undergone a translocation through the first intron. As a result, the Fugu HisRS has an N-terminal sequence markedly different from that in the human and hamster enzymes. We propose that similar events have been responsible for variations at the N-terminal end of other aminoacyl-tRNA synthetases. Our analysis suggests that this involves exchanges through introns of two exons encoding an ancestral 32-amino acid motif.
机译:我们已经表征了hisS,该基因编码来自四齿类鱼类河豚鱼的组氨酸-tRNA合成酶(HisRS)。 hisS基因长约3.5 kbp,平均包含13个外显子和12个172 bp的内含子。 Fugu hisS基因编码一个519个氨基酸的推定蛋白质,具有被识别为2类氨酰基tRNA合成酶特征的三个基序。基于隐性剪接位点的连续出现,然后是产生新受体位点的插入突变,提出了内含子8在Fugu和仓鼠之间移动的模型。另外,序列比较表明hisS基因已经通过第一内含子发生了易位。结果,河豚属HisRS的N端序列与人和仓鼠酶中的N端序列明显不同。我们建议类似的事件已负责其他氨酰基-tRNA合成酶的N末端的变化。我们的分析表明,这涉及通过编码一个祖先的32个氨基酸基序的两个外显子的内含子进行交换。

著录项

  • 作者

    Brenner, S; Corrochano, L M;

  • 作者单位
  • 年度 1996
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  • 原文格式 PDF
  • 正文语种 en
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