cDNA Cloning of Polypeptide Chain Elongation Factor 1α from Medaka Oryzias latipes

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  • Kinoshita Masato
    Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University
  • Nakata Takahiro
    Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University Department of Anatomy, Faculty of Medicine, National Defense Medical College
  • Adachi Kousuke
    Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University
  • Yabe Taijiro
    Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University
  • Yokoyama Yoshihiro
    Interdisciplinary Research Institute for Biosciences, Mukogawa Women's University
  • Toyohara Haruhiko
    Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University
  • Hirata Takashi
    Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University
  • Takayama Eiji
    Faculty of Medicine, National Defense Medical College
  • Mikawa Satoshi
    Division of Applied Life Science, Graduate School of Agriculture, Kyoto University Department of Animal Breeding and Genetics, National Institute of Animal Industry
  • Kioka Noriyuki
    Division of Applied Life Science, Graduate School of Agriculture, Kyoto University
  • Sakaguchi Morihiko
    Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University

書誌事項

タイトル別名
  • cDNA Cloning of Polypeptide Chain Elongation Factor 1α from Medaka <i>Oryzias latipes</i>
  • cDNA Cloning of Polypeptide Chain Elongation Factor 1 アルファ from Medaka Oryzias latipes
  • cDNA Cloning of Polypeptide Chain Elongation Factor 1&alpha; from Medaka <i>Oryzias latipes</i>

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抄録

Polypeptide chain elongation factor 1α (EF1α) was cloned from a liver cDNA library of medaka Orizias latipes. The analysis of the clone containing 1.6kbp DNA revealed that the entire open reading frame of EFla was 1383 bp long. Deduced amino acid sequence of medaka EFlα showed high similarity (more than 87% identity) with those of other vertebrates. Medaka EFlα had one amino acid deletion at the position of 447 amino acid of other EF1αs and unique 17 replacement against those of other vertebrates. Northern hybridization analysis revealed that this EF1α was expressed in all tissues tested.

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