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Molecular characterization of a troponin i-like protein from the hard tick haemaphysalis longicornis

  • Myungjo You
  • , Xuenan Xuan
  • , Naotoshi Tsuji
  • , Tsugihiko Kamio
  • , Ikuo Igarashi
  • , Hideyuki Nagasawa
  • , Takeshi Mikami
  • , Kozo Fujisaki*
  • *Corresponding author for this work
  • Gifu University
  • Obihiro University of Agriculture and Veterinary Medicine
  • National Agriculture and Food Research Organization

Research output: Contribution to journalJournal articlepeer-review

Abstract

A cDNA expression library prepared from mRNA of Haemaphysalis longicornis (H. longicornis) was screened with a H. longicornis-infested rabbit serum. A cDNA encoding 27/30 kDa proteins was cloned and designated P27/30 gene. The predicted amino acid sequence of the P27/30 gene shows a rather high homology (58% amino acid identities and 11% amino acid similarity) with Drosophila melanogaster troponin I clone E2. H. longicornis P27/30 possesses amino acid sequence of actin-binding domains of troponin I at the amino acid residues 128-148, suggesting that H. longicornis P27/30 is a troponin I-like protein. By immunoblot analysis, mouse anti-recombinant P27/30 serum reacted with major constituent protein bands in extracts of adult ticks, and also immunoreacted with muscle, cuticle, gut, and salivary gland in H. longicornis ticks. Moreover, immunohistochemistry using the anti-P27/30 serum showed a strong reactivity in muscle, suggesting that native P27/30 is expressed abundantly in that tissue.

Original languageEnglish
Pages (from-to)67-73
Number of pages7
JournalInsect Biochemistry and Molecular Biology
Volume32
Issue number1
DOIs
StatePublished - 2001

Keywords

  • Haemaphysalis longicornis
  • Tick
  • Troponin I

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