Cloning and characterization of testis-specific tektin in Bombyx mori

Atsuko Ota, Takahiro Kusakabe*, Yasushi Sugimoto, Masateru Takahashi, Yumiko Nakajima, Yutaka Kawaguchi, Katsumi Koga

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

A testis-specific cDNA library of Bombyx mori was constructed by an mRNA subtraction technique. Several clones were randomly selected and determined for their nucleotide sequences. One of them, designated as BmTST, contained a 3′-part of an open reading frame homologous to tektin, the protein known to form filamentous polymers in the walls of ciliary and flagellar microtubules. Also isolated was a genomic fragment, which contains the 5′-part of the coding sequence of BmTST and its promoter region. As a whole, the complete open reading frame was found to encode 508 amino acid residues, whose sequence had 28, 28 and 30% identities with the Strongylocentrotus purpuratus tektins A1, B1 and C1, respectively. Expression analysis by reverse transcription polymerase chain reaction with the cDNA and Western blotting with a polyclonal antibody indicated that the BmTST gene was expressed specifically in the testis during sperm maturation. The protein was immunologically detected exclusively in the fraction expected to contain the 9+2 flagellar axonemes of sperms. We infer that the BmTst protein is possibly involved in the spermatogenesis of B. mori.

Original languageEnglish (US)
Pages (from-to)371-382
Number of pages12
JournalComparative Biochemistry and Physiology - B Biochemistry and Molecular Biology
Volume133
Issue number3
DOIs
StatePublished - Nov 1 2002

Keywords

  • Bombyx mori
  • Expression analysis
  • Promoter
  • Spermatogenesis
  • Tektin
  • Testis specific gene
  • cDNA cloning
  • mRNA subtraction

ASJC Scopus subject areas

  • Biochemistry
  • Physiology

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