Cloning and characterization of tesk1, a novel spermatogenesis-related gene, in the tongue sole (Cynoglossus semilaevis)

PLoS One. 2014 Oct 1;9(10):e107922. doi: 10.1371/journal.pone.0107922. eCollection 2014.

Abstract

Testis-specific protein kinase 1 (Tesk1) is a serine/threonine kinase with unique structural features. In the present study, we cloned and characterized the tesk1 gene of tongue sole, Cynoglossus semilaevis. The full-length tesk1 cDNA consists of 1,672 nucleotides, encoding a 331 amino acid polypeptide with a characteristic structure composed of an N-terminal kinase domain and a C-terminal proline-rich domain. The tesk1 genomic sequence contains eight exons and seven introns. Real-time quantitative PCR revealed that tesk1 mRNA is expressed predominantly in the testis, though the level of expression varied throughout development. We used in situ hybridization to show that tesk1 mRNA is expressed in the spermatids of males and pseudo-males, but not in triploid males. Our results suggest that tongue sole Tesk1 may play a role in spermatogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromosomes
  • Cloning, Molecular*
  • DNA, Complementary / chemistry
  • DNA, Complementary / genetics
  • Female
  • Fishes / classification
  • Fishes / genetics*
  • Gene Expression
  • Gonads / metabolism
  • Male
  • Molecular Sequence Data
  • Organ Specificity / genetics
  • Phenotype
  • Phylogeny
  • Protein Transport
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Spermatogenesis / genetics*

Substances

  • DNA, Complementary
  • RNA, Messenger

Associated data

  • GENBANK/KF939086

Grants and funding

This work received funding from State 863 High-Technology R&D Project of China (2012AA10A403-2, 2012AA092203), National Nature Science Foundation of China (31130057, 31472269) and Taishan Scholar Project Fund of Shandong of China. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.