Identification of a molecular marker for type A spermatogonia by microarray analysis using gonadal cells from pvasa-GFP transgenic rainbow trout (Oncorhynchus mykiss)

Mol Reprod Dev. 2009 Mar;76(3):246-54. doi: 10.1002/mrd.20947.

Abstract

The spermatogonia of fish can be classified as being either undifferentiated type A spermatogonia or differentiated type B spermatogonia. Although type A spermatogonia, which contain spermatogonial stem cells, have been demonstrated to be a suitable material for germ cell transplantation, no molecular markers for distinguishing between type A and type B spermatogonia in fish have been developed to date. We therefore sought to develop a molecular marker for type A spermatogonia in rainbow trout. Using GFP-dependent flow cytometry (FCM), enriched fractions of type A and type B spermatogonia, testicular somatic cells, and primordial germ cells were prepared from rainbow trout possessing the green fluorescent protein (GFP) gene driven by trout vasa regulatory regions (pvasa-GFP rainbow trout). The gene-expression profiles of each cell fraction were then compared with a microarray containing cDNAs representing 16,006 genes from several salmonid species. Genes exhibiting high expression for type A spermatogonia relative to above-mentioned other types of gonadal cells were identified and subjected to RT-PCR and quatitative PCR analysis. Since only the rainbow trout notch1 homologue showed significantly high expression in the type A spermatogonia-enriched fraction, we propose that notch1 may be a useful molecular marker for type A spermatogonia. The combination of GFP-dependent FCM and microarray analysis of pvasa-GFP rainbow trout can therefore be applied to the identification of potentially useful molecular markers of germ cells in fish.

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Biomarkers / metabolism*
  • Expressed Sequence Tags / metabolism
  • Fish Proteins / genetics
  • Fish Proteins / metabolism
  • Flow Cytometry
  • Green Fluorescent Proteins / metabolism
  • In Situ Hybridization, Fluorescence
  • Luminescent Agents / metabolism
  • Male
  • Oligonucleotide Array Sequence Analysis / methods*
  • Oncorhynchus mykiss / genetics
  • Oncorhynchus mykiss / metabolism*
  • Phylogeny
  • Receptor, Notch1 / genetics
  • Receptor, Notch1 / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Spermatogonia / metabolism*
  • Testis / cytology

Substances

  • Biomarkers
  • Fish Proteins
  • Luminescent Agents
  • Receptor, Notch1
  • Green Fluorescent Proteins