Digital gene expression tag profiling analysis of the gene expression patterns regulating the early stage of mouse spermatogenesis

PLoS One. 2013;8(3):e58680. doi: 10.1371/journal.pone.0058680. Epub 2013 Mar 15.

Abstract

Detailed characterization of the gene expression patterns in spermatogonia and primary spermatocytes is critical to understand the processes which occur prior to meiosis during normal spermatogenesis. The genome-wide expression profiles of mouse type B spermatogonia and primary spermatocytes were investigated using the Solexa/Illumina digital gene expression (DGE) system, a tag based high-throughput transcriptome sequencing method, and the developmental processes which occur during early spermatogenesis were systematically analyzed. Gene expression patterns vary significantly between mouse type B spermatogonia and primary spermatocytes. The functional analysis revealed that genes related to junction assembly, regulation of the actin cytoskeleton and pluripotency were most significantly differently expressed. Pathway analysis indicated that the Wnt non-canonical signaling pathway played a central role and interacted with the actin filament organization pathway during the development of spermatogonia. This study provides a foundation for further analysis of the gene expression patterns and signaling pathways which regulate the molecular mechanisms of early spermatogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Computational Biology
  • Databases, Nucleic Acid
  • Fibroblast Growth Factor 7 / genetics
  • Fibroblast Growth Factor 7 / metabolism
  • Fibroblast Growth Factors / genetics
  • Fibroblast Growth Factors / metabolism
  • Focal Adhesions / genetics
  • Gene Expression Profiling*
  • Gene Expression Regulation, Developmental*
  • Gene Library
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mitogen-Activated Protein Kinases
  • Reproducibility of Results
  • Signal Transduction
  • Spermatocytes / metabolism
  • Spermatogenesis / genetics*
  • Spermatogenesis / physiology
  • Wnt Proteins / genetics
  • Wnt Proteins / metabolism
  • rac GTP-Binding Proteins / genetics
  • rac GTP-Binding Proteins / metabolism

Substances

  • Membrane Proteins
  • Sfrp2 protein, mouse
  • Wnt Proteins
  • Fibroblast Growth Factor 7
  • fibroblast growth factor 13
  • Fibroblast Growth Factors
  • Mitogen-Activated Protein Kinases
  • rac GTP-Binding Proteins

Grants and funding

This work was supported by grants from the National Natural Science Foundation of China (Nos. 81170616; 81072093; 30671092), the Natural Science Foundation of Hebei Province (C2009001260; C2012401039) and the Scientific and Technical Supporting Programs of Hebei Province (No. 10276109D). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.