Stress responsive proteins are actively regulated during rice (Oryza sativa) embryogenesis as indicated by quantitative proteomics analysis

PLoS One. 2013 Sep 18;8(9):e74229. doi: 10.1371/journal.pone.0074229. eCollection 2013.

Abstract

Embryogenesis is the initial step in a plant's life, and the molecular changes that occur during embryonic development are largely unknown. To explore the relevant molecular events, we used the isobaric tags for relative and absolute quantification (iTRAQ) coupled with the shotgun proteomics technique (iTRAQ/Shotgun) to study the proteomic changes of rice embryos during embryogenesis. For the first time, a total of 2 165 unique proteins were identified in rice embryos, and the abundances of 867 proteins were actively changed based on the statistical evaluation of the quantitative MS/MS signals. The quantitative data were then confirmed using multiple reactions monitoring (MRM) and were also supported by our previous study based on two-dimensional gel electrophoresis (2 DE). Using the proteome at 6 days after pollination (DAP) as a reference, cluster analysis of these differential proteins throughout rice embryogenesis revealed that 25% were up-regulated and 75% were down-regulated. Gene Ontology (GO) analysis implicated that most of the up-regulated proteins were functionally categorized as stress responsive, mainly including heat shock-, lipid transfer-, and reactive oxygen species-related proteins. The stress-responsive proteins were thus postulated to play an important role during seed maturation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electrophoresis, Gel, Two-Dimensional
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental*
  • Gene Expression Regulation, Plant*
  • Heat-Shock Proteins / genetics*
  • Heat-Shock Proteins / metabolism
  • Molecular Sequence Annotation
  • Oryza / genetics*
  • Oryza / metabolism
  • Oxidative Stress
  • Plant Proteins / genetics*
  • Plant Proteins / metabolism
  • Proteomics
  • Seeds / genetics*
  • Seeds / metabolism
  • Tandem Mass Spectrometry

Substances

  • Heat-Shock Proteins
  • Plant Proteins

Grants and funding

This work was supported by the National High Technology 863 Research and Development Program of China 2012AA020204,the National Key Basic Research 973 Program of China 2010CB912703, the Natural Science Foundation of China 91131009 and the Guangdong Innovative Research Team Program 2009010016. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.