Quantitative proteomic analysis of cell cycle of the dinoflagellate Prorocentrum donghaiense (Dinophyceae)

PLoS One. 2013 May 15;8(5):e63659. doi: 10.1371/journal.pone.0063659. Print 2013.

Abstract

Dinoflagellates are the major causative agents of harmful algal blooms in the coastal zone, which has resulted in adverse effects on the marine ecosystem and public health, and has become a global concern. Knowledge of cell cycle regulation in proliferating cells is essential for understanding bloom dynamics, and so this study compared the protein profiles of Prorocentrum donghaiense at different cell cycle phases and identified differentially expressed proteins using 2-D fluorescence difference gel electrophoresis combined with MALDI-TOF-TOF mass spectrometry. The results showed that the synchronized cells of P. donghaiense completed a cell cycle within 24 hours and cell division was phased with the diurnal cycle. Comparison of the protein profiles at four cell cycle phases (G1, S, early and late G2/M) showed that 53 protein spots altered significantly in abundance. Among them, 41 were identified to be involved in a variety of biological processes, e.g. cell cycle and division, RNA metabolism, protein and amino acid metabolism, energy and carbon metabolism, oxidation-reduction processes, and ABC transport. The periodic expression of these proteins was critical to maintain the proper order and function of the cell cycle. This study, to our knowledge, for the first time revealed the major biological processes occurring at different cell cycle phases which provided new insights into the mechanisms regulating the cell cycle and growth of dinoflagellates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Cell Cycle*
  • Dinoflagellida / cytology*
  • Dinoflagellida / metabolism
  • Electrophoresis, Gel, Two-Dimensional / methods
  • Proteomics*
  • Protozoan Proteins / metabolism*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • Protozoan Proteins

Grants and funding

This work was partially supported by research grants from the Ministry of Science and Technology of the People’s Republic of China (Project No. 2010CB428703 and 2011CB111500), the National Natural Science Foundation of China (41230961), the Excellent Group and the Program for New Century Excellent Talents in University to D.-Z. Wang. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.