Label-free quantitative analysis of the casein kinase 2-responsive phosphoproteome of the marine minimal model species Ostreococcus tauri

Thierry Le Bihan, Matthew Hindle, Sarah F Martin, Martin E Barrios-Llerena, Johanna Krahmer, Katalin Kis, Andrew J Millar, Gerben van Ooijen

Research output: Contribution to journalArticlepeer-review

Abstract

Casein Kinase 2 (CK2) is a protein kinase that phosphorylates a plethora of cellular target proteins involved in processes including DNA repair, cell cycle control, and circadian timekeeping. CK2 is functionally conserved across eukaryotes, although the substrate proteins identified in a range of complex tissues are often different. The marine alga Ostreococcus tauri is a unicellular eukaryotic model organism ideally suited to efficiently study generic roles of CK2 in the cellular circadian clock. Overexpression of CK2 leads to a slow circadian rhythm, verifying functional conservation of CK2 in timekeeping. The proteome was analysed in wild-type and CK2-overexpressing algae at dawn and dusk, revealing that differential abundance of the global proteome across the day is largely unaffected by overexpression. However, CK2 activity contributed more strongly to timekeeping at dusk than at dawn. The phosphoproteome of a CK2 overexpression line and cells treated with CK2 inhibitor was therefore analysed and compared to control cells at dusk. We report an extensive catalogue of 447 unique CK2-responsive differential phosphopeptide motifs to inform future studies into CK2 activity in the circadian clock of more complex tissues This article is protected by copyright. All rights reserved.

Original languageEnglish
Pages (from-to)4135–4144
JournalProteomics
Volume15
Issue number23-24
Early online date29 Apr 2015
DOIs
Publication statusPublished - 2015

Keywords

  • Systems Biology
  • Circadian Clocks
  • biological rhythms
  • Protein Kinases
  • Signal Transduction
  • Marine algae

Fingerprint

Dive into the research topics of 'Label-free quantitative analysis of the casein kinase 2-responsive phosphoproteome of the marine minimal model species Ostreococcus tauri'. Together they form a unique fingerprint.

Cite this