ERK Signaling Regulates Light-Induced Gene Expression via D-Box Enhancers in a Differential, Wavelength-Dependent Manner

PLoS One. 2013 Jun 26;8(6):e67858. doi: 10.1371/journal.pone.0067858. Print 2013.

Abstract

The day-night and seasonal cycles are dominated by regular changes in the intensity as well as spectral composition of sunlight. In aquatic environments the spectrum of sunlight is also strongly affected by the depth and quality of water. During evolution, organisms have adopted various key strategies in order to adapt to these changes, including the development of clocks and photoreceptor mechanisms. These mechanisms enable the detection and anticipation of regular changes in lighting conditions and thereby direct an appropriate physiological response. In teleosts, a growing body of evidence points to most cell types possessing complex photoreceptive systems. However, our understanding of precisely how these systems are regulated and in turn dictate changes in gene expression remains incomplete. In this manuscript we attempt to unravel this complexity by comparing the effects of two specific wavelengths of light upon signal transduction and gene expression regulatory mechanisms in zebrafish cells. We reveal a significant difference in the kinetics of light-induced gene expression upon blue and red light exposure. Importantly, both red and blue light-induced gene expression relies upon D-box enhancer promoter elements. Using pharmacological and genetic approaches we demonstrate that the ERK/MAPK pathway acts as a negative regulator of blue but not red light activated transcription. Thus, we reveal that D-box-driven gene expression is regulated via ERK/MAPK signaling in a strongly wavelength-dependent manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gene Expression Regulation / radiation effects*
  • Light*
  • MAP Kinase Signaling System / genetics*
  • Mitogen-Activated Protein Kinases / metabolism*
  • Promoter Regions, Genetic / genetics
  • Regulatory Sequences, Nucleic Acid / genetics*
  • Signal Transduction / radiation effects
  • Zebrafish / genetics*
  • Zebrafish / growth & development

Substances

  • Mitogen-Activated Protein Kinases

Grants and funding

This work was supported by the Karlsruhe Institute of Technology (KIT, Germany) through the Helmholtz funding programme: BioInterfaces (to NSF, DV). FJS-V received financial support from SENECA (08743/PI/08) and MINECO (CSD2007-0002 and AGL2010-22139-c03-01) co-funded by FEDER. PM, CP and IHC were supported by funding by the BioInterfaces programme. JFL-O was supported by a postdoctoral fellowship from Fundacion Seneca (Murcia Spain). MLI was supported by the Italian percorso ad alta formazione Master and Back for the Sardinian region as well as the BioInterfaces programme. NF was supported by a PhD fellowship from the FP7 EU integrated project, ZFHEALTH (HEALTH-F4-2010-242048). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.