Physiological and genetic characterization of end-of-day far-red light response in maize seedlings

Plant Physiol. 2010 Sep;154(1):173-86. doi: 10.1104/pp.110.159830. Epub 2010 Jul 28.

Abstract

Developmental responses associated with end-of-day far-red light (EOD-FR) signaling were investigated in maize (Zea mays subspecies mays) seedlings. A survey of genetically diverse inbreds of temperate and tropical/semitropical origins, together with teosinte (Zea mays subspecies parviglumis) and a modern hybrid, revealed distinct elongation responses. A mesocotyl elongation response to the EOD-FR treatment was largely absent in the tropical/semitropical lines, but both hybrid and temperate inbred responses were of the same magnitude as in teosinte, suggesting that EOD-FR-mediated mesocotyl responses were not lost during the domestication or breeding process. The genetic architecture underlying seedling responses to EOD-FR was investigated using the intermated B73 x Mo17 mapping population. Among the different quantitative trait loci identified, two were consistently detected for elongation and responsiveness under EOD-FR, but none were associated with known light signaling loci. The central role of phytochromes in mediating EOD-FR responses was shown using a phytochromeB1 phytochromeB2 (phyB1 phyB2) mutant series. Unlike the coleoptile and first leaf sheath, EOD-FR-mediated elongation of the mesocotyl appears predominantly controlled by gibberellin. EOD-FR also reduced abscisic acid (ABA) levels in the mesocotyl for both the wild type and phyB1 phyB2 double mutants, suggesting a FR-mediated but PHYB-independent control of ABA accumulation. EOD-FR elongation responses were attenuated in both the wild type and phyB1 phyB2 double mutants when a chilling stress was applied during the dark period, concomitant with an increase in ABA levels. We present a model for the EOD-FR response that integrates light and hormonal control of seedling elongation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Abscisic Acid / metabolism
  • Cold Temperature
  • Darkness
  • Gibberellins / pharmacology
  • Inbreeding
  • Light*
  • Models, Biological
  • Mutation / genetics
  • Organ Specificity / drug effects
  • Organ Specificity / genetics
  • Organ Specificity / radiation effects
  • Phytochrome B / metabolism
  • Plant Leaves / drug effects
  • Plant Leaves / metabolism
  • Plant Leaves / radiation effects
  • Quantitative Trait Loci / genetics
  • Seedlings / genetics*
  • Seedlings / growth & development
  • Seedlings / physiology*
  • Seedlings / radiation effects
  • Seeds / drug effects
  • Seeds / genetics
  • Seeds / radiation effects
  • Time Factors
  • Zea mays / genetics*
  • Zea mays / growth & development
  • Zea mays / physiology*
  • Zea mays / radiation effects

Substances

  • Gibberellins
  • Phytochrome B
  • Abscisic Acid
  • gibberellic acid