Phototropins Mediate Chloroplast Movement in Phalaenopsis aphrodite (Moth Orchid)

Plant Cell Physiol. 2019 Oct 1;60(10):2243-2254. doi: 10.1093/pcp/pcz116.

Abstract

Chloroplast movement is important for plants to avoid photodamage and to perform efficient photosynthesis. Phototropins are blue light receptors in plants that function in chloroplast movement, phototropism, stomatal opening, and they also affect plant growth and development. In this study, full-length cDNAs of two PHOTOTROPIN genes, PaPHOT1 and PaPHOT2, were cloned from a moth orchid Phalaenopsis aphrodite, and their functions in chloroplast movement were investigated. Phylogenetic analysis showed that PaPHOT1 and PaPHOT2 orthologs were highly similar to PHOT1 and PHOT2 of the close relative Phalaenopsis equestris, respectively, and clustered with monocots PHOT1 and PHOT2 orthologs, respectively. Phalaenopsis aphrodite expressed a moderate level of PaPHOT1 under low blue light of 5 μmol�m-2�s-1 (BL5) and a high levels of PaPHOT1 at >BL100. However, PaPHOT2 was expressed at low levels at <BL50 but expressed at high levels at > BL100. Analysis of light-induced chloroplast movements using the SPAD method indicated that orchid accumulated chloroplasts at <BL10. The chloroplast avoidance response was detectable at >BL25 and significant chloroplast avoidance movement was observed at >BL100. Virus-induced gene silencing of PaPHOTs in orchids showed decreased gene expression of PaPHOTs and reduced both chloroplast accumulation and avoidance responses. Heterologous expression of PaPHOT1 in Arabidopsis phot1phot2 double mutant recovered chloroplast accumulation response at BL5, but neither PaPHOT1 nor PaPHOT2 was able to restore mutant chloroplast avoidance at BL100. Overall, this study showed that phototropins mediate chloroplast movement in Phalaenopsis orchid is blue light-dependent but their function is slightly different from Arabidopsis which might be due to gene evolution.

Keywords: Blue-light receptors; Chloroplast movement; In situ hybridization; Moth orchid; Photodamage; Virus-induced gene silencing.

MeSH terms

  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism
  • Chloroplasts / metabolism
  • Chloroplasts / radiation effects
  • DNA, Complementary / genetics
  • Gene Expression
  • Gene Silencing
  • In Situ Hybridization
  • Light
  • Mutation
  • Orchidaceae / genetics
  • Orchidaceae / physiology*
  • Orchidaceae / radiation effects
  • Photosynthesis
  • Phototropins / genetics
  • Phototropins / metabolism*
  • Phototropism*
  • Phylogeny
  • Plant Leaves / genetics
  • Plant Leaves / physiology
  • Plant Leaves / radiation effects
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Plants, Genetically Modified
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism

Substances

  • Arabidopsis Proteins
  • DNA, Complementary
  • PHOT2 protein, Arabidopsis
  • Phototropins
  • Plant Proteins
  • NPH1 protein, Arabidopsis
  • Protein Serine-Threonine Kinases