Brassinosteroids regulate plant growth through distinct signaling pathways in Selaginella and Arabidopsis

PLoS One. 2013 Dec 13;8(12):e81938. doi: 10.1371/journal.pone.0081938. eCollection 2013.

Abstract

Brassinosteroids (BRs) are growth-promoting steroid hormones that regulate diverse physiological processes in plants. Most BR biosynthetic enzymes belong to the cytochrome P450 (CYP) family. The gene encoding the ultimate step of BR biosynthesis in Arabidopsis likely evolved by gene duplication followed by functional specialization in a dicotyledonous plant-specific manner. To gain insight into the evolution of BRs, we performed a genomic reconstitution of Arabidopsis BR biosynthetic genes in an ancestral vascular plant, the lycophyte Selaginella moellendorffii. Selaginella contains four members of the CYP90 family that cluster together in the CYP85 clan. Similar to known BR biosynthetic genes, the Selaginella CYP90s exhibit eight or ten exons and Selaginella produces a putative BR biosynthetic intermediate. Therefore, we hypothesized that Selaginella CYP90 genes encode BR biosynthetic enzymes. In contrast to typical CYPs in Arabidopsis, Selaginella CYP90E2 and CYP90F1 do not possess amino-terminal signal peptides, suggesting that they do not localize to the endoplasmic reticulum. In addition, one of the three putative CYP reductases (CPRs) that is required for CYP enzyme function co-localized with CYP90E2 and CYP90F1. Treatments with a BR biosynthetic inhibitor, propiconazole, and epi-brassinolide resulted in greatly retarded and increased growth, respectively. This suggests that BRs promote growth in Selaginella, as they do in Arabidopsis. However, BR signaling occurs through different pathways than in Arabidopsis. A sequence homologous to the Arabidopsis BR receptor BRI1 was absent in Selaginella, but downstream components, including BIN2, BSU1, and BZR1, were present. Thus, the mechanism that initiates BR signaling in Selaginella seems to differ from that in Arabidopsis. Our findings suggest that the basic physiological roles of BRs as growth-promoting hormones are conserved in both lycophytes and Arabidopsis; however, different BR molecules and BRI1-based membrane receptor complexes evolved in these plants.

MeSH terms

  • Amino Acid Sequence
  • Arabidopsis / genetics
  • Arabidopsis / growth & development
  • Arabidopsis / metabolism*
  • Arabidopsis Proteins / classification
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Brassinosteroids / biosynthesis
  • Brassinosteroids / pharmacology*
  • DNA-Binding Proteins
  • Exons
  • Gene Expression Regulation, Developmental
  • Gene Expression Regulation, Plant*
  • Isoenzymes / classification
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Molecular Sequence Data
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Phosphoprotein Phosphatases / genetics
  • Phosphoprotein Phosphatases / metabolism
  • Phylogeny
  • Plant Growth Regulators / biosynthesis
  • Plant Growth Regulators / pharmacology*
  • Protein Kinases / genetics
  • Protein Kinases / metabolism
  • Selaginellaceae / genetics
  • Selaginellaceae / growth & development
  • Selaginellaceae / metabolism*
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Signal Transduction*
  • Species Specificity
  • Steroid Hydroxylases / classification
  • Steroid Hydroxylases / genetics
  • Steroid Hydroxylases / metabolism*
  • Steroids, Heterocyclic / pharmacology*
  • Triazoles

Substances

  • Arabidopsis Proteins
  • BZR1 protein, Arabidopsis
  • Brassinosteroids
  • DNA-Binding Proteins
  • Isoenzymes
  • Nuclear Proteins
  • Plant Growth Regulators
  • Steroids, Heterocyclic
  • Triazoles
  • propiconazole
  • CPD protein, Arabidopsis
  • Steroid Hydroxylases
  • Protein Kinases
  • BIN2 protein, Arabidopsis
  • BRI1 protein, Arabidopsis
  • BSU1 protein, Arabidopsis
  • Phosphoprotein Phosphatases
  • brassinolide

Grants and funding

This research was supported, in part, by grants from the Next-Generation BioGreen 21 Program (Plant Molecular Breeding Center No. PJ008051), Cooperative Research Program for Agriculture Science & Technology Development (Project No. PJ906910), funded by the Rural Development Administration (to S.C.); Technology Development Program (110033-5) for Agriculture and Forestry, Ministry for Food, Agriculture, Forestry and Fisheries, Republic of Korea (to S.C.); the BK21 Research Fellowships (to J.C.), funded by the Ministry of Education, Republic of Korea; and a Grant-in-Aid for Scientific Research (B) from the Ministry of Education, Culture, Sports, Science and Technology of Japan (19380069 and 23380066 to S.F.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.