Molecular cloning and functional characterization of Catharanthus roseus hydroxymethylbutenyl 4-diphosphate synthase gene promoter from the methyl erythritol phosphate pathway

Mol Biol Rep. 2012 May;39(5):5433-47. doi: 10.1007/s11033-011-1343-8. Epub 2011 Dec 13.

Abstract

The Madagascar periwinkle produces monoterpenoid indole alkaloids (MIA) of high interest due to their therapeutical values. The terpenoid moiety of MIA is derived from the methyl erythritol phosphate (MEP) and seco-iridoid pathways. These pathways are regarded as the limiting branch for MIA biosynthesis in C. roseus cell and tissue cultures. In previous studies, we demonstrated a coordinated regulation at the transcriptional and spatial levels of genes from both pathways. We report here on the isolation of the 5'-flanking region (1,049 bp) of the hydroxymethylbutenyl 4-diphosphate synthase (HDS) gene from the MEP pathway. To investigate promoter transcriptional activities, the HDS promoter was fused to GUS reporter gene. Agrobacterium-mediated transformation of young tobacco leaves revealed that the cloned HDS promoter displays a tissue-specific GUS staining restricted to the vascular region of the leaves and limited to a part of the vein that encompasses the phloem in agreement with the previous localization of HDS transcripts in C. roseus aerial organs. Further functional characterizations in stably or transiently transformed C. roseus cells allowed us to identify the region that can be consider as the minimal promoter and to demonstrate the induction of HDS promoter by several hormonal signals (auxin, cytokinin, methyljasmonate and ethylene) leading to MIA production. These results, and the bioinformatic analysis of the HDS 5'-region, suggest that the HDS promoter harbours a number of cis-elements binding specific transcription factors that would regulate the flux of terpenoid precursors involved in MIA biosynthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5' Flanking Region / genetics
  • Acetates / pharmacology
  • Base Sequence
  • Biosynthetic Pathways / drug effects
  • Catharanthus / cytology
  • Catharanthus / drug effects
  • Catharanthus / enzymology*
  • Catharanthus / genetics*
  • Cloning, Molecular
  • Cyclopentanes / pharmacology
  • Cytokinins / pharmacology
  • Enzymes / genetics*
  • Enzymes / metabolism
  • Erythritol / analogs & derivatives*
  • Erythritol / metabolism*
  • Ethylenes / pharmacology
  • Gene Expression Profiling
  • Gene Expression Regulation, Plant / drug effects
  • Genes, Plant / genetics*
  • Glucuronidase / metabolism
  • Molecular Sequence Data
  • Nicotiana / drug effects
  • Nicotiana / genetics
  • Nucleotide Motifs / genetics
  • Organ Specificity / drug effects
  • Organ Specificity / genetics
  • Oxylipins / pharmacology
  • Plant Leaves / drug effects
  • Plant Leaves / enzymology
  • Plant Leaves / genetics
  • Plants, Genetically Modified
  • Promoter Regions, Genetic*
  • Secologanin Tryptamine Alkaloids / metabolism
  • Sequence Analysis, DNA
  • Sequence Deletion / genetics
  • Sugar Phosphates / metabolism*
  • Suspensions
  • Transcription, Genetic / drug effects

Substances

  • 2-C-methylerythritol 4-phosphate
  • Acetates
  • Cyclopentanes
  • Cytokinins
  • Enzymes
  • Ethylenes
  • Oxylipins
  • Secologanin Tryptamine Alkaloids
  • Sugar Phosphates
  • Suspensions
  • hydroxymethylbutenyl 4-diphosphate synthase
  • methyl jasmonate
  • ethylene
  • Glucuronidase
  • Erythritol