Cloning of two contrasting high-affinity sulfate transporters from tomato induced by low sulfate and infection by the vascular pathogen Verticillium dahliae

Planta. 2003 Nov;218(1):58-64. doi: 10.1007/s00425-003-1085-5. Epub 2003 Aug 23.

Abstract

Two cDNAs, LeST1-1 (AF347613) and LeST1-2 (AF347614), encoding sulfate transporters have been cloned from tomato (Lycopersicon esculentum Mill.) by reverse transcription-polymerase chain reaction and their expression characterised. Sharing 76% identity at the amino acid level, the transporters are phylogenetically associated with the Group-1, high-affinity plant sulfate transporters. Both were shown to have high affinity for sulfate by uptake kinetic analysis using a yeast (Saccharomyces cerevisiae) sulfate-transporter mutant. Km values of 11.5 microM and 9.8 microM were calculated for LeST1-1 and LeST1-2, respectively, the same order of magnitude as those previously reported for several other Group-1 high-affinity sulfate transporters. In situ hybridisation to S-deficient tomato roots showed LeST1-1 to be expressed in the epidermis and pericycle, whereas LeST1-2 expression was located to the epidermis only. Northern analysis shows that the mRNA abundances of both LeST1-1 and LeST1-2 are upregulated in the root in response to sulfate deprivation. LeST1-1 is specifically expressed in root tissue, a characteristic of Group-1 sulfate transporters. LeST1-2, however, was also detected in tomato leaves and stems and is upregulated and expressed to a similar extent in these tissues under conditions of sulfate deprivation. Induction of LeST1-2 expression was also observed in the vascular tissues of a resistant line of tomato infected with the vascular wilt pathogen Verticillium dahliae.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Biological Transport
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Cloning, Molecular / methods
  • DNA Primers
  • In Situ Hybridization
  • Kinetics
  • Membrane Transport Proteins*
  • Plant Diseases / microbiology
  • Plant Roots / metabolism
  • Plant Roots / microbiology
  • Solanum lycopersicum / genetics*
  • Solanum lycopersicum / metabolism
  • Solanum lycopersicum / microbiology*
  • Sulfate Transporters
  • Sulfates / metabolism
  • Transcription, Genetic / genetics*
  • Verticillium / pathogenicity*

Substances

  • Carrier Proteins
  • DNA Primers
  • Membrane Transport Proteins
  • SLC26A4 protein, human
  • Sulfate Transporters
  • Sulfates