Insertion of a specific fungal 3'-phosphoadenosine-5'-phosphatase motif into a plant homologue improves halotolerance and drought tolerance of plants

PLoS One. 2013 Dec 9;8(12):e81872. doi: 10.1371/journal.pone.0081872. eCollection 2013.

Abstract

Soil salinity and drought are among the most serious agricultural and environmental problems of today. Therefore, investigations of plant resistance to abiotic stress have received a lot of attention in recent years. In this study, we identified the complete coding sequence of a 3'-phosphoadenosine-5'-phosphatase protein, ApHal2, from the halotolerant yeast Aureobasidium pullulans. Expression of the ApHAL2 gene in a Saccharomyces cerevisiae hal2 mutant complemented the mutant auxotrophy for methionine, and rescued the growth of the hal2 mutant in media with high NaCl concentrations. A 21-amino-acids-long region of the ApHal2 enzyme was inserted into the Arabidopsis thaliana homologue of Hal2, the SAL1 phosphatase. The inserted sequence included the META motif, which has previously been implicated in increased sodium tolerance of the Hal2 homologue from a related fungal species. Transgenic Arabidopsis plants overexpressing this modified SAL1 (mSAL1) showed improved halotolerance and drought tolerance. In a medium with an elevated salt concentration, mSAL1-expressing plants were twice as likely to have roots in a higher length category in comparison with the wild-type Arabidopsis and with plants overexpressing the native SAL1, and had 5% to 10% larger leaf surface area under moderate and severe salt stress, respectively. Similarly, after moderate drought exposure, the mSAL1-expressing plants showed 14% increased dry weight after revitalisation, with no increase in dry weight of the wild-type plants. With severe drought, plants overexpressing native SAL1 had the worst rehydration success, consistent with the recently proposed role of SAL1 in severe drought. This was not observed for plants expressing mSAL1. Therefore, the presence of this fungal META motif sequence is beneficial under conditions of increased salinity and moderate drought, and shows no drawbacks for plant survival under severe drought. This demonstrates that adaptations of extremotolerant fungi should be considered as a valuable resource for improving stress-tolerance in plant breeding in the future.

MeSH terms

  • Agrobacterium tumefaciens / genetics
  • Agrobacterium tumefaciens / metabolism
  • Amino Acid Motifs
  • Arabidopsis / drug effects
  • Arabidopsis / enzymology
  • Arabidopsis / genetics*
  • Arabidopsis Proteins / chemistry*
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism
  • Droughts
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Fungal Proteins / chemistry*
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Models, Molecular
  • Molecular Sequence Data
  • Nucleotidases / chemistry*
  • Nucleotidases / genetics
  • Nucleotidases / metabolism
  • Phosphoric Monoester Hydrolases
  • Plants, Genetically Modified
  • Protein Engineering
  • Protein Structure, Tertiary
  • Saccharomycetales / drug effects
  • Saccharomycetales / enzymology
  • Saccharomycetales / genetics*
  • Salinity
  • Salt Tolerance / genetics*
  • Sequence Alignment
  • Sodium Chloride / pharmacology
  • Transformation, Genetic

Substances

  • Arabidopsis Proteins
  • Fungal Proteins
  • Sodium Chloride
  • Nucleotidases
  • Phosphoric Monoester Hydrolases
  • inositol-1,4-bisphosphate 1-phosphatase
  • bisphosphoadenylate 3'-nucleotidase

Grants and funding

The authors acknowledge the financial support from the state budget by the Slovenian Research Agency (grants no. J4-2022, P1-170, P4-0165, Infrastructural Centre Mycosmo, MRIC UL, and postdoctoral project Z4-5531 to CG) and COST network FA0804. The scientific work was partly financed via operation “Centre of excellence for integrated approaches in chemistry and biology of proteins” number OP13.1.1.2.02.0005, financed by European regional development fund (85% share of financing) and by the Slovenian Ministry of higher education, science and technology (15% share of financing). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.