A Selaginella lepidophylla trehalose-6-phosphate synthase complements growth and stress-tolerance defects in a yeast tps1 mutant

Rodolfo Zentella, José O. Mascorro-Gallardo, Patrick Van Dijck, Jorge Folch-Mallol, Beatriz Bonini, Christophe Van Vaeck, Roberto Gaxiola, Alejandra A. Covarrubias, Jorge Nieto-Sotelo, Johan M. Thevelein, Gabriel Iturriaga

Research output: Contribution to journalArticlepeer-review

148 Scopus citations

Abstract

The accumulation of the disaccharide trehalose in anhydrobiotic organisms allows them to survive severe environmental stress. A plant cDNA, SITPS1, encoding a 109-kD protein, was isolated from the resurrection plant Selaginella lepidophylla, which accumulates high levels of trehalose. Protein-sequence comparison showed that SITPS1 shares high similarity to trehalose-6-phosphate synthase genes from prokaryotes and eukaryotes. SITPS1 mRNA was constitutively expressed in S. lepidophylla. DNA gel-blot analysis indicated that SITPS1 is present as a single-copy gene. Transformation of a Saccharomyces cerevisiae tps1Δ mutant disrupted in the ScTPS1 gene with S. lepidophylla SITPS1 restored growth on fermentable sugars and the synthesis of trehalose at high levels. Moreover, the SITPS1 gene introduced into the tps1Δ mutant was able to complement both deficiencies: sensitivity to sublethal heat treatment at 39°C and induced thermotolerance at 50°C. The osmosensitive phenotype of the yeast tps1Δ mutant grown in NaCl and sorbitol was also restored by the SITPS1 gene. Thus, SITPS1 protein is a functional plant homolog capable of sustaining trehalose biosynthesis and could play a major role in stress tolerance in S. lepidophylla.

Original languageEnglish (US)
Pages (from-to)1473-1482
Number of pages10
JournalPlant Physiology
Volume119
Issue number4
DOIs
StatePublished - Apr 1999
Externally publishedYes

ASJC Scopus subject areas

  • Physiology
  • Genetics
  • Plant Science

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