[Cloning of HAL1 gene and characterization for salt tolerance tomato]

Sheng Wu Gong Cheng Xue Bao. 2001 Nov;17(6):658-62.
[Article in Chinese]

Abstract

The HAL1 gene was cloned by PCR strategy and confirmed by sequencing. Its open read frame is 879 bp, encoding a peptide of 294 amino acids (32 kD Protein). A chimaeric construct of HAL1 and Npt II (neomycin phosphotransferase II) was constructed and introduced into commercial cultivars of tomato (Zhong SU No. 5: Lycopersicon escullentum) by Agrobacterium tumefacien-mediated gene transformation. Transformants were selected for their ability to grow and root on media containing kanamycin. Transformation was confirmed by analysis of PCR, Southern blot and RT-PCR. The salt tolerance of transgenic tomato is evaluated by comparing the fresh weight, dry weight, Na+, K+ content of transgenic tomato and control tomato. It is concluded that the over-expressing of HAL1 in tomato could enhance the salt tolerance of the transgenic tomato.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cloning, Molecular
  • Fungal Proteins / genetics*
  • Fungal Proteins / physiology
  • Intracellular Signaling Peptides and Proteins
  • Kanamycin Kinase / genetics
  • Plants, Genetically Modified / genetics
  • Plants, Genetically Modified / physiology
  • Recombinant Fusion Proteins / genetics*
  • Recombinant Fusion Proteins / physiology
  • Saccharomyces cerevisiae Proteins*
  • Sodium Chloride / metabolism*
  • Solanum lycopersicum / genetics
  • Solanum lycopersicum / physiology*
  • Transformation, Genetic
  • Yeasts / genetics

Substances

  • Fungal Proteins
  • HAL1 protein, S cerevisiae
  • Intracellular Signaling Peptides and Proteins
  • Recombinant Fusion Proteins
  • Saccharomyces cerevisiae Proteins
  • Sodium Chloride
  • Kanamycin Kinase