Overexpression of Medicago sativa LEA4-4 can improve the salt, drought, and oxidation resistance of transgenic Arabidopsis

PLoS One. 2020 Jun 4;15(6):e0234085. doi: 10.1371/journal.pone.0234085. eCollection 2020.

Abstract

Late embryogenesis abundant (LEA) proteins are widely involved in many adverse conditions among plants. In this study, we isolated a LEA4 gene from alfalfa (Medicago sativa L.) termed MsLEA4-4 via a homology cloning strategy. MsLEA4-4 encodes 166 amino acids, and the structural analysis showed that the gene contained five repeating TAQAAKEKTQQ amino acid motifs. There were a large number of α-helix in MsLEA4-4, and belongs to hydrophilic amino acid. Subcellular localization analysis showed that MsLEA4-4 was localized in the nucleus. The MsLEA4-4 promoter consisted of G-box and A-box elements, abscisic acid-responsive elements (ABREs), photo regulation and photoperiodic-controlling cis-acting elements, and endosperm expression motifs. The MsLEA4-4 overexpressing in Arabidopsis conferred late-germination phenotypes. Resistance of the overexpressed plants to abiotic stress significantly outperformed the wild-type (WT) plants. Under salt stress and abscisic acid treatment, with more lateral roots and higher chlorophyll content, the overexpressed plants has a higher survival rate measured against WT. Compared to those in the WT plants, the levels of soluble sugar and the activity of various antioxidant enzymes were elevated in the overexpressed plants, whereas the levels of proline and malondialdehyde were significantly reduced. The expression levels of several genes such as ABF3, ABI5, NCED5, and NCED9 increased markedly in the overexpressed plants compared to the WT under osmotic stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Arabidopsis / genetics*
  • Arabidopsis / growth & development
  • Arabidopsis / metabolism
  • Arabidopsis / physiology*
  • Base Sequence
  • Cloning, Molecular
  • Droughts*
  • Gene Expression
  • Germination
  • Medicago sativa / genetics*
  • Osmotic Pressure
  • Oxidative Stress / genetics*
  • Plant Proteins / chemistry
  • Plant Proteins / genetics*
  • Promoter Regions, Genetic / genetics
  • Salt Stress / genetics*

Substances

  • Plant Proteins

Grants and funding

The work was supported by a grant from the Special Funds for the Technical System of the Modern Agricultural Industry of China (CARS-34), by the Species Resources Conservation of China (2130135) and by the Key Research and Development Projects of ShanXi (201703D211002-9-2).