Current Genomics

Author(s): Min Li, Chunmei Yu, Yaoyi Wang, Wentao Li, Ying Wang, Yun Yang, Huihui Liu, Yujuan Li, Feng Tan and Jian Zhang

DOI: 10.2174/138920291505141106102544

Cloning and Characterisation of Two H+ Translocating Organic Pyrophosphatase Genes in Salix and Their Expression Differences in Two Willow Varieties with Different Salt Tolerances

Page: [341 - 348] Pages: 8

  • * (Excluding Mailing and Handling)

Abstract

Willows are one of the most important tree species for landscaping, biofuel and raw timber. Screening salttolerant willow varieties is an effective approach to balance wood supply and demand. However, more salt-tolerant willow varieties are required and little is known regarding the mechanism of salt tolerance at the gene expression level. In this paper, two willow varieties were studies in terms of their differences in salt-tolerances and mechanism of salt tolerance at the level of VP1 gene expression. The results showed that Salix L0911 (L0911) had higher biomass than Salix matsudana (SM), and salt injuries were less severe in L0911 than in SM. The activities of peroxidase and superoxide dismutase, as well as the contents of soluble protein and proline, were higher in L0911 than in SM, whereas the contents of Na+ and K+, as well as the Na+/K+ ratio, were lower in L0911 than in SM. Two VP1 genes (VP1.1 and VP1.2) cloned in L0911 and SM had similar sequences and structures. VP1.1 and VP1.2 belonged to different subgroups. Total expression levels of the VP1.1 gene in both roots and leaves of L0911 were higher than that in SM under normal conditions. Under salt stress, expression of VP1 in SM roots initially increased and then decreased, whereas the expression of VP1 in leaves of L0911 and SM, as well as in roots of L0911, decreased with increasing salt concentrations. This study increased our understanding of the salt-tolerance mechanism of willow and may facilitate the selection of salt-tolerant willow resources.

Keywords: Willow, VP1 gene, Salt tolerance, Gene expression, Phylogenetic analysis.

Graphical Abstract