Screening and analysis of soda saline-alkali stress induced up- regulated genes in sugar sorghum

Abstract

Soil salinization severely constrains the growth of crops, which ultimately leads to reduced yields. Because Sorghum dochna (common name sugar sorghum) has the advantageous properties of excellent salt stress resis- tance, high biomass, and tremendous flexibility for utilization as food, livestock feed, and industrial products, this species holds great potential to be further developed as a primary alternative crop. To elucidate the molecular mechanism that governs sugar sorghum’s adaptation to high salinity environments, we constructed a suppression subtractive hybridization (SSH) cDNA library from sugar sorghum transcripts that contains the soda saline-alkali induced up-regulated genes from the resistant variety M-81E. The SSH cDNA library was screened by using the colony hybridization method, and the ESTs obtained were sequenced and analyzed. A total of 200 EST clones were identified, representing 127 unigenes (6 contigs and 121 singlets). A Blast analysis showed that 48 ESTs (46.6%) have annotated functions in GenBank, 55 ESTs (53.4%) have unknown functions (or encode hypothetical proteins), and 24 ESTs (18.9%) have no blast hits. The majority of the hypothetical ESTs from the cDNA library displayed very high sequence similarity with their homologs found through GenBank. A clustering analysis of the ESTs with known functions indicated that a wide variety of genes were induced during the salt stress treatment. These genes were found to function in photosynthesis, material and energy metabolism (carbohydrates, lipids, amino acids, co-enzymes, ions, etc.), synthesis or maintenance of constituents of the cell wall and cell membrane, signal transduction, transcriptional regulation, and as water channels. This indicates that sugar sorghum tolerance to soda saline-alkali stress results from the coordinated functions of many genes