4.6 Article

Genome-wide identification and expression analysis of the SNARE genes in Foxtail millet (Setaria italica) reveals its roles in drought stress

期刊

PLANT GROWTH REGULATION
卷 95, 期 3, 页码 355-369

出版社

SPRINGER
DOI: 10.1007/s10725-021-00746-0

关键词

Genome-wide analysis; SNARE; Foxtail millet (Setaria italica); Drought stress

资金

  1. Xinghuacun College of Shanxi University (Shanxi Institute of Brewing Technology and Industry (Preparation)) [XCSXU-KF-202020]
  2. National Key Research and Development Program of China [2020YFD1001401, 2020YFD1001405]
  3. Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi [2019L0104]

向作者/读者索取更多资源

SNARE proteins play important roles in plant growth and development, as well as abiotic stress resistance. This study identified and analyzed 52 SiSNARE genes in foxtail millet, showing tissue-specific expression and differential responses to drought stress in different cultivars. The findings provide valuable genomic information for further research on drought stress response in foxtail millet.
SNARE (soluble-N-ethylmaleimide-sensitive-factor accessory-protein receptor) proteins are important for plant growth and development. Based on their role in membrane fusion, SNARE proteins are involved in abiotic stress resistance. Foxtail millet (Setaria italica) is a widely cultivated crop in Asia with high tolerance to drought stress. The investigation focuses on drought stress-related genes like SNARE will help to reveal the mechanism of foxtail millet drought tolerance. In this study, we identified 52 SiSNARE genes in foxtail millet. Phylogenetic analysis, prediction of conserved motif, and gene structure analysis classified these genes into different groups, including 15 Qa-SiSNARE genes, 10 Qb-SiSNARE genes, 9 Qc-SiSNARE genes, 3 Qb + c-SiSNARE genes, and 15 R-SiSNARE genes. In silico transcript level analysis showed some SiSNAREs were tissue or development stage-specific expressed. Two cultivars of foxtail millet, Jingu21 and Longgu16, showed different phenotypes under drought stress. We detected the expression of 52 SiSNARE genes in these two cultivars under drought stress. There were 15 SiSNARE genes up-regulated and 3 genes down-regulated after drought stress in both two cultivars. We also found 6 SiSNARE genes were specifically altered under stress in cultivar Jingu21, which showed better drought tolerance. Our results provide genomic information for SiSNARE genes in foxtail millet. Analysis of stress-related gene expression in cultivars with different phenotypes suggests some SiSNARE genes' role in drought stress response. These findings laid a foundation for further SNARE related drought stress research in foxtail millet.

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