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Genome-Wide Analysis and Expression Profiling of DUF668 Genes in Glycine max under Salt Stress

文献类型: 外文期刊

作者: Zaynab, Madiha 1 ; Sharif, Yasir 3 ; Xu, Zhaoshi 4 ; Fiaz, Sajid 5 ; Al-Yahyai, Rashid 6 ; Yadikar, Hamad. A. 7 ; Al Kashgry, Najla Amin T. 8 ; Qari, Sameer H. 9 ; Sadder, Monther 10 ; Li, Shuangfei 2 ;

作者机构: 1.Shenzhen Univ, Coll Phys & Optoelect Engn, Shenzhen 518060, Peoples R China

2.Shenzhen Univ, Coll Life Sci & Oceanog, Shenzhen Key Lab Marine Bioresource & Ecoenvironm, Shenzhen 518060, Peoples R China

3.Fujian Agr & Forestry Univ, Coll Plant Protect, Fuzhou 350002, Peoples R China

4.Chinese Acad Agr Sci, Inst Crop Sci,Minist Educ, Key Lab Biol & Genet Improvement Triticeae Crops, Natl Key Facil Crop Gene Resources & Genet Improve, Beijing 100081, Peoples R China

5.Univ Haripur, Dept Plant Breeding & Genet, Haripur 22620, Pakistan

6.Sultan Qaboos Univ, Coll Agr & Marine Sci, Dept Plant Sci, POB 34, Muscat 123, Oman

7.Kuwait Univ, Fac Sci, Dept Biol Sci, POB 5969, Safat 13060, Kuwait

8.Taif Univ, Coll Sci, Dept Biol, POB 11099, Taif 21944, Saudi Arabia

9.Umm Al Qura Univ, Al Jumum Univ Coll, Dept Biol, Mecca 21955, Saudi Arabia

10.Univ Jordan, Sch Agr, Amman 11942, Jordan

关键词: phytohormones; miRNAs; gene expression; abiotic stress; phylogeny; duplication

期刊名称:PLANTS-BASEL ( 影响因子:4.5; 五年影响因子:4.8 )

ISSN:

年卷期: 2023 年 12 卷 16 期

页码:

收录情况: SCI

摘要: The DUF668 gene performs a critical role in mitigating the impact of abiotic stress factors. In this study, we identified 30 DUF668 genes in a soybean genome, distributed across fifteen chromosomes. The phylogenetic analysis classified the DUF668 genes into three groups (group I, group II, and group III). Interestingly, gene structure analysis illustrated that several GmDUF668 genes were without introns. Furthermore, the subcellular localization results suggested that GmDUF668 proteins were present in the nucleus, mitochondria, cytoplasm, and plasma membrane. GmDUF668 promoters were analyzed in silico to gain insight into the presence of regulatory sequences for TFs binding. The expression profiling illustrated that GmDUF668 genes showed expression in leaves, roots, nodules, and flowers. To investigate their response to salt stress, we utilized the RNA sequencing data of GmDUF668 genes. The results unveiled that GmDUF668-8, GmDUF668-20, and GmDUF668-30 genes were upregulated against salt stress treatment. We further validated these findings using qRT-PCR analysis. These findings provide a scientific basis to explore the functions of GmDUF668 genes against different stress conditions.

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