Transcriptomic profiling and analysis of differentially expressed genes in asparagus bean (Vigna unguiculata ssp. sesquipedalis) under salt stress

被引:13
|
作者
Pan, Lei [1 ,2 ,3 ]
Yu, Xiaolu [1 ]
Shao, Jingjie [1 ]
Liu, Zhichao [2 ,3 ]
Gao, Tong [1 ]
Zheng, Yu [4 ]
Zeng, Chen [2 ,3 ]
Liang, Chengzhi [5 ]
Chen, Chanyou [1 ]
机构
[1] Jianghan Univ, Sch Life Sci, Hubei Prov Engn Res Ctr Legume Plants, Wuhan, Hubei, Peoples R China
[2] George Washington Univ, Computat Biol Inst, Washington, DC 20052 USA
[3] George Washington Univ, Dept Phys, Ctr Biomol Sci, Washington, DC 20052 USA
[4] Jianghan Univ, Inst Interdisciplinary Res, Wuhan, Hubei, Peoples R China
[5] Chinese Acad Sci, Inst Genet & Dev, Beijing, Peoples R China
来源
PLOS ONE | 2019年 / 14卷 / 07期
基金
中国国家自然科学基金;
关键词
ZINC-FINGER PROTEINS; HIGH-SALINITY STRESS; ABIOTIC STRESS; ARABIDOPSIS-THALIANA; FUNCTIONAL GENOMICS; L; WALP; TOLERANCE; CROP; DROUGHT; COWPEA;
D O I
10.1371/journal.pone.0219799
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Asparagus bean (Vigna unguiculata ssp. sesquipedalis) is a warm season legume which is widely distributed over subtropical regions and semiarid areas. It is mainly grown as a significant protein source in developing countries. Salinity, as one of the main abiotic stress factors, constrains the normal growth and yield of asparagus bean. This study used two cultivars (a salt-sensitive genotype and a salt-tolerant genotype) under salt stress vs. control to identify salt-stress-induced genes in asparagus bean using RNA sequencing. A total of 692,086,838 high-quality clean reads, assigned to 121,138 unigenes, were obtained from control and salt-treated libraries. Then, 216 root-derived DEGs (differentially expressed genes) and 127 leaf-derived DEGs were identified under salt stress between the two cultivars. Of these DEGs, thirteen were assigned to six transcription factors (TFs), including AP2/EREBP, CCHC(Zn), C2H2, WRKY, WD40-like and LIM. GO analysis indicated four DEGs might take effects on the "oxidation reduction", "transport" and "signal transduction" process. Moreover, expression of nine randomly-chosen DEGs was verified by quantitative real-time-PCR (qRT-PCR) analysis. Predicted function of the nine tested DEGs was mainly involved in the KEGG pathway of cation transport, response to osmotic stress, and phosphorelay signal transduction system. A salt-stress-related pathway of "SNARE interactions in vesicular transport" was concerned. As byproducts, 15, 321 microsatellite markers were found in all the unigenes, and 17 SNP linked to six salt-stress induced DEGs were revealed. These candidate genes provide novel insights for understanding the salt tolerance mechanism of asparagus bean in the future.
引用
收藏
页数:23
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