Molecular Characterization and Co-expression Analysis of the SnRK2 Gene Family in Sugarcane (Saccharum officinarum L.)

被引:14
|
作者
Li, Changning [1 ,2 ]
Nong, Qian [2 ]
Xie, Jinlan [2 ]
Wang, Zeping [1 ,2 ]
Liang, Qiang [2 ]
Solanki, Manoj Kumar [2 ]
Malviya, Mukesh Kumar [2 ]
Liu, Xiaoyan [2 ]
Li, Yijie [2 ]
Htun, Reemon [2 ]
Wei, Jiguang [1 ]
Li, Yangrui [1 ,2 ]
机构
[1] Guangxi Univ, Coll Agr, State Key Lab Conservat & Utilizat Subtrop Agrobi, Nanning 530004, Guangxi, Peoples R China
[2] Chinese Acad Agr Sci, Key Lab Sugarcane Biotechnol & Genet Improvement, Guangxi Key Lab Sugarcane Genet Improvement, Minist Agr,Sugarcane Res Ctr, Nanning 530007, Guangxi, Peoples R China
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
基金
中国博士后科学基金;
关键词
GENOME-WIDE IDENTIFICATION; ABA SIGNAL-TRANSDUCTION; TRITICUM-AESTIVUM L; PROTEIN-KINASE; DROUGHT TOLERANCE; OSMOTIC-STRESS; EXPRESSION; WHEAT; ARABIDOPSIS; ACTIVATION;
D O I
10.1038/s41598-017-16152-4
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
In plants, both abscisic acid (ABA) dependent and independent pathways form the basis for the response to environmental stresses. Sucrose non-fermenting 1-related protein kinase 2 (SnRK2) plays a central role in plant stress signal transduction. However, complete annotation and specific expression patterns of SnRK2s in sugarcane remain unclear. For the present study, we performed a full-length cDNA library survey of sugarcane, thus identifying ten SoSnRK2 genes via phylogenetic, local BLAST methods, and various bioinformatics analyses. Phylogenetic analysis indicated division of SoSnRK2 genes into three subgroups, similar to other plant species. Gene structure comparison with Arabidopsis suggested a unique evolutionary imprint of the SnRK2 gene family in sugarcane. Both sequence alignment and structural annotation provided an overview of the conserved N-terminal and variations of the C-terminal, suggesting functional divergence. Transcript and transient expression assays revealed SoSnRK2s to be involved in the responses to diverse stress signals, and strong ABA induction of SoSnRK2s in subgroup III. Co-expression network analyses indicated the existence of both conserved and variable biological functions among different SoSnRK2s members. In summary, this comprehensive analysis will facilitate further studies of the SoSnRK2 family and provide useful information for the functional validation of SoSnRK2s.
引用
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页数:12
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