The Dendrobium catenatum DcCIPK24 increases drought and salt tolerance of transgenic Arabidopsis

被引:11
作者
Zhang, Tingting [1 ]
Li, Yuxin [1 ]
Kang, Yuqian [1 ]
Wang, Peng [1 ]
Li, Wei [3 ]
Yu, Wengang [1 ]
Wang, Jian [1 ,4 ]
Song, Xiqiang [4 ]
Jiang, Xingyu [2 ]
Zhou, Yang [1 ]
机构
[1] Hainan Univ, Key Lab Qual Regulat Trop Hort Crops Hainan Prov, Hainan Key Lab Biotechnol Salt Tolerant Crops, Sch Hort, Haikou 570228, Hainan, Peoples R China
[2] Guangdong Ocean Univ, Coll Coastal Agr Sci, Natl Ctr Technol Innovat Saline Alkali Tolerant R, Zhanjiang 524088, Guangdong, Peoples R China
[3] Chinese Acad Agr Sci, Inst Cotton Res, State Key Lab Cotton Biol, Anyang 455000, Henan, Peoples R China
[4] Hainan Univ, Key Lab Germplasm Resources Biol Trop Special Orn, Minist Educ Genet & Germplasm Innovat Trop Specia, Key Lab,Sch Forestry, Haikou 570228, Hainan, Peoples R China
基金
国家重点研发计划; 海南省自然科学基金;
关键词
CBL interacting protein kinase; Drought stress; Heterologous expression; Salt stress; Dendrobium catenatum; INTERACTING PROTEIN-KINASE; CALCIUM SENSOR; TRANSCRIPTION FACTOR; STRESS RESPONSES; ABSCISIC-ACID; EXPRESSION ANALYSIS; ABIOTIC STRESS; PLANT-RESPONSE; CBL; HOMEOSTASIS;
D O I
10.1016/j.indcrop.2022.115375
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
The CBL-interacting protein kinase (CIPK) protein plays a vital role in response to abotic stresses. Dendrobium catenatum has been listed as a rare and endangered plant in China because it is difficult for it to adapt suboptimal environmental stress. However, studies on its responses to abiotic stresses are rare. Herein, the CIPK24 gene was cloned from D. catenatum. Expression pattern analysis showed that it displayed a tissue-specificity with a relatively high expression level in sepal and petal, while its expression was up-regulated by polyethylene glycol (PEG) treatment in stems and leaves, and also by salt stress in roots. Localization analysis indicated that DcCIPK24 is located to the nucleus, plasma membrane and cytoplasm. DcCIPK24 overexpression increased the tolerance of transgenic Arabidopsis to drought and salt stresses when compare with wild-type (WT) plants. Transgenic plants had lower malondialdehyde (MDA) content, while had a higher proline content and superoxide dismutase (SOD) activity than WT plants under drought or salinity stress. Furthermore, drought treatment induced faster influxes of Ca2+ and H+ in transgenic roots compared with those in WT roots. Upon treatment with NaCl, Na+ efflux of the transgenic roots was faster, but K+ efflux rate was lower compared with those of WT roots, resulting in less Na+ accumulation in transgenic plants. RNA-seq analysis showed that 114 and 497 differentially expressed genes (DEGs) were found in DcCIPK24 transgenic plants under drought and salt stress, respectively. Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses found that DEGs enriched in starch and sucrose metabolism, cutin and wax biosynthesis, and peroxisome pathway under drought stress, and enriched in phenylpropanoid biosynthesis pathway and mitogen-activated protein kinase (MAPK) signaling pathway under salt stress. These findings indicate that DcCIPK24 is a positive regulator of D. catenatum's response to drought and salt stresses, suggesting it has potential application in genetic modification of D. catenatum to enhance drought and salt tolerance.
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页数:14
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