Heterologous Expression and Functional Analysis of Rice GLUTAMATE RECEPTOR-LIKE Family Indicates its Role in Glutamate Triggered Calcium Flux in Rice Roots

被引:37
作者
Ni, Jun [1 ]
Yu, Zhiming [1 ]
Du, Guankui [2 ]
Zhang, Yanyan [1 ]
Taylor, Jemma L. [3 ]
Shen, Chenjia [1 ]
Xu, Jing [1 ]
Liu, Xunyan [1 ]
Wang, Yifeng [4 ]
Wu, Yunrong [5 ]
机构
[1] Hangzhou Normal Univ, Coll Life & Environm Sci, Hangzhou 310018, Peoples R China
[2] Hainan Med Coll, Dept Biochem, Haikou 571199, Peoples R China
[3] Univ Warwick, Sch Life Sci, Gibbet Hill Campus, Coventry CV4 7AL, W Midlands, England
[4] Chinese Acad Agr Sci, China Natl Rice Res Inst, State Key Lab Rice Biol, Hangzhou 311400, Zhejiang, Peoples R China
[5] Zhejiang Univ, Coll Life Sci, State Key Lab Plant Physiol & Biochem, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Aequorin; Glu; GLR; Calcium; HEK cells; Rice; ARABIDOPSIS-THALIANA; TRANSIENT EXPRESSION; NMDA RECEPTORS; ABSCISIC-ACID; CA2+; CHANNELS; GENE; PLANTS; DESENSITIZATION; INVOLVEMENT;
D O I
10.1186/s12284-016-0081-x
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Background: Tremendous progress has been made in understanding the functions of the GLUTAMATE RECEPTOR-LIKE (GLR) family in Arabidopsis. Still, the functions of OsGLRs in rice, especially the ion channel activities, are largely unknown. Results: Using the aequorin-based luminescence imaging system, we screened the specificity of amino acids involved in the induction of Ca2+ flux in rice roots. Of all the amino acids tested, glutamate (Glu) was the only one to trigger Ca2+ flux significantly in rice roots. Detailed analysis showed a dose response of Ca2+ increase to different concentrations of Glu. In addition, the Ca2+ spike response to Glu was rapid, within 20 s after the application. A desensitization assay and pharmacological tests showed that the Glu-triggered Ca2+ flux is mediated by OsGLRs. Whole genome analysis identified 13 OsGLR genes in rice, and these genes have various expression patterns in different tissues. Subcellular localization studies showed that all the OsGLRs examined are likely localized to the plasma membrane. Bacteria growth assays showed that at least OsGLR2.1 and OsGLR3.2 have the potential to mediate ion uptake in bacteria. Further analysis using Fura-2-based Ca2+ imaging revealed a Glu-triggered Ca2+ increase in OsGLR2.1-expressing human embryonic kidney (HEK) cells. Conclusions: Our work provides a molecular basis for investigating mechanisms of Glu-triggered Ca2+ flux in rice.
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页数:14
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