Role of OsCZMT1 in Na+ and Mg2+ transport and salinity insensitivity

被引:4
|
作者
Lim, Sung Don [1 ,2 ]
Kim, Jong Ho [3 ]
Lee, Jeongeun [3 ]
Hwang, Sun-Goo [4 ]
Shim, Su-Hyeon [5 ]
Jeon, Jong-Seong [5 ]
Jang, Cheol Seong [1 ,3 ]
机构
[1] Kangwon Natl Univ, Agr & Life Sci Res Inst, Chunchon 24341, South Korea
[2] Sangji Univ, Dept Plant Life & Resource Sci, Mol Plant Physiol Lab, Wonju 26339, South Korea
[3] Kangwon Natl Univ, Interdisciplinary Program Smart Agr, Plant Genom Lab, Chunchon 24341, South Korea
[4] Sangji Univ, Dept Plant Life & Resource Sci, Plant Bioconvergence Lab, Wonju 26339, South Korea
[5] Kyung Hee Univ, Grad Sch Biotechnol & Crop Biotech Inst, Yongin 17104, South Korea
基金
新加坡国家研究基金会;
关键词
CorA-like ZntB cation transporter; Mg2+ transporter; Na+ transporter; Rice (Oryza sativa); Salinity stress tolerance; Gamma-ray mutant; SALT TOLERANCE; MAGNESIUM TRANSPORT; STRESS TOLERANCE; HKT TRANSPORTER; READ ALIGNMENT; RICE OSHKT2/1; EXPRESSION; GENE; ARABIDOPSIS; SODIUM;
D O I
10.1016/j.envexpbot.2021.104754
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Salinity stress is one of the most important abiotic stress factors affecting rice production worldwide. Using a forward genetics approach, a salt-insensitive TILLING line 1 (sitl1) rice mutant was isolated from a TILLING population. The sitl1 mutant exhibited reduced root growth and leaf chlorophyll content when grown under normal conditions, owing to a reduced ability to take up Mg2+; however, the defective phenotype could be restored by Mg2+ supplementation. Ionomic analysis revealed that the salinity insensitivity of sitl1 was the result of significantly reduced Mg2+ and Na+, and whole genome and RNA sequencing revealed that the sitl1 mutant caused a frameshift in the OsCZMT1 protein's CorA-like ZntB cation transfer domain. Transient expression of an OsCZMT1-sGFP fusion protein revealed that OsCZMT1 was localized to the plasma membrane, and comprehensive expression analysis revealed that OsCZMT1 was mainly expressed in the roots and leaves of seedlings and highly upregulated in response to salinity stress. Complementation assays in yeast and CRISPR/Cas9-mediated knock-out mutants reveal that OsCZMT1 possesses both Mg2+ and Na+ transport activity. Taken together, these findings suggest that the identified OsCZMT1 frameshift mutation is responsible for the reduced Na+ and Mg2+ transport abilities, and that those reduced transport abilities confer salinity insensitivity.
引用
收藏
页数:17
相关论文
共 50 条
  • [21] THE ROLE OF MG2+ AND K+ IN THE PHOSPHORYLATION OF NA+,K+-ATPASE BY ATP IN THE PRESENCE OF DIMETHYLSULFOXIDE BUT IN THE ABSENCE OF NA+
    FONTES, CFL
    BARRABIN, H
    SCOFANO, HM
    NORBY, JG
    BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1104 (01) : 215 - 225
  • [22] Regulation of Na+/Mg2+ Exchange in Sickle Erythrocytes By Endothelin-1
    Rivera, Pablo A.
    Inostroza, Yaritza
    Romero, Jose R.
    Rivera, Alicia
    BLOOD, 2014, 124 (21)
  • [23] Na+/Mg2+ transporter acts as a Mg2+ buffering mechanism in PC12 cells
    Kubota, T
    Tokuno, K
    Nakagawa, J
    Kitamura, Y
    Ogawa, H
    Suzuki, Y
    Suzuki, K
    Oka, K
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 303 (01) : 332 - 336
  • [24] NA+/K+-ATPASE - MODES OF INHIBITION BY MG2+
    ROBINSON, JD
    PRATAP, PR
    BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1061 (02) : 267 - 278
  • [25] Characterization of Na+/Mg2+ exchange in sickle erythrocytes.
    Rivera, A
    Ferreira, AM
    Romero, JR
    Brugnara, C
    BLOOD, 2001, 98 (11) : 485A - 485A
  • [26] RNA helix stability in mixed Na+/Mg2+ solution
    Tan, Zhi-Jie
    Chen, Shi-Jie
    BIOPHYSICAL JOURNAL, 2007, 92 (10) : 3615 - 3632
  • [27] Mechanism of Mg2+ Binding in the Na+,K+-ATPase
    Pilotelle-Bunner, Anne
    Cornelius, Flemming
    Sebban, Pierre
    Kuchel, Philip W.
    Clarke, Ronald J.
    BIOPHYSICAL JOURNAL, 2009, 96 (09) : 3753 - 3761
  • [28] Insulin regulates human erythrocyte Na+/Mg2+ exchange
    Ferreira, A
    Romero, JR
    Rivera, A
    JOURNAL OF HYPERTENSION, 2002, 20 : S279 - S279
  • [29] Na+/Mg2+ exchange is functionally coupled to the insulin receptor
    Ferreira, A
    Rivera, A
    Romero, JR
    JOURNAL OF CELLULAR PHYSIOLOGY, 2004, 199 (03) : 434 - 440
  • [30] Reversibility of Na+/Mg2+ antiport in HL 60 cells
    Günther, T
    Förster, RM
    MAGNESIUM-BULLETIN, 2000, 22 (01): : 10 - 14