The Arabidopsis Prohibitin Gene PHB3 Functions in Nitric Oxide-Mediated Responses and in Hydrogen Peroxide-Induced Nitric Oxide Accumulation

被引:95
|
作者
Wang, Yong [1 ]
Ries, Amber [1 ]
Wu, Kati [1 ]
Yang, Albert [1 ]
Crawford, Nigel M. [1 ]
机构
[1] Univ Calif San Diego, Sect Cell & Dev Biol, Div Biol Sci, La Jolla, CA 92093 USA
来源
PLANT CELL | 2010年 / 22卷 / 01期
基金
美国国家卫生研究院;
关键词
INDUCED STOMATAL CLOSURE; NITRATE REDUCTASE; CROSS-TALK; DISEASE RESISTANCE; PLANT DEVELOPMENT; STRESS RESPONSES; IN-VIVO; SIGNAL; NO; EXPRESSION;
D O I
10.1105/tpc.109.072066
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To discover genes involved in nitric oxide (NO) metabolism, a genetic screen was employed to identify mutants defective in NO accumulation after treatment with the physiological inducer hydrogen peroxide. In wild-type Arabidopsis thaliana plants, NO levels increase eightfold in roots after H2O2 treatment for 30 min. A mutant defective in H2O2-induced NO accumulation was identified, and the corresponding mutation was mapped to the prohibitin gene PHB3, converting the highly conserved Gly-37 to an Asp in the protein's SPFH domain. This point mutant and a T-DNA insertion mutant were examined for other NO-related phenotypes. Both mutants were defective in abscisic acid-induced NO accumulation and stomatal closure and in auxin-induced lateral root formation. Both mutants were less sensitive to salt stress, showing no increase in NO accumulation and less inhibition of primary root growth in response to NaCl treatment. In addition, light-induced NO accumulation was dramatically reduced in cotyledons. We found no evidence for impaired H2O2 metabolism or signaling in the mutants as H2O2 levels and H2O2-induced gene expression were unaffected by the mutations. These findings identify a component of the NO homeostasis system in plants and expand the function of prohibitin genes to include regulation of NO accumulation and NO-mediated responses.
引用
收藏
页码:249 / 259
页数:11
相关论文
共 50 条
  • [21] Peroxide-induced iron signaling and apoptosis: The effect of nitric oxide.
    Kalyanaraman, B
    CHEMICAL RESEARCH IN TOXICOLOGY, 2003, 16 (12) : 1664 - 1665
  • [22] The effect of sildenafil citrate on nitric oxide-mediated vascular responses.
    Dishy, V
    Sofowora, G
    Kandcer, M
    Zhan, F
    Wood, AJJ
    Stein, CM
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2000, 67 (02) : 141 - 141
  • [23] Salt Stress Reduces Root Meristem Size by Nitric Oxide-Mediated Modulation of Auxin Accumulation and Signaling in Arabidopsis
    Liu, Wen
    Li, Rong-Jun
    Han, Tong-Tong
    Cai, Wei
    Fu, Zheng-Wei
    Lu, Ying-Tang
    PLANT PHYSIOLOGY, 2015, 168 (01) : 343 - U607
  • [24] Inhibition of root meristem growth by cadmium involves nitric oxide-mediated repression of auxin accumulation and signalling in Arabidopsis
    Yuan, Hong-Mei
    Huang, Xi
    PLANT CELL AND ENVIRONMENT, 2016, 39 (01): : 120 - 135
  • [26] Synthetic wogonin derivatives suppress lipopolysaccharide-induced nitric oxide production and hydrogen peroxide-induced cytotoxicity
    Chun, W
    Lee, HJ
    Kong, PJ
    Lee, GH
    Cheong, IY
    Park, H
    Kim, SS
    ARCHIVES OF PHARMACAL RESEARCH, 2005, 28 (02) : 216 - 219
  • [27] Nitric oxide production decreases after salt loading but is not related to blood pressure changes or nitric oxide-mediated vascular responses
    Dishy, V
    Sofowora, GG
    Imamura, H
    Nishimi, Y
    Xie, HG
    Wood, AJJ
    Stein, CM
    JOURNAL OF HYPERTENSION, 2003, 21 (01) : 153 - 157
  • [28] Nitric oxide-mediated vasorelaxation induced by sodium polyoxyethylene laurylether sulfate
    Koyama, K
    Kasuya, Y
    Koyama, K
    Goto, K
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 1997, 145 (02) : 294 - 300
  • [29] Synthetic wogonin derivatives suppress lipopolysaccharide-induced nitric oxide production and hydrogen peroxide-induced cytotoxicity
    Wanjoo Chun
    Hee Jae Lee
    Pil-Jae Kong
    Gun Hee Lee
    ll-Young Cheongsu
    Haeil Park
    Sung-Soo Kim
    Archives of Pharmacal Research, 2005, 28 : 216 - 219
  • [30] Nitric oxide protects Cu,Zn-superoxide dismutase from hydrogen peroxide-induced inactivation
    Kim, YS
    Han, SW
    FEBS LETTERS, 2000, 479 (1-2) : 25 - 28