Effects of 1,2,4-Trichlorobenzene and Mercury Ion Stress on Ca^2+ Fluxion and Protein Phosphorylation in Rice  被引量:3

Effects of 1,2,4-Trichlorobenzene and Mercury Ion Stress on Ca^(2+) Fluxion and Protein Phosphorylation in Rice

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作  者:GE Cai-lin WANG Ze-gang WAN Ding-zhen DING Yan WANG Yu-long SHANG Qi LUO Shi-shi MA Fei 

机构地区:[1]Jiangsu Provincial Key Laboratory of Crop Genetics and Physiology, Yangzhou University, Yangzhou 225009, China

出  处:《Rice science》2007年第4期272-282,共11页水稻科学(英文版)

基  金:supported by the National Natural Science Foundation of China(Grant No.30300026).

摘  要:The effects of 5 mg/L 1,2,4-trichlorobenzene (TCB) and 0.1 mmol/L mercury ion (Hg^2+) stresses on Ca^2+ fluxion and protein phosphorylation in rice seedlings were investigated by isotope exchange kinetics and in vitro phosphorylation assay. The Ca^2+ absorption in rice leaves and Ca^2+ transportation from roots to leaves were promoted significantly in response to Hg^2+ and TCB treatments for 4-48 h. The Ca^2+ absorption peaks presented in the leaves when the rice seedlings were exposed to Hg^2+ for 8-12 h or to TCB for 12-24 h. Several Ca^2+ absorption peaks presented in the roots during rice seedlings being exposed to Hg^2+ and TCB, and the first Ca^2+ absorption peak was at 8 h after being exposed to Hg^2+ and TCB The result of isotope exchange kinetic analysis confirmed that short-term (8 h) Hg^2+ and TCB stresses caused Ca^2+ channels or pumps located on plasmalemma to open transiently. The phosphorylation assay showed that short-term TCB stress enhanced protein phosphorylation in rice roots (TCB treatment for 4-8 h) and leaves (TCB treatment for 4-24 h), and short-term (4-8 h) Hg^2+ stress also enhanced protein phosphorylation in rice leaves. The enhancement of protein phosphorylation in both roots and leaves corresponded with the first Ca^2+ absorption peak, which confirmed that the enhancement of protein phosphorylation caused by TCB or Hg^2+ stress might be partly triggered by the increases of cytosolic calcium. TCB treatment over 12 h inhibited protein phosphorylation in rice roots, which might be partly due to that TCB stress suppressed the protein kinase activity. Whereas, Hg^2+ treatment inhibited protein phosphorylation in rice roots, and Hg^2+ treatment over 12 h inhibited protein phosphorylation in rice leaves. This might be attributed to that not only the protein kinase activity, but also the expressions of phosphorylation proteins were restrained by Hg^2+ stress.The effects of 5 mg/L 1,2,4-trichlorobenzene (TCB) and 0.1 mmol/L mercury ion (Hg^2+) stresses on Ca^2+ fluxion and protein phosphorylation in rice seedlings were investigated by isotope exchange kinetics and in vitro phosphorylation assay. The Ca^2+ absorption in rice leaves and Ca^2+ transportation from roots to leaves were promoted significantly in response to Hg^2+ and TCB treatments for 4-48 h. The Ca^2+ absorption peaks presented in the leaves when the rice seedlings were exposed to Hg^2+ for 8-12 h or to TCB for 12-24 h. Several Ca^2+ absorption peaks presented in the roots during rice seedlings being exposed to Hg^2+ and TCB, and the first Ca^2+ absorption peak was at 8 h after being exposed to Hg^2+ and TCB The result of isotope exchange kinetic analysis confirmed that short-term (8 h) Hg^2+ and TCB stresses caused Ca^2+ channels or pumps located on plasmalemma to open transiently. The phosphorylation assay showed that short-term TCB stress enhanced protein phosphorylation in rice roots (TCB treatment for 4-8 h) and leaves (TCB treatment for 4-24 h), and short-term (4-8 h) Hg^2+ stress also enhanced protein phosphorylation in rice leaves. The enhancement of protein phosphorylation in both roots and leaves corresponded with the first Ca^2+ absorption peak, which confirmed that the enhancement of protein phosphorylation caused by TCB or Hg^2+ stress might be partly triggered by the increases of cytosolic calcium. TCB treatment over 12 h inhibited protein phosphorylation in rice roots, which might be partly due to that TCB stress suppressed the protein kinase activity. Whereas, Hg^2+ treatment inhibited protein phosphorylation in rice roots, and Hg^2+ treatment over 12 h inhibited protein phosphorylation in rice leaves. This might be attributed to that not only the protein kinase activity, but also the expressions of phosphorylation proteins were restrained by Hg^2+ stress.

关 键 词:RICE mercury ion 1 2 4-TRICHLOROBENZENE calcium ion fluxion protein phosphorylation 

分 类 号:S511[农业科学—作物学]

 

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