Xing T., Higgins V. J., Blumwald E.
Department of Botany, University of Toronto, 25 Willcocks Street, Toronto, Ontario M5S 3B2, Canada.
Plant Cell. 1996 Mar;8(3):555-564. doi: 10.1105/tpc.8.3.555.
The role of reversible phosphorylation of the host plasma membrane H+-ATPase in signal transduction during the incompatible interaction between tomato cells and the fungal pathogen Cladosporium fulvum was investigated. Tomato cells (with the Cf-5 resistance gene) or isolated plasma membranes from Cf-5 cells treated with elicitor preparations from race 2.3 or 4 of C. fulvum (containing the avr5 gene product) showed a marked dephosphorylation of plasma membrane H+-ATPase. Similar treatment with elicitor preparations from races 5 and 2.4.5.9.11 (lacking the avr5 gene product) showed no change in dephosphorylation. Elicitor (race 4) treatment of cells, but not of isolated plasma membranes, for 2 hr resulted in rephosphorylation of the ATPase via Ca2+-dependent protein kinases. The initial (first hour) rephosphorylation was enhanced by protein kinase C (PKC) activators and was prevented by PKC inhibitors. Activity of a second kinase appeared after 1 hr and was responsible for the continuing phosphorylation of the H+-ATPase. This latter Ca2+-dependent kinase was inhibited by a calmodulin (CaM) antagonist and by an inhibitor of Ca2+/CaM-dependent protein kinase II. The activation of the Ca2+/CaM-dependent protein kinase depended on the prior activation of the PKC-like kinase.
研究了番茄细胞与真菌病原体黄枝孢菌不亲和互作过程中,宿主质膜H⁺-ATP酶的可逆磷酸化在信号转导中的作用。用黄枝孢菌2.3、4号生理小种(含avr5基因产物)的激发子制剂处理番茄细胞(含Cf-5抗性基因)或Cf-5细胞分离的质膜,质膜H⁺-ATP酶出现明显的去磷酸化。用5号及2.4.5.9.11号生理小种(缺乏avr5基因产物)的激发子制剂进行类似处理,去磷酸化无变化。用激发子(4号生理小种)处理细胞2小时(而非分离的质膜),可使ATP酶通过Ca²⁺依赖的蛋白激酶重新磷酸化。最初(第1小时)的重新磷酸化被蛋白激酶C(PKC)激活剂增强,被PKC抑制剂阻止。1小时后出现第二种激酶的活性,它负责H⁺-ATP酶的持续磷酸化。后一种Ca²⁺依赖的激酶被钙调蛋白(CaM)拮抗剂和Ca²⁺/CaM依赖的蛋白激酶II抑制剂抑制。Ca²⁺/CaM依赖的蛋白激酶的激活依赖于类PKC激酶的预先激活。