生物物理学
膜
生物
不耐热的
胞浆
热冲击
热休克蛋白
钙
细胞生物学
膜电位
生物化学
化学
酶
基因
有机化学
作者
Younousse Saidi,Andrija Finka,Maude Muriset,Zohar Bromberg,Yoram Weiss,Frans J. M. Maathuis,Pierre Goloubinoff
出处
期刊:The Plant Cell
[Oxford University Press]
日期:2009-09-01
卷期号:21 (9): 2829-2843
被引量:280
标识
DOI:10.1105/tpc.108.065318
摘要
Land plants are prone to strong thermal variations and must therefore sense early moderate temperature increments to induce appropriate cellular defenses, such as molecular chaperones, in anticipation of upcoming noxious temperatures. To investigate how plants perceive mild changes in ambient temperature, we monitored in recombinant lines of the moss Physcomitrella patens the activation of a heat-inducible promoter, the integrity of a thermolabile enzyme, and the fluctuations of cytoplasmic calcium. Mild temperature increments, or isothermal treatments with membrane fluidizers or Hsp90 inhibitors, induced a heat shock response (HSR) that critically depended on a preceding Ca(2+) transient through the plasma membrane. Electrophysiological experiments revealed the presence of a Ca(2+)-permeable channel in the plasma membrane that is transiently activated by mild temperature increments or chemical perturbations of membrane fluidity. The amplitude of the Ca(2+) influx during the first minutes of a temperature stress modulated the intensity of the HSR, and Ca(2+) channel blockers prevented HSR and the onset of thermotolerance. Our data suggest that early sensing of mild temperature increments occurs at the plasma membrane of plant cells independently from cytosolic protein unfolding. The heat signal is translated into an effective HSR by way of a specific membrane-regulated Ca(2+) influx, leading to thermotolerance.
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