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作 者:于荣[1] 孙丽[1] 李学东[1] 王学臣[2] 袁明[2] 吴忠义[3]
机构地区:[1]首都师范大学生命科学学院,北京100037 [2]中国农业大学生物学院植物生理生化国家重点实验室,北京100094 [3]北京市农林科学院北京农业生物技术研究中心,北京100090
出 处:《分子细胞生物学报》2007年第3期258-262,共5页Journal of Molecular Cell Biology
基 金:北京市科委科技新星项目(2003B34);国家自然基金项目(30600318;30400228)
摘 要:植物细胞微管骨架的不同排列方式对细胞的生长分化及形态建成具有重要意义,微管的这种动态组织行为不仅需要自身的组成蛋白-微管蛋白(tubulin),还要有微管辅助蛋白MAPs(Microtubule—associated proteins)的参与。即MAPs是一类能够与微管骨架特异结合并调节其动态装配过程及其结构.A tMAP65-1 gene was cloned from Arabidopsis genome. A plant expression vector containing AtMAP65-1-GFP fusion gene driven by 35S promoter was constructed and introduced into Arabidopsis by Agrobacterium infection. Under confocal laser scanning microscope (CLSM), it was found that in the light-induced opening guard cells AtMAP65-1 was distributed radiately from dorsal wall to ventral wall in a bundling way. Treated with microtubule specific inhibitor-Vinblastine (10μmol/L) for 90 min,the organization of AtMAP65-1 in guard cell was disrupted dramatically. Following the depolymerization of cortical microtubule and the decreasing of stomatal aperture,the fluorescence of AtMAP65-1 became to be fragmented into dotted spots. The organization of AtMAP65-1 was broken up completely when the treatment was up to 120 min. In the dark-induced closing guard cells, AtMAP65-1 was turned into fragments and was randomly dispersed throughout the cells. That is, AtMAP65-1 is co-localized with cortical microtubules. The results suggest that AtMAP65-1 binds cortical microtubules, and it may regulate the arrangement of cortical microtubules, which helps us gain more insights into the role of AtMAP65-1 in stomatal move- ment.
关 键 词:气孔运动 周质微管 微管结合蛋白AtMAP65-1 长春花碱
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