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Calcium is involved in nitric oxide- and auxin-induced lateral root formation in rice

机译:钙参与一氧化氮和植物生长素诱导的水稻侧根形成

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In the present study, the role of nitric oxide (NO) in the regulation of lateral root (LR) formation in rice was examined. Application of sodium nitroprusside (SNP; a NO donor) and indole-3-butyric acid (IBA; a naturally occurring auxin) to rice seedlings induced LR formation. The effect is specific for NO because the NO scavenger 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3- oxide (cPTIO) blocked the action of SNP and IBA. Endogenous NO was detected by the specific fluorescence probe 4-amino-5-methylamino-2′,7′-difluorofluorescein diacetate. SNP- and IBA-induced NO fluorescence was specifically suppressed by cPTIO. Nitrate reductase (NR) inhibitor sodium tungstate completely inhibited IBA-induced LR formation and NO fluorescence. However, nitric oxide synthase inhibitor N ~G-nitro-l-arginine methyl ester hydrochloride slightly reduced IBA-induced LR formation and NO generation. It appears that NO generation that occurs in response to IBA might primarily involve NR activity. Moreover, NO production caused by SNP and IBA was localized in root area corresponding to LR emergence. The effects of Ca ~(2+) chelators, Ca ~(2+)-channel inhibitors, and calmodulin antagonists on LR formation induced by SNP and IBA were also examined. All these inhibitors were effective in reducing the action of SNP and IBA. However, Ca ~(2+) chelators and Ca ~(2+)-channel inhibitors had no effect on SNP- and IBA-induced NO generation. It is concluded that cytosolic levels of Ca ~(2+) may regulate SNP and IBA action through calmodulin-dependent mechanism.
机译:在本研究中,研究了一氧化氮(NO)在调节水稻侧根(LR)形成中的作用。将硝普钠(SNP; NO供体)和吲哚-3-丁酸(IBA;天然生长素)应用于水稻幼苗可诱导LR形成。由于NO清除剂2-(4-羧苯基)-4,4,5,5-四甲基咪唑啉-1-氧基1-3氧化物(cPTIO)阻止了SNP和IBA的作用,因此该效果对NO特定。通过特异性荧光探针4-氨基-5-甲基氨基-2',7'-二氟荧光素二乙酸酯检测到内源性NO。 cPTIO特异性抑制了SNP和IBA诱导的NO荧光。硝酸还原酶(NR)抑制剂钨酸钠完全抑制IBA诱导的LR形成和NO荧光。然而,一氧化氮合酶抑制剂N〜G-硝基-1-精氨酸甲酯盐酸盐可稍微减少IBA诱导的LR的形成和NO的产生。似乎响应IBA而发生的NO生成可能主要涉及NR活性。此外,由SNP和IBA引起的NO生成位于与LR出现相对应的根区域。还研究了Ca〜(2+)螯合剂,Ca〜(2 +)-通道抑制剂和钙调蛋白拮抗剂对SNP和IBA诱导的LR形成的影响。所有这些抑制剂均有效降低SNP和IBA的作用。但是,Ca〜(2+)螯合剂和Ca〜(2+)通道抑制剂对SNP和IBA诱导的NO生成没有影响。结论:Ca〜(2+)的胞质水平可能通过钙调蛋白依赖性机制调节SNP和IBA的作用。

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