Department of Plant Systems Biology, Center for Life and Food Sciences, Technische Universtität München, Emil-Ramann-Strasse 4, 85354 Freising, Germany.
Development. 2012 Nov;139(21):4020-8. doi: 10.1242/dev.081240. Epub 2012 Sep 19.
When penetrating the soil during germination, dicotyledonous plants protect their shoot apical meristem through the formation of an apical hook. Apical hook formation is a dynamic process that can be subdivided into hook formation, maintenance and opening. It has previously been established that these processes require the transport and signaling of the phytohormone auxin, as well as the biosynthesis and signaling of the phytohormones ethylene and gibberellin (GA). Here, we identify a molecular mechanism for an auxin-GA crosstalk by demonstrating that the auxin transport-regulatory protein kinase WAG2 is a crucial transcription target during apical hook opening downstream from GA signaling. We further show that WAG2 is directly activated by PHYTOCHROME INTERACTING FACTOR 5 (PIF5), a light-labile interactor of the DELLA repressors of the GA pathway. We find that wag2 mutants are impaired in the repression of apical hook opening in dark-grown seedlings and that this phenotype correlates with GA-regulated WAG2 expression in the concave (inner) side of the apical hook. Furthermore, wag2 mutants are also impaired in the maintenance or formation of a local auxin maximum at the site of WAG2 expression in the hook. WAG2 is a regulator of PIN auxin efflux facilitators and, in line with previous data, we show that this kinase can phosphorylate the central intracellular loop of all PIN-FORMED (PIN) proteins regulating apical hook opening. We therefore propose that apical hook opening is controlled by the differential GA-regulated accumulation of WAG2 and subsequent local changes in PIN-mediated auxin transport.
在发芽过程中穿透土壤时,双子叶植物通过形成顶端弯钩来保护其茎尖分生组织。顶端弯钩的形成是一个动态过程,可以细分为弯钩的形成、维持和打开。先前已经确立,这些过程需要植物激素生长素的运输和信号转导,以及植物激素乙烯和赤霉素(GA)的生物合成和信号转导。在这里,我们通过证明生长素运输调节蛋白激酶 WAG2 是 GA 信号下游顶端弯钩打开过程中的关键转录靶标,确定了生长素-GA 串扰的分子机制。我们进一步表明,WAG2 被光不稳定的赤霉素途径 DELLA 抑制剂 PHYTOCHROME INTERACTING FACTOR 5(PIF5)直接激活。我们发现 wag2 突变体在黑暗中生长的幼苗中顶端弯钩打开的抑制作用受损,并且该表型与 GA 调节的 WAG2 在顶端弯钩凹面(内部)的表达相关。此外,wag2 突变体在 WAG2 在钩中的表达部位处局部生长素最大值的维持或形成中也受到损害。WAG2 是 PIN 生长素外排促进因子的调节剂,与先前的数据一致,我们表明这种激酶可以磷酸化调节顶端弯钩打开的所有 PIN-FORMED(PIN)蛋白的中央细胞内环。因此,我们提出顶端弯钩的打开受 GA 调节的 WAG2 的差异积累以及随后局部变化的 PIN 介导的生长素运输控制。