Ueguchi-Tanaka M, Fujisawa Y, Kobayashi M, Ashikari M, Iwasaki Y, Kitano H, Matsuoka M
Bioscience Center and Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya, 464-8601, Japan.
Proc Natl Acad Sci U S A. 2000 Oct 10;97(21):11638-43. doi: 10.1073/pnas.97.21.11638.
Previously, we reported that the rice dwarf mutant, d1, is defective in the alpha subunit of the heterotrimeric G protein (Galpha). In the present study, gibberellin (GA) signaling in d1 and the role of the Galpha protein in the GA-signaling pathway were investigated. Compared with the wild type, GA induction of alpha-amylase activity in aleurone cells of d1 was greatly reduced. Relative to the wild type, the GA(3)-treated aleurone layer of d1 had lower expression of Ramy1A, which encodes alpha-amylase, and OsGAMYB, which encodes a GA-inducible transcriptional factor, and no increase in expression of Ca(2 +)-ATPase. However, in the presence of high GA concentrations, alpha-amylase induction occurred even in d1. The GA sensitivity of second leaf sheath elongation in d1 was similar to that of the wild type in terms of dose responsiveness, but the response of internode elongation to GA was much lower in d1. Furthermore, Os20ox expression was up-regulated, and the GA content was elevated in the stunted internodes of d1. All these results suggest that d1 affects a part of the GA-signaling pathway, namely the induction of alpha-amylase in the aleurone layer and internode elongation. In addition, a double mutant between d1 and another GA-signaling mutant, slr, revealed that SLR is epistatic to the D1, supporting that the Galpha protein is involved in GA signaling. However, the data also provide evidence for the presence of an alternative GA-signaling pathway that does not involve the Galpha protein. It is proposed that GA signaling via the Galpha protein may be more sensitive than that of the alternative pathway, as indicated by the low GA responsiveness of this Galpha-independent pathway.
此前,我们报道过水稻矮化突变体d1在异源三聚体G蛋白(Gα)的α亚基上存在缺陷。在本研究中,我们对d1中的赤霉素(GA)信号传导以及Gα蛋白在GA信号通路中的作用进行了研究。与野生型相比,d1糊粉层细胞中GA诱导的α-淀粉酶活性大幅降低。相对于野生型,经GA(3)处理的d1糊粉层中,编码α-淀粉酶的Ramy1A和编码GA诱导型转录因子的OsGAMYB的表达较低,且Ca(2 +)-ATPase的表达没有增加。然而,在高浓度GA存在的情况下,即使是d1也会发生α-淀粉酶诱导。就剂量反应性而言,d1第二叶鞘伸长的GA敏感性与野生型相似,但d1节间伸长对GA的反应要低得多。此外,Os20ox表达上调,d1发育不良的节间中GA含量升高。所有这些结果表明,d1影响GA信号通路的一部分,即糊粉层中α-淀粉酶的诱导和节间伸长。此外,d1与另一个GA信号突变体slr之间的双突变体表明,SLR对D1具有上位性,支持Gα蛋白参与GA信号传导。然而,这些数据也为存在不涉及Gα蛋白的替代GA信号通路提供了证据。据推测,通过Gα蛋白的GA信号传导可能比替代途径更敏感,如这条不依赖Gα的途径对GA的低反应性所示。