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The Induction of Seed Germination in Arabidopsis thaliana Is Regulated Principally by Phytochrome B and Secondarily by Phytochrome A.

机译:拟南芥种子萌发的诱导主要受植物色素B的调节其次受植物色素A的调节。

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摘要

We examined whether spectrally active phytochrome A (PhyA) and phytochrome B (PhyB) play specific roles in the induction of seed germination in Arabidopsis thaliana (L.) Heynh., using PhyA- and PhyB-null mutants, fre1-1 (A. Nagatani, J.W. Reed, J. Chory [1993] Plant Physiol 102: 269-277) and hy3-Bo64 (J. Reed, P.Nagpal, D.S. Poole, M. Furuya, J. Chory [1993] Plant Cell 5: 147-157). When dormant seeds of each genotype imbibed in the dark on aqueous agar plates, the hy3 (phyB) mutant did not germinate, whereas the fre1 (phyA) mutant germinated at a rate of 50 to 60%, and the wild type (WT) germinated at a rate of 60 to 70%. By contrast, seeds of all genotypes germinated to nearly 100% when plated in continuous irradiation with white or red light. When plated in continuous far-red light, however, frequencies of seed germination of the WT and the fre1 and hy3 mutants averaged 14, nearly 0, and 47%, respectively, suggesting that PhyB in the red-absorbing form prevents PhyA-dependent germination under continuous far-red light. When irradiated briefly with red or far-red light after imbibition for 1 h, a typical photoreversible effect on seed germination was observed in the fre1 mutant and the WT but not in the hy3 mutant. In contrast, when allowed to imbibe in the dark for 24 to 48 h and exposed to red light, the seed germination frequencies of the hy3 mutant were more than 40%. Immunoblot analyses of the mutant seeds showed that PhyB apoprotein accumulated in dormant seeds of the WT and the fre1 mutant as much as in the seeds that had imbibed. In contrast, PhyA apoprotein, although detected in etiolated seedlings grown in the dark for 5 d, was not detectable in the dormant seeds of the WT and the hy3 mutant. The above physiological and immunochemical evidence indicates that PhyB in the far-red-absorbing form was stored in the Arabidopsis seeds and resulted in germination in the dark. Hence, PhyA does not play any role in dark germination but induces germination under continuous irradiation with far-red light. Finally, we examined seeds from a signal transduction mutant, det1, and a det1/hy3 double mutant. The det1 seeds exhibited photoreversible responses of germination on aqueous agar plates, and the det1/hy3 double mutant seeds did not. Hence, DET1 is likely to act in a distinct pathway from PhyB in the photoregulation of seed germination.
机译:我们使用PhyA-和PhyB-null突变体fre1-1(A.A.)检查了具有光谱活性的植物色素A(PhyA)和植物色素B(PhyB)在拟南芥(L.)Heynh。的种子萌发诱导中是否起特定作用。 Nagatani,JW Reed,J. Chory [1993]植物生理学102:269-277)和hy3-Bo64(J. Reed,P.Nagpal,DS Poole,M.Furuya,J.Cory [1993]植物细胞5:147 -157)。当每种基因型的休眠种子在黑暗中浸入水性琼脂平板上时,hy3(phyB)突变体不会发芽,而fre1(phyA)突变体则以50%至60%的速率发芽,而野生型(WT)则发芽以60%到70%的比率。相反,在连续照射白光或红光的情况下,所有基因型的种子发芽率接近100%。但是,当在连续的远红光条件下接种时,野生型以及fre1和hy3突变体的种子发芽频率分别平均为14,接近0和47%,这表明呈红色吸收形式的PhyB阻止了依赖PhyA的发芽。在连续的远红光下。吸光后用红色或远红外光短暂照射1 h,在fre1突变体和WT中观察到对种子萌发的典型光可逆效应,但在hy3突变体中未观察到。相反,当允许其在黑暗中吸收24至48小时并暴露于红光下时,hy3突变体的种子发芽频率超过40%。突变体种子的免疫印迹分析表明,PhyB载脂蛋白在野生型和fre1突变体的休眠种子中积累的数量与已吸收的种子一样多。相反,尽管在黑暗中生长5 d的黄化幼苗中检测到PhyA载脂蛋白,但在WT和hy3突变体的休眠种子中未检测到。上述生理和免疫化学证据表明,远红吸收形式的PhyB被储存在拟南芥种子中,并在黑暗中发芽。因此,PhyA在暗发芽中不发挥任何作用,但是在连续的远红光照射下诱导发芽。最后,我们检查了信号转导突变体det1和det1 / hy3双突变体的种子。 det1种子在水性琼脂平板上显示出光可逆的萌发反应,而det1 / hy3双重突变种子则没有。因此,DET1可能在种子萌发的光调节中以与PhyB不同的途径起作用。

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