Lee Kyounghee, Lee Hong Gil, Yoon Seongmun, Kim Hyun Uk, Seo Pil Joon
Department of Bioactive Material Sciences and Research Center of Bioactive Materials (K.L., H.G.L., P.J.S.) and Department of Chemistry and Research Institute of Physics and Chemistry (P.J.S.), Chonbuk National University, Jeonju 561-756, Republic of Korea; andDepartment of Agricultural Biotechnology, National Academy of Agricultural Science, Rural Development Administration, Jeonju 560-500, Republic of Korea (S.Y., H.U.K.).
Department of Bioactive Material Sciences and Research Center of Bioactive Materials (K.L., H.G.L., P.J.S.) and Department of Chemistry and Research Institute of Physics and Chemistry (P.J.S.), Chonbuk National University, Jeonju 561-756, Republic of Korea; andDepartment of Agricultural Biotechnology, National Academy of Agricultural Science, Rural Development Administration, Jeonju 560-500, Republic of Korea (S.Y., H.U.K.)
Plant Physiol. 2015 Jun;168(2):677-89. doi: 10.1104/pp.15.00162. Epub 2015 Apr 13.
Seed germination is a key developmental transition that initiates the plant life cycle. The timing of germination is determined by the coordinated action of two phytohormones, gibberellin and abscisic acid (ABA). In particular, ABA plays a key role in integrating environmental information and inhibiting the germination process. The utilization of embryonic lipid reserves contributes to seed germination by acting as an energy source, and ABA suppresses lipid degradation to modulate the germination process. Here, we report that the ABA-responsive R2R3-type MYB transcription factor MYB96, which is highly expressed in embryo, regulates seed germination by controlling the expression of abscisic acid-insensitive4 (ABI4) in Arabidopsis (Arabidopsis thaliana). In the presence of ABA, germination was accelerated in MYB96-deficient myb96-1 seeds, whereas the process was significantly delayed in MYB96-overexpressing activation-tagging myb96-ox seeds. Consistently, myb96-1 seeds degraded a larger extent of lipid reserves even in the presence of ABA, while reduced lipid mobilization was observed in myb96-ox seeds. MYB96 directly regulates ABI4, which acts as a repressor of lipid breakdown, to define its spatial and temporal expression. Genetic analysis further demonstrated that ABI4 is epistatic to MYB96 in the control of seed germination. Taken together, the MYB96-ABI4 module regulates lipid mobilization specifically in the embryo to ensure proper seed germination under suboptimal conditions.
种子萌发是启动植物生命周期的关键发育转变。萌发的时间由两种植物激素赤霉素和脱落酸(ABA)的协同作用决定。特别是,ABA在整合环境信息和抑制萌发过程中起关键作用。胚胎脂质储备的利用通过作为能量来源促进种子萌发,而ABA抑制脂质降解以调节萌发过程。在这里,我们报道在胚胎中高度表达的ABA响应型R2R3型MYB转录因子MYB96通过控制拟南芥中脱落酸不敏感4(ABI4)的表达来调节种子萌发。在ABA存在的情况下,MYB96缺陷型myb96-1种子的萌发加速,而在MYB96过表达的激活标签myb96-ox种子中萌发过程显著延迟。一致地,即使在ABA存在的情况下,myb96-1种子也会降解更大程度的脂质储备,而在myb96-ox种子中观察到脂质动员减少。MYB96直接调节作为脂质分解阻遏物的ABI4,以确定其时空表达。遗传分析进一步证明,在种子萌发的控制中,ABI4在MYB96之上。总之,MYB96-ABI4模块特异性地调节胚胎中的脂质动员,以确保在次优条件下种子正常萌发。