Bjornson Marta, Benn Geoffrey, Song Xingshun, Comai Luca, Franz Annaliese K, Dandekar Abhaya M, Drakakaki Georgia, Dehesh Katayoon
Department of Plant Biology (M.B., G.B., L.C., K.D.), Department of Plant Sciences (M.B., A.M.D., G.D.), and Department of Chemistry (A.K.F.), University of California, Davis, California 95616; andCollege of Life Science, Northeast Forestry University, Harbin 150040, People's Republic of China (X.S.).
Department of Plant Biology (M.B., G.B., L.C., K.D.), Department of Plant Sciences (M.B., A.M.D., G.D.), and Department of Chemistry (A.K.F.), University of California, Davis, California 95616; andCollege of Life Science, Northeast Forestry University, Harbin 150040, People's Republic of China (X.S.)
Plant Physiol. 2014 Oct;166(2):988-96. doi: 10.1104/pp.114.245944. Epub 2014 Aug 25.
To survive environmental challenges, plants have evolved tightly regulated response networks, including a rapid and transient general stress response (GSR), followed by well-studied stress-specific responses. The mechanisms underpinning the GSR have remained elusive, but a functional cis-element, the rapid stress response element (RSRE), is known to confer transcription of GSR genes rapidly (5 min) and transiently (peaking 90-120 min after stress) in vivo. To investigate signal transduction events in the GSR, we used a 4xRSRE:LUCIFERASE reporter in Arabidopsis (Arabidopsis thaliana), employing complementary approaches of forward and chemical genetic screens, and identified components regulating peak time versus amplitude of RSRE activity. Specifically, we identified a mutant in CALMODULIN-BINDING TRANSCRIPTIONAL ACTIVATOR3 (CAMTA3) with reduced RSRE activation, verifying this transcription factor's role in activation of the RSRE-mediated GSR. Furthermore, we isolated a mutant in MITOGEN-ACTIVATED PROTEIN KINASE (MAPK) KINASE KINASE1 (mekk1-5), which displays increased basal and an approximately 60-min earlier peak of wound-induced RSRE activation. The double mekk1/camta3 mutant positioned CAMTA3 downstream of MEKK1 and verified their distinct roles in GSR regulation. mekk1-5 displays programmed cell death and overaccumulates reactive oxygen species and salicylic acid, hallmarks of the hypersensitive response, suggesting that the hypersensitive response may play a role in the RSRE phenotype in this mutant. In addition, chemical inhibition studies suggest that the MAPK network is required for the rapid peak of the RSRE response, distinguishing the impact of chronic (mekk1-5) from transient (chemical inhibition) loss of MAPK signaling. Collectively, these results reveal underlying regulatory components of the plant GSR and further define their distinct roles in the regulation of this key biological process.
为了在环境挑战中生存,植物进化出了调控严格的反应网络,包括快速且短暂的一般胁迫反应(GSR),随后是经过充分研究的胁迫特异性反应。支撑GSR的机制一直难以捉摸,但一种功能性顺式元件,即快速胁迫反应元件(RSRE),已知可在体内快速(5分钟)且短暂地(胁迫后90 - 120分钟达到峰值)赋予GSR基因转录。为了研究GSR中的信号转导事件,我们在拟南芥(Arabidopsis thaliana)中使用了一个4xRSRE:荧光素酶报告基因,采用正向和化学遗传筛选的互补方法,并鉴定了调节RSRE活性峰值时间与幅度的成分。具体而言,我们鉴定出一个钙调蛋白结合转录激活因子3(CAMTA3)突变体,其RSRE激活降低,证实了该转录因子在激活RSRE介导的GSR中的作用。此外,我们分离出一个丝裂原活化蛋白激酶(MAPK)激酶激酶1(mekk1 - 5)突变体,它表现出基础活性增加以及伤口诱导的RSRE激活峰值提前约60分钟。mekk1/camta3双突变体将CAMTA3定位在MEKK1下游,并证实了它们在GSR调控中的不同作用。mekk1 - 5表现出程序性细胞死亡,并且活性氧和水杨酸过度积累,这是过敏反应的特征,表明过敏反应可能在该突变体的RSRE表型中起作用。此外,化学抑制研究表明,MAPK网络是RSRE反应快速峰值所必需的,这区分了慢性(mekk1 - 5)与短暂(化学抑制)MAPK信号缺失的影响。总的来说,这些结果揭示了植物GSR的潜在调控成分,并进一步明确了它们在这一关键生物学过程调控中的不同作用。