Kim Hyo Jung, Hong Sung Hyun, Kim You Wang, Lee Il Hwan, Jun Ji Hyung, Phee Bong-Kwan, Rupak Timilsina, Jeong Hana, Lee Yeonmi, Hong Byoung Seok, Nam Hong Gil, Woo Hye Ryun, Lim Pyung Ok
Center for Plant Aging Research, Institute for Basic Science (IBS), Daegu 711-873, Republic of Korea.
Department of New Biology, Daegu Gyeongbuk Institute of Science & Technology (DGIST), Daegu 711-873, Republic of Korea.
J Exp Bot. 2014 Jul;65(14):4023-36. doi: 10.1093/jxb/eru112. Epub 2014 Mar 22.
Leaf senescence is a finely tuned and genetically programmed degeneration process, which is critical to maximize plant fitness by remobilizing nutrients from senescing leaves to newly developing organs. Leaf senescence is a complex process that is driven by extensive reprogramming of global gene expression in a highly coordinated manner. Understanding how gene regulatory networks involved in controlling leaf senescence are organized and operated is essential to decipher the mechanisms of leaf senescence. It was previously reported that the trifurcate feed-forward pathway involving EIN2, ORE1, and miR164 in Arabidopsis regulates age-dependent leaf senescence and cell death. Here, new components of this pathway have been identified, which enhances knowledge of the gene regulatory networks governing leaf senescence. Comparative gene expression analysis revealed six senescence-associated NAC transcription factors (TFs) (ANAC019, AtNAP, ANAC047, ANAC055, ORS1, and ORE1) as candidate downstream components of ETHYLENE-INSENSITIVE2 (EIN2). EIN3, a downstream signalling molecule of EIN2, directly bound the ORE1 and AtNAP promoters and induced their transcription. This suggests that EIN3 positively regulates leaf senescence by activating ORE1 and AtNAP, previously reported as key regulators of leaf senescence. Genetic and gene expression analyses in the ore1 atnap double mutant revealed that ORE1 and AtNAP act in distinct and overlapping signalling pathways. Transient transactivation assays further demonstrated that ORE1 and AtNAP could activate common as well as differential NAC TF targets. Collectively, the data provide insight into an EIN2-mediated senescence signalling pathway that coordinates global gene expression during leaf senescence via a gene regulatory network involving EIN3 and senescence-associated NAC TFs.
叶片衰老 是一个精细调控且由基因编程的退化过程,对于通过将衰老叶片中的养分转运到新发育的器官来最大化植物适应性至关重要。叶片衰老 是一个复杂的过程,由全球基因表达的广泛重编程以高度协调的方式驱动。了解参与控制叶片衰老的基因调控网络是如何组织和运作的,对于破译叶片衰老的机制至关重要。先前有报道称,拟南芥中涉及EIN2、ORE1和miR164的三叉前馈途径调节年龄依赖性叶片衰老和细胞死亡。在这里,已经鉴定出该途径的新成分,这增加了对控制叶片衰老的基因调控网络的了解。比较基因表达分析揭示了六个衰老相关的NAC转录因子(TFs)(ANAC019、AtNAP、ANAC047、ANAC055、ORS1和ORE1)作为乙烯不敏感2(EIN2)的候选下游成分。EIN3是EIN2的下游信号分子,直接结合ORE1和AtNAP启动子并诱导它们的转录。这表明EIN3通过激活ORE1和AtNAP来正向调节叶片衰老,ORE1和AtNAP先前被报道为叶片衰老的关键调节因子。ore1 atnap双突变体的遗传和基因表达分析表明,ORE1和AtNAP在不同且重叠的信号通路中起作用。瞬时反式激活分析进一步证明,ORE1和AtNAP可以激活共同的以及不同的NAC TF靶标。总体而言,这些数据提供了对EIN2介导的衰老信号通路的见解,该通路通过涉及EIN3和衰老相关NAC TFs的基因调控网络在叶片衰老期间协调全球基因表达。