Institute of Biochemistry and Biology, University of Potsdam, Karl-Liebknecht-Straβe 24-25, Haus 20, 14476 Potsdam-Golm, Germany.
Mol Plant. 2011 Mar;4(2):346-60. doi: 10.1093/mp/ssq080. Epub 2011 Feb 8.
We report here that ORS1, a previously uncharacterized member of the NAC transcription factor family, controls leaf senescence in Arabidopsis thaliana. Overexpression of ORS1 accelerates senescence in transgenic plants, whereas its inhibition delays it. Genes acting downstream of ORS1 were identified by global expression analysis using transgenic plants producing dexamethasone-inducible ORS1-GR fusion protein. Of the 42 up-regulated genes, 30 (70%) were previously shown to be up-regulated during age-dependent senescence. We also observed that 32 (76%) of the ORS1-dependent genes were induced by long-term (4 d), but not short-term (6 h) salinity stress (150 mM NaCl). Furthermore, expression of 16 and 24 genes, respectively, was induced after 1 and 5 h of treatment with hydrogen peroxide (H₂O₂), a reactive oxygen species known to accumulate during salinity stress. ORS1 itself was found to be rapidly and strongly induced by H₂O₂ treatment in both leaves and roots. Using in vitro binding site selection, we determined the preferred binding motif of ORS1 and found it to be present in half of the ORS1-dependent genes. ORS1 is a paralog of ORE1/ANAC092/AtNAC2, a previously reported regulator of leaf senescence. Phylogenetic footprinting revealed evolutionary conservation of the ORS1 and ORE1 promoter sequences in different Brassicaceae species, indicating strong positive selection acting on both genes. We conclude that ORS1, similarly to ORE1, triggers expression of senescence-associated genes through a regulatory network that may involve cross-talk with salt- and H₂O₂-dependent signaling pathways.
我们在此报告,ORS1 是 NAC 转录因子家族的一个此前未被描述的成员,它控制着拟南芥的叶片衰老。ORS1 的过表达加速了转基因植物的衰老,而其抑制则延迟了衰老。通过使用产生地塞米松诱导型 ORS1-GR 融合蛋白的转基因植物进行全局表达分析,鉴定了 ORS1 下游的基因。在 42 个上调基因中,有 30 个(约 70%)在年龄相关的衰老过程中被证明是上调的。我们还观察到,32 个(约 76%)的 ORS1 依赖性基因被长期(4 天)但不是短期(6 小时)盐胁迫(150mM NaCl)诱导。此外,分别有 16 和 24 个基因在过氧化氢(H₂O₂)处理 1 和 5 小时后表达,H₂O₂是在盐胁迫期间积累的一种活性氧。ORS1 本身在叶片和根中都被 H₂O₂处理迅速且强烈地诱导。通过体外结合位点选择,我们确定了 ORS1 的首选结合基序,并发现它存在于一半的 ORS1 依赖性基因中。ORS1 是 ORE1/ANAC092/AtNAC2 的同源物,后者是先前报道的叶片衰老调节剂。系统发育足迹分析显示,不同芸薹属物种中 ORS1 和 ORE1 启动子序列的进化保守性,表明这两个基因都受到强烈的正选择。我们的结论是,ORS1 与 ORE1 相似,通过一个可能涉及与盐和 H₂O₂依赖的信号通路交叉对话的调控网络,触发衰老相关基因的表达。