University of Potsdam, Institute of Biochemistry and Biology, Karl-Liebknecht-Straβe 24-25, 14476 Potsdam-Golm, Germany.
Mol Plant. 2013 Sep;6(5):1438-52. doi: 10.1093/mp/sst012. Epub 2013 Jan 22.
Senescence is a highly regulated process that involves the action of a large number of transcription factors. The NAC transcription factor ORE1 (ANAC092) has recently been shown to play a critical role in positively controlling senescence in Arabidopsis thaliana; however, no direct target gene through which it exerts its molecular function has been identified previously. Here, we report that BIFUNCTIONAL NUCLEASE1 (BFN1), a well-known senescence-enhanced gene, is directly regulated by ORE1. We detected elevated expression of BFN1 already 2 h after induction of ORE1 in estradiol-inducible ORE1 overexpression lines and 6 h after transfection of Arabidopsis mesophyll cell protoplasts with a 35S:ORE1 construct. ORE1 and BFN1 expression patterns largely overlap, as shown by promoter-reporter gene (GUS) fusions, while BFN1 expression in senescent leaves and the abscission zones of maturing flower organs was virtually absent in ore1 mutant background. In vitro binding site assays revealed a bipartite ORE1 binding site, similar to that of ORS1, a paralog of ORE1. A bipartite ORE1 binding site was identified in the BFN1 promoter; mutating the cis-element within the context of the full-length BFN1 promoter drastically reduced ORE1-mediated transactivation capacity in transiently transfected Arabidopsis mesophyll cell protoplasts. Furthermore, chromatin immunoprecipitation (ChIP) demonstrates in vivo binding of ORE1 to the BFN1 promoter. We also demonstrate binding of ORE1 in vivo to the promoters of two other senescence-associated genes, namely SAG29/SWEET15 and SINA1, supporting the central role of ORE1 during senescence.
衰老(Senescence)是一个高度受调控的过程,涉及大量转录因子的作用。NAC 转录因子 ORE1(ANAC092)最近被证明在拟南芥中正向调控衰老过程中起着关键作用;然而,以前没有鉴定出它发挥其分子功能的直接靶基因。在这里,我们报告双功能核酸酶 1(BFN1),一个众所周知的促进衰老的基因,直接受 ORE1 调控。我们在雌激素诱导的 ORE1 过表达系中,ORE1 诱导后 2 小时,以及在拟南芥叶肉细胞原生质体中瞬时转染 35S:ORE1 构建体 6 小时后,检测到 BFN1 的表达升高。ORE1 和 BFN1 的表达模式高度重叠,如启动子-报告基因(GUS)融合所示,而在 ore1 突变体背景下,衰老叶片和成熟花器官离区中的 BFN1 表达几乎不存在。体外结合位点测定显示出一个二聚体 ORE1 结合位点,类似于 ORE1 的同源物 ORS1。在 BFN1 启动子中鉴定出一个二聚体 ORE1 结合位点;在全长 BFN1 启动子的背景下突变顺式元件,大大降低了瞬时转染的拟南芥叶肉细胞原生质体中 ORE1 介导的转录激活能力。此外,染色质免疫沉淀(ChIP)证明了 ORE1 在体内与 BFN1 启动子的结合。我们还证明了 ORE1 在体内与另外两个与衰老相关的基因 SAG29/SWEET15 和 SINA1 的启动子的结合,支持了 ORE1 在衰老过程中的核心作用。