Department of Biology, University of Copenhagen, Copenhagen, Denmark.
PLoS One. 2010 Sep 7;5(9):e12586. doi: 10.1371/journal.pone.0012586.
Programmed cell death (PCD) is a necessary part of the life of multi-cellular organisms. A type of plant PCD is the defensive hypersensitive response (HR) elicited via recognition of a pathogen by host resistance (R) proteins. The lethal, recessive accelerated cell death 11 (acd11) mutant exhibits HR-like accelerated cell death, and cell death execution in acd11 shares genetic requirements for HR execution triggered by one subclass of R proteins.
METHODOLOGY/PRINCIPAL FINDINGS: To identify genes required for this PCD pathway, we conducted a genetic screen for suppressors of acd11, here called lazarus (laz) mutants. In addition to known suppressors of R protein-mediated HR, we isolated 13 novel complementation groups of dominant and recessive laz mutants. Here we describe laz1, which encodes a protein with a domain of unknown function (DUF300), and demonstrate that LAZ1 contributes to HR PCD conditioned by the Toll/interleukin-1 (TIR)-type R protein RPS4 and by the coiled-coil (CC)-type R protein RPM1. Using a yeast-based topology assay, we also provide evidence that LAZ1 is a six transmembrane protein with structural similarities to the human tumor suppressor TMEM34. Finally, we demonstrate by transient expression of reporter fusions in protoplasts that localization of LAZ1 is distributed between the cytosol, the plasma membrane and FM4-64 stained vesicles.
CONCLUSIONS/SIGNIFICANCE: Our findings indicate that LAZ1 functions as a regulator or effector of plant PCD associated with the HR, in addition to its role in acd11-related death. Furthermore, the similar topology of a plant and human DUF300 proteins suggests similar functions in PCD across the eukaryotic kingdoms, although a direct role for TMEM34 in cell death control remains to be established. Finally, the subcellular localization pattern of LAZ1 suggests that it may have transport functions for yet unknown, death-related signaling molecules at the plasma membrane and/or endosomal compartments. In summary, our results validate the utility of the large-scale suppressor screen to identify novel components with functions in plant PCD, which may also have implications for deciphering cell death mechanisms in other organisms.
细胞程序性死亡(PCD)是多细胞生物生命的必要组成部分。植物 PCD 的一种类型是通过宿主抗性(R)蛋白识别病原体而引发的防御性超敏反应(HR)。致死性、隐性加速细胞死亡 11(acd11)突变体表现出类似于 HR 的加速细胞死亡,并且 acd11 中的细胞死亡执行与由一类 R 蛋白触发的 HR 执行具有遗传要求。
方法/主要发现:为了鉴定该 PCD 途径所需的基因,我们进行了 acd11 的抑制子遗传筛选,这里称为 Lazarus(laz)突变体。除了已知的 R 蛋白介导的 HR 抑制子之外,我们还分离了 13 个新的显性和隐性 laz 突变体的互补群。在这里,我们描述了 laz1,它编码一种具有未知功能域(DUF300)的蛋白质,并证明 LAZ1 有助于 Toll/白细胞介素-1(TIR)型 R 蛋白 RPS4 和卷曲螺旋(CC)型 R 蛋白 RPM1 条件下的 HR PCD。使用酵母基拓扑测定法,我们还提供了证据表明 LAZ1 是一种具有六个跨膜结构域的蛋白质,与人类肿瘤抑制因子 TMEM34 具有结构相似性。最后,我们通过质体中转录报告融合物的瞬时表达证明了 LAZ1 的定位分布在细胞质、质膜和 FM4-64 染色小泡之间。
结论/意义:我们的发现表明,除了在 acd11 相关死亡中起作用外,LAZ1 还作为与 HR 相关的植物 PCD 的调节剂或效应子发挥作用。此外,植物和人类 DUF300 蛋白的相似拓扑结构表明,在真核生物王国中 PCD 具有相似的功能,尽管 TMEM34 在细胞死亡控制中的直接作用仍有待确定。最后,LAZ1 的亚细胞定位模式表明,它可能具有在质膜和/或内体区室中运输未知的与死亡相关的信号分子的功能。总之,我们的结果验证了大规模抑制子筛选在鉴定植物 PCD 新成分中的有效性,这也可能对破译其他生物体的细胞死亡机制具有启示意义。