Xu Xianfeng Morgan, Zhao Qiao, Rodrigo-Peiris Thushani, Brkljacic Jelena, He Chao Sylvia, Müller Sabine, Meier Iris
Plant Biotechnology Center and Department of Plant Cellular and Molecular Biology, The Ohio State University, Columbus, OH 43210, USA.
Proc Natl Acad Sci U S A. 2008 Nov 25;105(47):18637-42. doi: 10.1073/pnas.0806157105. Epub 2008 Nov 14.
In higher plants, the plane of cell division is faithfully predicted by the preprophase band (PPB). The PPB, a cortical ring of microtubules and F-actin, disassembles upon nuclear-envelope breakdown. During cytokinesis, the expanding cell plate fuses with the plasma membrane at the cortical division site, the site of the former PPB. The nature of the "molecular memory" that is left behind by the PPB and is proposed to guide the cell plate to the cortical division site is unknown. RanGAP is the GTPase activating protein of the small GTPase Ran, which provides spatial information for nucleocytoplasmic transport and various mitotic processes in animals. Here, we show that, in dividing root cells, Arabidopsis RanGAP1 concentrates at the PPB and remains associated with the cortical division site during mitosis and cytokinesis, requiring its N-terminal targeting domain. In a fass/ton2 mutant, which affects PPB formation, RanGAP1 recruitment to the PPB site is lost, while its PPB retention is microtubule-independent. RanGAP1 persistence at the cortical division site, but not its initial accumulation at the PPB requires the 2 cytokinesis-regulating kinesins POK1 and POK2. Depletion of RanGAP by inducible RNAi leads to oblique cell walls and cell-wall stubs in root cell files, consistent with cytokinesis defects. We propose that Arabidopsis RanGAP, a continuous positive protein marker of the plant division plane, has a role in spatial signaling during plant cell division.
在高等植物中,细胞分裂平面由早前期带(PPB)准确预测。PPB是微管和F-肌动蛋白构成的皮质环,在核膜破裂时解体。在胞质分裂期间,扩展的细胞板在皮质分裂位点与质膜融合,该位点即先前PPB的位置。由PPB留下并被认为引导细胞板至皮质分裂位点的“分子记忆”的本质尚不清楚。RanGAP是小GTP酶Ran的GTP酶激活蛋白,它为动物中的核质运输和各种有丝分裂过程提供空间信息。在这里,我们表明,在分裂的根细胞中,拟南芥RanGAP1集中在PPB处,并在有丝分裂和胞质分裂期间与皮质分裂位点保持关联,这需要其N端靶向结构域。在影响PPB形成的fass/ton2突变体中,RanGAP1募集到PPB位点的过程丧失,而其在PPB处的保留不依赖于微管。RanGAP1在皮质分裂位点的持续存在,而非其在PPB处的初始积累,需要两种胞质分裂调节驱动蛋白POK1和POK2。通过诱导性RNA干扰耗尽RanGAP会导致根细胞列中的倾斜细胞壁和细胞壁残端,这与胞质分裂缺陷一致。我们提出,拟南芥RanGAP作为植物分裂平面的连续阳性蛋白标记物,在植物细胞分裂过程中的空间信号传导中发挥作用。