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Colocalization of plastid division proteins in the chloroplast stromalcompartment establishes a new functional relationship between FtsZ1 andFtsZ2 in higher plants

机译:叶绿体基质隔室中质体分裂蛋白的共定位在高等植物中建立了FtsZ1和FtsZ2之间的新功能关系

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Chloroplast division is driven by a macromolecular complex containing components that are positioned on the cytosolic surface of the outer envelope, the stromal surface of the inner envelope, and in the intermembrane space. The only constituents of the division apparatus identified thus far are the tubulin-like proteins FtsZ1 and FtsZ2, which colocalize to rings at the plastid division site. However, the precise positioning of these rings relative to the envelope membranes and to each other has not been previously defined. Using newly isolated cDNAs with open reading frames longer than those reported previously, we demonstrate here that both FtsZ2 proteins in Arabidopsis, like FtsZ1 proteins, contain cleavable transit peptides that target them across the outer envelope membrane. To determine their topological arrangement, protease protection experiments designed to distinguish between stromal and intermembrane space localization were performed on both in vitro imported and endogenous forms of FtsZ1 and FtsZ2. Both proteins were shown to reside in the stromal compartment of the chloroplast, indicating that the FtsZ1- and FtsZ2-containing rings have similar topologies and may physically interact. Consistent with this hypothesis, double immunofluorescence labeling of various plastid division mutants revealed precise colocalization of FtsZ1 and FtsZ2, even when their levels and assembly patterns were perturbed. Overexpression of FtsZ2 in transgenic Arabidopsis inhibited plastid division in a dose-dependent manner, suggesting that the stoichiometry between FtsZ1 and FtsZ2 is an important aspect of their function. These studies raise new questions concerning the functional and evolutionary significance of two distinct but colocalized forms of FtsZ in plants and establish a revised framework within which to understand the molecular architecture of the plastid division apparatus in higher plants.
机译:叶绿体的分裂是由大分子复合物驱动的,大分子复合物包含位于外部包膜的胞质表面,内部包膜的基质表面以及膜间空间中的组分。迄今为止,鉴定出的分离装置的唯一组成是微管蛋白样蛋白FtsZ1和FtsZ2,它们共定位在质体分裂位点的环上。然而,这些环相对于包膜以及彼此的精确定位尚未预先定义。使用具有比以前报道的更长的开放阅读框的新分离的cDNA,我们在这里证明拟南芥中的FtsZ2蛋白和FtsZ1蛋白一样都含有可切割的转运肽,这些肽靶向它们穿过外膜。为了确定它们的拓扑结构,对FtsZ1和FtsZ2的体外导入和内源形式进行了旨在区分基质和膜间空间定位的蛋白酶保护实验。两种蛋白质均显示位于叶绿体的基质区室中,表明含有FtsZ1和FtsZ2的环具有相似的拓扑结构,并且可能发生物理相互作用。与此假设一致,各种质体分裂突变体的双重免疫荧光标记揭示了FtsZ1和FtsZ2的精确共定位,即使它们的水平和装配模式受到干扰也是如此。 FtsZ2在转基因拟南芥中的过表达以剂量依赖的方式抑制了质体分裂,这表明FtsZ1和FtsZ2之间的化学计量是其功能的重要方面。这些研究提出了关于植物中两种不同但共存的FtsZ形式的功能和进化意义的新问题,并建立了一个修订的框架,以了解高等植物中质体分裂装置的分子结构。

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