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首页> 外文期刊>Molecular biology of the cell >A Highlights from MBoC Selection: Chromosome replication and segregation govern the biogenesis and inheritance of inorganic polyphosphate granules
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A Highlights from MBoC Selection: Chromosome replication and segregation govern the biogenesis and inheritance of inorganic polyphosphate granules

机译:MBoC选择的亮点:染色体复制和分离控制着无机多磷酸盐颗粒的生物发生和遗传。

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Prokaryotes and eukaryotes synthesize long chains of orthophosphate, known as polyphosphate (polyP), which form dense granules within the cell. PolyP regulates myriad cellular functions and is often localized to specific subcellular addresses through mechanisms that remain undefined. In this study, we present a molecular-level analysis of polyP subcellular localization in the model bacterium Caulobacter crescentus . We demonstrate that biogenesis and localization of polyP is controlled as a function of the cell cycle, which ensures regular partitioning of granules between mother and daughter. The enzyme polyphosphate kinase 1 (Ppk1) is required for granule production, colocalizes with granules, and dynamically localizes to the sites of new granule synthesis in nascent daughter cells. Localization of Ppk1 within the cell requires an intact catalytic active site and a short, positively charged tail at the C-terminus of the protein. The processes of chromosome replication and segregation govern both the number and position of Ppk1/polyP complexes within the cell. We propose a multistep model in which the chromosome establishes sites of polyP coalescence, which recruit Ppk1 to promote the in situ synthesis of large granules. These findings underscore the importance of both chromosome dynamics and discrete protein localization as organizing factors in bacterial cell biology.
机译:原核生物和真核生物合成正磷酸盐的长链,称为多磷酸盐(polyP),在细胞内形成致密的颗粒。 PolyP调节无数的细胞功能,并通常通过尚不确定的机制定位于特定的亚细胞地址。在这项研究中,我们目前在模型细菌Caulobacter crescentus中对polyP亚细胞定位进行分子水平的分析。我们证明,polyP的生物发生和定位受细胞周期的控制,可确保母子之间的颗粒定期分配。聚磷酸激酶1(Ppk1)酶是生产颗粒所必需的,与颗粒共定位,并动态定位在新生子细胞中新颗粒合成的位点。 Ppk1在细胞内的定位需要完整的催化活性位点和在蛋白质C端的带正电的短尾巴。染色体复制和分离的过程控制着细胞内Ppk1 / polyP复合物的数量和位置。我们提出了一个多步模型,其中染色体建立了polyP聚结位点,该位点募集Ppk1以促进大颗粒的原位合成。这些发现强调了染色体动力学和离散蛋白定位作为细菌细胞生物学中的组织因子的重要性。

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