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环磷酸腺苷缺乏对烟草Bright Yellow-2细胞的细胞生长产生负面影响,并增强与应激相关的反应。

Cyclic AMP deficiency negatively affects cell growth and enhances stress-related responses in tobacco Bright Yellow-2 cells.

作者信息

Sabetta Wilma, Vannini Candida, Sgobba Alessandra, Marsoni Milena, Paradiso Annalisa, Ortolani Francesca, Bracale Marcella, Viggiano Luigi, Blanco Emanuela, de Pinto Maria Concetta

机构信息

Istituto di Bioscienze e Biorisorse, CNR, Via G. Amendola 165/A, 70126, Bari, Italy.

Dipartimento di Biotecnologie e Scienze della Vita, Università degli Studi dell'Insubria, Via H. J. Dunant 3, 21100, Varese, Italy.

出版信息

Plant Mol Biol. 2016 Mar;90(4-5):467-83. doi: 10.1007/s11103-016-0431-5. Epub 2016 Jan 19.

Abstract

Cyclic adenosine 3',5'-monophosphate (cAMP) is a recognized second messenger; however, knowledge of cAMP involvement in plant physiological processes originates primarily from pharmacological studies. To obtain direct evidence for cAMP function in plants, tobacco Bright Yellow-2 (BY-2) cells were transformed with the cAMP sponge, which is a genetically encoded tool that reduces cAMP availability. BY-2 cells expressing the cAMP sponge (cAS cells), showed low levels of free cAMP and exhibited growth inhibition that was not proportional to the cAMP sponge transcript level. Growth inhibition in cAS cells was closely related to the precocious inhibition of mitosis due to a delay in cell cycle progression. The cAMP deficiency also enhanced antioxidant systems. Remarkable changes occurred in the cAS proteomic profile compared with that of wild-type (WT) cells. Proteins involved in translation, cytoskeletal organization, and cell proliferation were down-regulated, whereas stress-related proteins were up-regulated in cAS cells. These results support the hypothesis that BY-2 cells sense cAMP deficiency as a stress condition. Finally, many proteasome subunits were differentially expressed in cAS cells compared with WT cells, indicating that cAMP signaling broadly affects protein degradation via the ubiquitin/proteasome pathway.

摘要

环磷腺苷(cAMP)是一种公认的第二信使;然而,关于cAMP参与植物生理过程的知识主要来源于药理学研究。为了获得cAMP在植物中功能的直接证据,用cAMP海绵体转化烟草亮黄-2(BY-2)细胞,cAMP海绵体是一种可减少cAMP可用性的基因编码工具。表达cAMP海绵体的BY-2细胞(cAS细胞)显示出低水平的游离cAMP,并表现出生长抑制,且这种抑制与cAMP海绵体转录水平不成比例。cAS细胞中的生长抑制与由于细胞周期进程延迟导致的有丝分裂早熟抑制密切相关。cAMP缺乏还增强了抗氧化系统。与野生型(WT)细胞相比,cAS细胞的蛋白质组学图谱发生了显著变化。参与翻译、细胞骨架组织和细胞增殖的蛋白质在cAS细胞中下调,而与应激相关的蛋白质在cAS细胞中上调。这些结果支持了BY-2细胞将cAMP缺乏感知为应激条件的假说。最后,与WT细胞相比,许多蛋白酶体亚基在cAS细胞中差异表达,表明cAMP信号通过泛素/蛋白酶体途径广泛影响蛋白质降解。

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