研究蓝藻 Synechocystis PCC 6803 中的单氧响应基因。

IF 5.4 2区 生物学 Q1 PLANT SCIENCES Physiologia plantarum Pub Date : 2024-07-01 DOI:10.1111/ppl.14468
Gábor Patyi, Barbara Hódi, Ivy Mallick, Gergely Maróti, Péter B Kós, Imre Vass
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引用次数: 0

摘要

单线态氧(1O2)是一种重要的活性氧,它在光合作用过程中不可避免地会通过依赖光的 II 型光动力反应形成。在过去的几十年中,人们认识到 1O2 不仅是一种破坏性物质,还能影响基因表达并参与信号转导途径,这一点受到越来越多的关注。然而,与其他几个类群相反,在重要的蓝藻模式生物 Synechocystis PCC 6803 中尚未发现 1O2 响应基因。通过全局转录本分析,我们确定了一大批 Synechocystis 基因,它们的转录本水平在 1O2 存在时要么增强,要么抑制。在 Synechocystis 的几个光诱导基因中观察到了特征性的 1O2 反应,尤其是在编码参与光保护的 HLIP/SCP 蛋白的 hli(或 scp)家族中。其他重要的 1O2 诱导基因包括光系统 II 修复机制(psbA2 和 ftsH2、ftsH3)、铁稳态基因 isiA 和 idiA、第 2 组 sigma 因子 sigD、盐胁迫、高渗胁迫和冷胁迫诱导的转录组中的一些成分,以及一些功能未知的基因。1O2 诱导的上调最明显的是 hliB 和共转录的 lilA 基因,删除这两个基因会提高对 1O2 介导的光损伤的敏感性。通过将 hliB 启动子与细菌荧光素酶(lux)融合,产生了一种生物报告器 Synechocystis 菌株,该菌株可用于持续监测细胞内的 1O2 浓度。
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Investigation of singlet-oxygen-responsive genes in the cyanobacterium Synechocystis PCC 6803.

Singlet oxygen (1O2) is an important reactive oxygen species whose formation by the type-II, light-dependent, photodynamic reaction is inevitable during photosynthetic processes. In the last decades, the recognition that 1O2 is not only a damaging agent, but can also affect gene expression and participates in signal transduction pathways has received increasing attention. However, contrary to several other taxa, 1O2-responsive genes have not been identified in the important cyanobacterial model organism Synechocystis PCC 6803. By using global transcript analysis we have identified a large set of Synechocystis genes, whose transcript levels were either enhanced or repressed in the presence of 1O2. Characteristic 1O2 responses were observed in several light-inducible genes of Synechocystis, especially in the hli (or scp) family encoding HLIP/SCP proteins involved in photoprotection. Other important 1O2-induced genes include components of the Photosystem II repair machinery (psbA2 and ftsH2, ftsH3), iron homeostasis genes isiA and idiA, the group 2 sigma factor sigD, some components of the transcriptomes induced by salt-, hyperosmotic and cold-stress, as well as several genes of unknown function. The most pronounced 1O2-induced upregulation was observed for the hliB and the co-transcribed lilA genes, whose deletion induced enhanced sensitivity against 1O2-mediated light damage. A bioreporter Synechocystis strain was created by fusing the hliB promoter to the bacterial luciferase (lux), which showed its utility for continuous monitoring of 1O2 concentrations inside the cell.

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来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
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