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The Subcellular Localization and Blue-Light- Induced Movement of Phototropin 1-GFP in Etiolated Seedlings of Arabidopsis thaliana

机译:亚光定位拟南芥幼苗的光化蛋白1-GFP的亚细胞定位和蓝光诱导的运动。

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Phototropin 1 (phott) is a photoreceptor for phototropism, chloroplast movement, stomatal opening, leaf expansion, and solar tracking in response to blue light. Following earlier work with PHOT1::GFP (Sakamoto and Briggs, 2002), we investigated the pattern of cellular and subcellular localization of phot! in 3-4 d old etiolated seedlings of Arabidopsis thalinana. As expressed from native upstream sequences, the PHOT1::GFP fusion protein is expressed strongly in the abaxial tissues of the cotyledons and in the elongating regions of the hypocotyl. it is moderately expressed in the shoot/root transition zone and in cells near the root apex. A fluorescence signal is undetectable in the root epidermis, root cap, and root apical meristem itself. The plasma membranes of mesophyll cells near the cotyledon margin appear labeled uniformly but cross-walls created by recent cell divisions are more strongly labeled. The pattern of labeling of individual cell types varies with cell type and developmental stage.Blue-light treatment causes PHOT1::GFP, initially relatively evenly distributed at the plasma membrane, to become reorganized into a,distinct mosaic with strongly labeled punctate areas and other areas completely devoid of fluorescence—a phenomenon bestobserved in cortical cells in the hypocotyl elongation region. Concomitant with or following this reorganization, PHOT1::GFP moves into the cytoplasm in all cell types investigated except for guard cells. It disappears from the cytoplasm by an unidentified mechanism after several hours in darkness. Neither its appearance in the cytoplasm nor its eventual disappearance in darkness is prevented by the translation inhibitor cycloheximide, although the latter process is retarded. We hypothesize that blue-light-induced photl re-localization modulates blue-light-activated signal transduction.
机译:Phototropin 1(phott)是一种感光细胞,用于响应蓝光,具有向光性,叶绿体运动,气孔张开,叶片膨胀和日光跟踪。在对PHOT1 :: GFP进行早期工作之后(Sakamoto和Briggs,2002年),我们研究了phot!的细胞和亚细胞定位模式。在3-4天拟南芥的黄化老苗中。如从天然上游序列表达的,PHOT1 :: GFP融合蛋白在子叶的背面组织和下胚轴的延伸区域中强烈表达。在芽/根过渡区和根尖附近的细胞中适度表达。在根表皮,根冠和根尖分生组织本身中无法检测到荧光信号。子叶边缘附近的叶肉细胞的质膜似乎被均匀地标记,但是由最近的细胞分裂产生的跨壁被更强烈地标记。单个细胞类型的标记模式随细胞类型和发育阶段而变化。蓝光处理导致最初在质膜上相对均匀分布的PHOT1 :: GFP重组为具有明显标记点状区域和其他斑点的马赛克完全没有荧光的区域-在下胚轴延伸区的皮质细胞中观察到的现象最好。在重组过程的同时或之后,除保卫细胞外,PHOT1 :: GFP进入所有研究的细胞类型的细胞质。在黑暗中几个小时后,它以未知机制从细胞质中消失。尽管后者的过程受阻,但翻译抑制剂环己酰亚胺并不能阻止其在细胞质中的出现或在黑暗中的最终消失。我们假设,蓝光诱导的磷酸化重新定位调节了蓝光激活的信号转导。

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    《Molecular Plant》 |2008年第1期|共15页
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  • 正文语种 eng
  • 中图分类 生物科学;
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