The subcellular localization and blue-light-induced movement of phototropin 1-GFP in etiolated seedlings of Arabidopsis thalianaW

被引:86
|
作者
Wan, Ying-Lang [2 ]
Eisinger, William [3 ]
Ehrhardt, David [1 ]
Kubitscheck, Ulrich [4 ]
Baluska, Frantisek [2 ]
Briggs, Winslow [1 ]
机构
[1] Carnegie Inst Washington, Dept Plant Biol, Stanford, CA 94305 USA
[2] Univ Bonn, Inst Cellular & Mol Botany, Dept Plant Cell Biol, D-53115 Bonn, Germany
[3] Santa Clara Univ, Dept Biol, Santa Clara, CA 95053 USA
[4] Inst Phys & Theoret Chem, D-53115 Bonn, Germany
基金
美国国家科学基金会;
关键词
D O I
10.1093/mp/ssm011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Phototropin 1 (phot1) 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 phot1 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 best observed 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 phot1 relocalization modulates blue-light-activated signal transduction.
引用
收藏
页码:103 / 117
页数:15
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