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The Arabidopsis repressor of light signaling, COP1, is regulated by nuclear exclusion: Mutational analysis by bioluminescence resonance energy transfer

机译:光信号的拟南芥阻遏物,COP1,是通过核排斥来调节的:通过生物发光共振能量转移进行突变分析

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摘要

Bioluminescence resonance energy transfer (BRET) between Renilla luciferase and yellow fluorescent protein has been adapted to serve as a real-time reporter on protein-protein interactions in live plant cells by using the Arabidopsis Constitutive photomorphogenesis 1 (COP1) protein as a model system. COP1 is a repressor of light signal transduction that functions as part of a nuclear E3 ubiquitin ligase. COP1 possesses a leucine-rich nuclear-exclusion signal that resides in a domain implicated in COP1 dimerization. BRET was applied in conjunction with site-directed mutagenesis to explore the respective contributions of the nuclear-exclusion and dimerization motifs to the regulation of COP1 activity in vivo. One specific mutant protein, COP1L105A, showed increased nuclear accumulation but retained the ability to dimerize, as monitored by BRET, whereas other mutations inhibited both nuclear exclusion and COP1 dimerization. Mutant rescue and overexpression experiments indicated that nuclear exclusion of COP1 protein is a rate-limiting step in light signal transduction.
机译:通过使用拟南芥组成型光形态发生1(COP1)蛋白作为模型系统,使海藻荧光素酶和黄色荧光蛋白之间的生物发光共振能量转移(BRET)可以充当活植物细胞中蛋白质-蛋白质相互作用的实时报告者。 COP1是光信号转导的阻遏物,其功能是核E3泛素连接酶的一部分。 COP1具有富含亮氨酸的核排斥信号,该信号位于与COP1二聚化有关的域中。 BRET与定点诱变结合使用,以探讨核排斥和二聚体基序对体内COP1活性调节的各自贡献。如BRET所监测,一种特定的突变蛋白COP1L105A显示出增加的核蓄积,但保留了二聚化的能力,而其他突变则抑制了核排斥和COP1二聚化。突变抢救和过表达实验表明,COP1蛋白的核排斥是光信号转导中的限速步骤。

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