High-Throughput Screening Identification of Chemical Compounds That Affect Cold-Regulated Gene Expression in Arabidopsis thaliana Using an Excised Single Leaf.

IF 1 Q3 BIOLOGY
Kohei Kitawaki, Ryota Mihara, Yausko Ito-Inaba, Takehito Inaba
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引用次数: 0

Abstract

The identification of chemical compounds that affect intracellular processes has greatly contributed to the understanding of developmental regulation in plants. In this protocol, we describe a method for identifying chemical compounds that affect cold-regulated gene expression in Arabidopsis thaliana. Specifically, we generated Arabidopsis plants harboring a COLD-REGULATED 15A (COR15A) promoter::luciferase (COR15Apro::LUC) construct and grew them in a submerged liquid culture. Using a single true leaf excised from COR15Apro::LUC plants and 96-well culture plates, we performed high-throughput screening of chemical compounds that inhibit cold-induction of COR15Apro::LUC. Luciferase activity was detected using a microplate reader and a chemiluminescence imaging device. This protocol can be easily used for the identification of chemical compounds that regulate other processes, being versatile with respect to equipment. Key features • High-throughput screening of chemical compounds that affect cold-regulated gene expression is possible using a single leaf excised from Arabidopsis grown in a submerged culture. • Screening is based on luciferase activity derived from an excised single leaf. • Direct measurement of luciferase activity is possible using a microplate reader and a chemiluminescence imaging device. • This protocol can be easily used for the identification of chemical compounds that regulate other processes.

高通量筛选鉴定影响拟南芥冷调控基因表达的化合物
对影响细胞内过程的化合物的鉴定极大地促进了对植物发育调控的理解。在本协议中,我们描述了一种方法来鉴定影响拟南芥冷调控基因表达的化合物。具体来说,我们培育了含有COLD-REGULATED 15A (COR15A)启动子::luciferase (COR15Apro::LUC)构建体的拟南芥植株,并将其培养在液体培养液中。利用COR15Apro::LUC植株的单片真叶和96孔培养板,我们对抑制COR15Apro::LUC冷诱导的化合物进行了高通量筛选。荧光素酶活性检测使用微孔板读取器和化学发光成像装置。该协议可以很容易地用于识别调节其他过程的化合物,在设备方面是通用的。高通量筛选影响冷调控基因表达的化合物是可能的,使用从水下培养的拟南芥中切除的单叶。•筛选基于从切除的单叶中提取的荧光素酶活性。使用微孔板读取器和化学发光成像装置可以直接测量荧光素酶活性。•该协议可以很容易地用于识别调节其他过程的化合物。
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来源期刊
CiteScore
1.50
自引率
0.00%
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