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基于双顺反子表达策略的新型荧光计时器在秀丽隐杆线虫中的应用。

A novel fluorescent timer based on bicistronic expression strategy in Caenorhabditis elegans.

机构信息

Key Laboratory of Molecular Biophysics, Ministry of Education, and Institute of Biophysics & Biochemistry, Huazhong University of Science and Technology, Wuhan 430074, PR China.

出版信息

Biochem Biophys Res Commun. 2010 Apr 23;395(1):82-6. doi: 10.1016/j.bbrc.2010.03.143. Epub 2010 Mar 27.

Abstract

Fluorescent timers are useful tools for studying the spatial and temporal cellular or molecular events. Based on the trans-splicing mechanism in Caenorhabditis elegans, we constructed a "fluorescent timer" through bicistronic expression of two fluorescent proteins with different maturation times. When used in vivo, this "timer" changes its color over time and therefore can be used to monitor the activity of the targeted promoters in C. elegans. Using this "timer", we have successfully traced the time-dependent activity of myo-3 promoter which drives expression in body wall muscle and vulval muscle. We found that the myo-3 promoter started to be active about 7 h after egg-laying and sustained its activity in the following hatching process. We have also determined the myo-3 promoter activity during larval development by this "timer". We anticipate that more new "fluorescent timers" with variable time-resolution could be designed by bicistronic expression of different fluorescent protein pairs.

摘要

荧光标记物是研究细胞或分子时空事件的有用工具。基于秀丽隐杆线虫的反式剪接机制,我们通过双顺反子表达两种具有不同成熟时间的荧光蛋白构建了一个“荧光标记物”。当在体内使用时,这个“标记物”会随着时间的推移改变颜色,因此可用于监测线虫中目标启动子的活性。使用这个“标记物”,我们成功地追踪了驱动体壁肌肉和阴道肌肉表达的 myo-3 启动子的时间依赖性活性。我们发现,myo-3 启动子在产卵后约 7 小时开始活跃,并在随后的孵化过程中保持其活性。我们还通过这个“标记物”确定了幼虫发育过程中的 myo-3 启动子活性。我们预计通过不同荧光蛋白对的双顺反子表达,可以设计出更多具有可变时间分辨率的新型“荧光标记物”。

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