一种简便高效的从巴西橡胶树胶乳中分离优质RNA的方法

Chaorong Tang, Jiyan Qi, Heping Li, Cunliang Zhang, Yuekun Wang
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引用次数: 102

摘要

从巴西橡胶树乳胶中分离高质量RNA是阐明橡胶树生物合成及其调控分子机制的前提。在这里,改进了乳胶收集、运输、储存和RNA分离的方案。与现有方案相比,我们的方案取消了液氮采集乳胶和低温(- 70℃)条件下的乳胶储存,使得在偏远采样点采集乳胶更加方便可行,而在设备较差的实验室中进行乳胶储存和RNA分离。不同的方法(紫外吸收扫描、变性凝胶电泳、自放射成像监测cDNA合成)证实了该方案制备的RNA的高质量,并通过几个实际应用进一步验证了其有效性,包括构建了一个高质量的cDNA文库,克隆了3个新的橡胶树蔗糖转运蛋白基因的全长cDNA。2个橡胶生物合成必需基因和1个蔗糖转运基因的半定量RT-PCR分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A convenient and efficient protocol for isolating high-quality RNA from latex of Hevea brasiliensis (para rubber tree)

Isolating high-quality RNA from latex of H. brasiliensis is a prerequisite to elucidating the molecular mechanisms of rubber biosynthesis and its regulation. Here, an improved protocol was developed for latex collection, transportation, storage, and RNA isolation. Compared with existing ones, our protocol eliminated liquid nitrogen for latex collection and subsequent low-temperature (− 70 °C) condition for latex storage, making it more convenient and feasible when latex was collected in remote sampling sites, and latex storage and RNA isolation were conducted in poorly-equipped laboratories. Different methods (UV absorbance scans, denaturing gel electrophoresis, autoradiograph monitoring of cDNA synthesis) were used to confirm the high quality of the RNA prepared with this protocol, whose usefulness was further verified by several practical applications, including construction of one high-quality cDNA library, cloning of the full-length cDNAs of 3 novel Hevea sucrose transporter genes, and semi-quantitative RT-PCR analysis of two rubber-biosynthesis essential genes and one sucrose transporter gene.

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