Moazzam Jazi Maryam, Rajaei Saideh, Seyedi Seyed Mahdi
Plant Biotechnology Department, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.
Environmental and Industrial Biotechnology Department, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.
Physiol Mol Biol Plants. 2015 Oct;21(4):597-603. doi: 10.1007/s12298-015-0319-x. Epub 2015 Oct 7.
The quality and quantity of RNA are critical for successful downstream transcriptome-based studies such as microarrays and RNA sequencing (RNA-Seq). RNA isolation from woody plants, such as Pistacia vera, with very high amounts of polyphenols and polysaccharides is an enormous challenge. Here, we describe a highly efficient protocol that overcomes the limitations posed by poor quality and low yield of isolated RNA from pistachio and various recalcitrant woody plants. The key factors that resulted in a yield of 150 μg of high quality RNA per 200 mg of plant tissue include the elimination of phenol from the extraction buffer, raising the concentration of β-mercaptoethanol, long time incubation at 65 °C, and nucleic acid precipitation with optimized volume of NaCl and isopropyl alcohol. Also, the A260/A280 and A260/A230 of extracted RNA were about 1.9-2.1and 2.2-2.3, respectively, revealing the high purity. Since the isolated RNA passed highly stringent quality control standards for sensitive reactions, including RNA sequencing and real-time PCR, it can be considered as a reliable and cost-effective method for RNA extraction from woody plants.
RNA的质量和数量对于基于转录组的下游研究(如微阵列和RNA测序(RNA-Seq))的成功至关重要。从含有大量多酚和多糖的木本植物(如阿月浑子)中分离RNA是一项巨大的挑战。在此,我们描述了一种高效方案,该方案克服了从开心果和各种难处理木本植物中分离的RNA质量差和产量低所带来的限制。每200毫克植物组织能产生150微克高质量RNA的关键因素包括从提取缓冲液中去除苯酚、提高β-巯基乙醇的浓度、在65℃下长时间孵育以及用优化体积的NaCl和异丙醇进行核酸沉淀。此外,提取的RNA的A260/A280和A260/A230分别约为1.9 - 2.1和2.2 - 2.3,表明纯度很高。由于分离的RNA通过了包括RNA测序和实时PCR在内的敏感反应的高度严格质量控制标准,因此它可被视为一种从木本植物中提取RNA的可靠且经济高效的方法。