Laboratory of Genetics and Plant Improvement, Department of Agronomy, Centre for Agricultural Sciences and Engineering, Federal University of Espírito Santo, Alegre, ES, Brazil.
PLoS One. 2021 Jul 26;16(7):e0255245. doi: 10.1371/journal.pone.0255245. eCollection 2021.
Acquiring high-quality RNA in sufficient amounts is crucial in plant molecular biology and genetic studies. Several methods for RNA extraction from plants are available in the literature, mainly due to the great biochemical diversity present in each species and tissue, which can complicate or prevent the extraction. Psidium guajava (Myrtaceae family) is a perennial fruit tree of medicinal and economic value; nevertheless, only a few molecular studies are available for the species. One reason is the difficulty in obtaining RNA due to the content of the samples, which are rich in polyphenols, polysaccharides, and secondary metabolites. Furthermore, there are few studies available for the isolation of RNA from guava or Psidium samples, which hampers advances in the study of the genus. Here, quality and yields of RNA isolates were compared using six extraction protocols: two protocols based on the application of cetyltrimethylammonium bromide (CTAB) lysis buffer, one protocol which uses the TRIzol reagent, one which applies guanidine thiocyanate lysis buffer followed by organic phase extraction, and two commercial kits (PureLink RNA Mini Kit and RNeasy Plant Mini Kit). The CTAB-based method provided the highest RNA yields and quality for five different tissues (flower bud, immature leaf, young leaf, mature leaf, and root), genotypes, and stress conditions. For the most efficient protocol, the average yield of RNA from guava leaves was 203.06 μg/g of tissue, and the A260/A280 and A260/A230 ratios were 2.1 and 2.2, respectively. RT-qPCR analysis demonstrated that the purity of the samples was sufficient for molecular biology experiments. CTAB-based methods for RNA isolation were found to be the most efficient, providing the highest RNA yields and quality for tissues from P. guajava. Additionally, they were compatible for downstream RNA-based applications, besides being simple and cost-effective.
在植物分子生物学和遗传学研究中,获取高质量且足够量的 RNA 至关重要。文献中提供了几种从植物中提取 RNA 的方法,这主要是由于每个物种和组织都存在巨大的生化多样性,这可能会使提取变得复杂或受阻。番石榴(桃金娘科)是一种具有药用和经济价值的多年生果树;然而,针对该物种的分子研究却很少。原因之一是由于样本中富含多酚、多糖和次生代谢物,导致 RNA 难以获得。此外,从番石榴或 Psidium 样本中分离 RNA 的研究很少,这阻碍了该属的研究进展。在这里,使用六种提取方案比较了 RNA 分离物的质量和产量:两种基于十六烷基三甲基溴化铵 (CTAB) 裂解缓冲液应用的方案,一种使用 TRIzol 试剂的方案,一种应用硫氰酸胍裂解缓冲液后进行有机相萃取的方案,以及两种商业试剂盒(PureLink RNA Mini Kit 和 RNeasy Plant Mini Kit)。基于 CTAB 的方法为五个不同组织(花蕾、未成熟叶、幼叶、成熟叶和根)、基因型和胁迫条件提供了最高的 RNA 产量和质量。对于最有效的方案,番石榴叶的平均 RNA 产量为 203.06μg/g 组织,A260/A280 和 A260/A230 比值分别为 2.1 和 2.2。RT-qPCR 分析表明,样品的纯度足以进行分子生物学实验。基于 CTAB 的 RNA 分离方法被发现是最有效的方法,为番石榴组织提供了最高的 RNA 产量和质量。此外,它们还与下游基于 RNA 的应用兼容,同时简单且具有成本效益。