Meisel Lee, Fonseca Beatriz, González Susana, Baeza-Yates Ricardo, Cambiazo Veronica, Campos Reinaldo, Gonźalez Mauricio, Orellana Ariel, Retamales Julio, Silva Herman
Laboratorio de Genética Molecular Vegetal, Departamento de Biología, Facultad de Ciencias, Universidad de Chile.
Biol Res. 2005;38(1):83-8. doi: 10.4067/s0716-97602005000100010.
Prunus persica has been proposed as a genomic model for deciduous trees and the Rosaceae family. Optimized protocols for RNA isolation are necessary to further advance studies in this model species such that functional genomics analyses may be performed. Here we present an optimized protocol to rapidly and efficiently purify high quality total RNA from peach fruits (Prunus persica). Isolating high-quality RNA from fruit tissue is often difficult due to large quantities of polysaccharides and polyphenolic compounds that accumulate in this tissue and co-purify with the RNA. Here we demonstrate that a modified version of the method used to isolate RNA from pine trees and the woody plant Cinnamomun tenuipilum is ideal for isolating high quality RNA from the fruits of Prunus persica. This RNA may be used for many functional genomic based experiments such as RT-PCR and the construction of large-insert cDNA libraries.
桃已被提议作为落叶树和蔷薇科的基因组模型。优化的RNA分离方案对于进一步推进该模式物种的研究至关重要,以便能够进行功能基因组学分析。在此,我们提出一种优化方案,可从桃果实(Prunus persica)中快速高效地纯化高质量总RNA。由于果实组织中积累了大量多糖和多酚类化合物并与RNA共纯化,从果实组织中分离高质量RNA通常很困难。在此我们证明,用于从松树和木本植物薄叶樟中分离RNA的方法的改良版本,非常适合从桃果实中分离高质量RNA。这种RNA可用于许多基于功能基因组学的实验,如RT-PCR和大插入片段cDNA文库的构建。