A fast and efficient protocol for small RNA extraction in Japanese plum and other Prunus species |
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| Institution: | 1. Laboratorio de Biotecnología, Estación La Platina, Instituto de Investigaciones Agropecuarias, Santa Rosa 11610, La Pintana, Santiago, Chile;2. Biologie du Fruit et Pathologie UMR1332, Centre INRA Bordeaux-Aquitaine, 71 avenue Edouard Bourlaux – CS 20032 - 33882 Villenave d''Ornon Cedex, Bordeaux, France |
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| Abstract: | BackgroundSmall ribonucleic acids represent an important repertoire of mobile molecules that exert key roles in several cell processes including antiviral defense. Small RNA based repertoire includes both small interfering RNA (siRNA) and microRNA (miRNA) molecules. In the Prunus genus, sharka disease, caused by the Plum pox virus (PPV), first occurred on European plum (Prunus domestica) and then spread over among all species in this genus and thus classified as quarantine pathogen. Next-generation sequencing (NGS) was used for the study of siRNA/miRNA molecules; however, NGS relies on adequate extraction protocols. Currently, knowledge of PPV-Prunus interactions in terms of siRNA populations and miRNA species is still scarce, and siRNA/miRNA extraction protocols are limited to species such as peach, almond, and sweet cherry.ResultsWe describe a reliable procedure for siRNA/miRNA purification from Prunus salicina trees, in which previously used protocols did not allow adequate purification. The procedure was based on a combination of commercially available RNA purification kits and specific steps that yielded high quality purifications. The resulting molecules were adequate for library construction and NGS, leading to the development of a pipeline for analysis of both siRNAs and miRNAs in the PPV–P. salicina interactions. Results showed that PPV infection led to altered siRNA profiles in Japanese plum as characterized by decreased 24-nt and increased 21- and 22-nt siRNAs. Infections showed miR164 and miR160 generation and increased miR166, miR171, miR168, miR319, miR157, and miR159.ConclusionWe propose this protocol as a reliable and reproducible small RNA isolation procedure for P. salicina and other Prunus species. |
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