Although miRNAs in plants and animals share many similarities, most mature miRNAs in plants contain 2’-O-methylation at the 3’ end. Typically, ligation of a 3’ adapter via the 3’ OH of the miRNA molecule is the first step in small RNA next-generation sequencing (NGS) sequencing library construction. 2’-O-methylation of plant miRNAs reduces ligation efficiency of the 3’ OH, making plant miRNA libraries difficult to generate.
Here, we show that miRNA profiling from bean, wheat, corn, and rice using total RNA inputs can be successfully achieved using the NEXTflex® Small RNA Sequencing Kit v3, without library purification from PAGE gels, and that extending the ligation incubation step increases library yield. Importantly, many putative novel miRNAs were discovered with the NEXTflex® Small RNA Sequencing Kit v3 that were not discovered using other methods. Thus, this protocol allows generation of reduced-bias small RNA libraries from plant total RNA without the tedious step of gel-based size selection, enabling researchers to discover and profile more small RNAs from more samples than with traditional methods.
https://www.newmarketscientific.com/datasheets/Increasing-Ligation-Efficiency-and-Discovery-of-miRNAs-for-Small-RNA-NGS-Sequencing-Library-Prep-with-Plant-Samples.pdf
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