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. 2014 Sep 8;111(40):14613–14618. doi: 10.1073/pnas.1407131111

Fig. 4.

Fig. 4.

Production and properties of vasiRNAs induced by TuMV-GFP. (A) Northern blot detection of vasiRNAs specific to LHCB1.3 and the antisense 25S rRNA in WT and mutant plants after inoculation with buffer (mock) or TuMV-GFP. Viral genomic RNA and siRNAs as well as miR167 and U6 RNA were also probed. (B) Relative abundance of unique Arabidopsis small RNAs according to their lengths in WT and mutant plants after TuMV-GFP infection. (C) Length distribution and abundance of the total Arabidopsis small RNAs derived from protein-coding genes, rRNAs, tasiRNAs, and transposons from WT and mutant plants after TuMV-GFP infection. (D) Venn diagram depicting the proportion of loci that posses a twofold or greater enrichment of vasiRNAs in WT plants after CMV-∆2b infection and are also enriched twofold or more after TuMV-GFP infection. (E) Distribution pattern of sense (top) and antisense (bottom) vasiRNAs specific to LHCB1.3.