Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2020 Jun 12;10:9540. doi: 10.1038/s41598-020-66374-2

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

Genome-wide distribution of TuMV-derived siRNAs in wild type Arabidopsis thaliana and de-novo assembly of the TuMV genome. 21- to 24-nt virus-derived siRNAs were pooled and correspond to samples in Fig. 1. Abundance was normalized to reads per million. (a) Genome-wide distribution of TuMV-derived siRNAs by match class in inoculated rosette leaves and in systemically infected inflorescence. (b) Abundance of siRNAs with one or two mismatches relative to siRNAs with no mutations. (c) Relationship between siRNAs of positive and negative polarity and containing mutations. (d) De-novo assembly of the TuMV genome using virus-derived siRNAs without mutations. Lines represent contigs and red arrowheads point to gaps in the assembly. In this TuMV clone, HC-Pro is marked with 6xHIS at the N terminus²⁷.