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. 2014 Oct 31;11(9):1180–1188. doi: 10.4161/rna.36281

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© 2014 The Author(s). Published with license by Taylor & Francis Group, LLC

This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.

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Figure 1. — Distribution of m⁶A modification peaks along mRNA and chromosome (A) Transcriptome-wide distribution of m⁶A peaks. Bar graph shows the fraction of m⁶A peaks in each of the 5 non-overlapping transcript segments. (B) Distribution of m⁶A peaks across the length of mRNAs. 5′UTRs, CDS, and 3′UTRs of rice mRNAs are individually binned into regions spanning 1% of their total length, and the percentage of m⁶A peaks that fall within each bin is determined. (C)Distribution of m⁶A peaks along chromosomes of callus and leaf tissues. From top to bottom, 3 horizontal bars represent chromosomes, where the m⁶A peak density in callus, leaf, TE gene and expressed gene (taking callus as samples) in 500-kb windows are displayed with scales as indicated. Diamonds in different colors (light blue->green-> brown->purple) represent numbers of peaks or genes ascending.