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. 2015 Dec 9;15:286. doi: 10.1186/s12870-015-0674-3

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© Hou et al. 2015

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 5 — H3K4me2/3 from NRR, OsWRKY62 and Os-11N3 were increased in jmj704-1. The obtained DNA by anti- H3K4me2/3 ChIP assay was performed for quantitative PCR with primer sets corresponding to transcriptional start site regions of NRR, OsWRKY62 and Os-11N3 (primer sequences seen in Additional file 5: Table S3) in the wild-type (ZH11) and jmj704-1 plants. The genomic region of the genes for ChIP-PCR assay is shown in Additional file 6: Figure S3. Error bars indicate the SD from three biological replicates. Significance of differences was determined by Student’s t tests. *P < 0.05, **P < 0.01