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. 2019 Jul 5;10:2999. doi: 10.1038/s41467-019-10850-5

Fig. 4.

Fig. 4

OsSUF4 and SDG725 enhance the association of each other at target genes. a ChIP analyses at RFT1 and Hd3a promoters using antibodies against OsSUF4, SDG725, and H3K36me3 in WT, suf4Ri-1, 725Ri-1, and suf4Ri-1 725Ri-1 plants, respectively. Upper panel: schematic representation of RFT1 and Hd3a structures and fragments examined in ChIP-PCR. Values are the mean ± SD of three individual biological replicates normalized to the internal control OsUbiquitin5. Asterisks indicate significant differences between indicated genotypes and WT (Student’s t-test: *P < 0.01). b, c CRISPR/Cas9-mediated target mutagenesis of RFT1 and Hd3a, respectively. Upper panel: schematic representation of target site. Nucleotide insertion (shown in blue) resulted in an early stop codon (Red box) for both RFT1 and Hd3a. Left panel: phenotypes of single and double mutants. Right panel: heading date of related plants grown in paddy fields under LD (Shanghai) conditions (b) or SD (Sanya) conditions (c). Values are the mean ± standard deviation for 30 independent plants. Asterisks indicate significant differences between WT and mutants (Student’s t-test: *P < 0.01). Source data are provided as a Source Data file