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. 2015 May 8;27(5):1428–1444. doi: 10.1105/tpc.15.00201

Figure 8.

Figure 8.

SDG711 and JMJ703 Are Involved in Histone Modification and Repression of OsCKX2/Gn1a.

(A) Diagram of the CKX2/Gn1a locus. The transcribed region is represented by the thick line. Relative positions of the transcription start site (TSS) and the primer sets (P1 to P4) used in ChIP experiments are indicated.

(B) ChIP assay with anti H3K27me3 (left) and anti H3K4me3 (right) of IM chromatin of wild-type (DJ), SDG711 RNAi, gain-of-function mutant (sdg711), and overexpression (OX) plants.

(C) ChIP assay with anti H3K27me3 (left) and anti H3K4me3 (right) of IM chromatin of SDG711 RNAi, jmj703 mutant, SDG711 and JMJ703 double knockdown/knockout, JMJ703 overexpression plants, and their respective wild-type plants (DJ and ZH11).

(D) SDG711 and JMJ703 were associated directly with CKX2/Gn1a locus. ChIP assays were performed with the same samples as in (B) using anti-SDG711 (left) and with the indicated genotypes using anti-FLAG (right). Anti-IgG was used as controls in the ChIP assays.