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. 2005 Jun;25(12):4903–4913. doi: 10.1128/MCB.25.12.4903-4913.2005

FIG. 4.

FIG. 4.

Changes in histone H3 and H4 acetylation are triggered by homologous recombination. A. Cutting and repair of the HO site were measured when the HO endonuclease was induced at 0 h and repressed at 2 h in strain JKM179 (hml/hmrΔ) containing plasmid pGAL-HO-URA3. B. An H3 C-terminal (H3C-term) antibody was used to measure the relative levels of histone proteins 0.6 kb away from the HO site by ChIP, real-time PCR, and statistical analyses as described in the legend to Fig. 2. C. Levels of histone acetylation in strain JKM179 (hml/hmrΔ) containing plasmid pGAL-HO-URA3 at 0.6 kb from the HO site were measured as described for panel B and in the legend to Fig. 2. Significant changes are noted by small light grey circles as described in the legend to Fig. 2.