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reSETting chromatin during transcription elongation

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Pages 10-15 | Published online: 20 Dec 2012

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Figure 1. Set2-mediated H3K36 methylation and its functional consequences.(A) Set2/Rpd3S pathway. The RNAP II-associated histone methyltransferase Set2 methylates H3K36 (red circle). This mark is recognized by the Rco1 and Eaf3 subunits of the Rpd3S deacetylase complex that maintains genomic regions in a hypoacetylated state by removing acetyl marks (green circle). The arrow indicates the direction of transcription. (B) Distribution of H3K36 methylation (H3K36me), histone exchange and histone acetylation in wild-type or SET2 deleted (set2Δ) yeast strains. (C) Mechanism of Set2-mediated suppression of histone exchange. (i) Co-transcriptional methylation of H3K36 by Set2, results in (ii) preventing Asf1-mediated assembly of newly synthesized pre-acetylated histones (yellow cylinder). (iii) H3K36 methylated nucleosomes are targeted either by the Isw1b complex, or by the RNAP II-associated Chd1 remodeler, resulting in nucleosome remodeling in cis, thus allowing passage of RNAP II and preventing trans-histone exchange by Asf1. (iv) The Rpd3S deacetylase complex is targeted by H3K36 methylation to the coding regions, which is maintained in a hypoacetylated state. (v) The histone chaperone function of Rpd3S may be instrumental in the capture of H3K36 methylated histones and its reassembly following the passage of RNAP II.

Figure 1. Set2-mediated H3K36 methylation and its functional consequences.(A) Set2/Rpd3S pathway. The RNAP II-associated histone methyltransferase Set2 methylates H3K36 (red circle). This mark is recognized by the Rco1 and Eaf3 subunits of the Rpd3S deacetylase complex that maintains genomic regions in a hypoacetylated state by removing acetyl marks (green circle). The arrow indicates the direction of transcription. (B) Distribution of H3K36 methylation (H3K36me), histone exchange and histone acetylation in wild-type or SET2 deleted (set2Δ) yeast strains. (C) Mechanism of Set2-mediated suppression of histone exchange. (i) Co-transcriptional methylation of H3K36 by Set2, results in (ii) preventing Asf1-mediated assembly of newly synthesized pre-acetylated histones (yellow cylinder). (iii) H3K36 methylated nucleosomes are targeted either by the Isw1b complex, or by the RNAP II-associated Chd1 remodeler, resulting in nucleosome remodeling in cis, thus allowing passage of RNAP II and preventing trans-histone exchange by Asf1. (iv) The Rpd3S deacetylase complex is targeted by H3K36 methylation to the coding regions, which is maintained in a hypoacetylated state. (v) The histone chaperone function of Rpd3S may be instrumental in the capture of H3K36 methylated histones and its reassembly following the passage of RNAP II.

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