Supplemental Figure 1. Genes showing ectopic H3K9 dimethylation in this study are DNA hypermethylated in Lister et al. study.
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1 mc mc mc mc SUP mc mc Supplemental Figure. Genes showing ectopic HK9 dimethylation in this study are DNA hypermethylated in Lister et al. study. Representative views of genes that gain HK9m marks in their coding-region in mutants. Representative IGB views (left) and screenshots of the AnnoJ Arabidopsis epigenome browser ( (left) are shown. Yellow horizontal bars: proteincoding genes; blue horizontal bars: transposable elements, green bars: dispersed repeats (i.e. regions of sequence homology); vertical blue bar: relative HK9m levels. Supplemental Figure
2 HK9m ibm atg884 Atg884 Atg4656 HK9m ibm atg4 Atg4 Atg489 HK9m ibm atg67 Atg649 Atg67 Supplemental Figure. Representative views of genes that gain HK9m marks in their body in both ibm and mutants. We observed that HK9m hypermethylation in was usually not as extensive as in ibm in accordance with the idea that these genes may be targets of IBM, the levels of which are reduced in.yellow horizontal bars: protein-coding genes; blue horizontal bars: transposable elements; vertical blue bar: relative HK9m levels. Supplemental Figure
3 A 6 5 Relative HK9m levels 4 Atg549 TA B 5 % overlap with transposons 5 5 genes hypermethylated in genes hypermethylated in ibm all genes everywhere chromosome arms C Supplemental Figure. Supplementary information on Class I genes. A. Verification of HK9m states at genes pre-marked with HK9m in wild type that gain HK9m in (class I genes) by independent chromatin immunoprecipitation experiments. The immunoprecipitated DNA corresponding to a Class I gene (Atg5459) and a transposable element (TA), -shown to be hypermethylated in the ChIP-chip analysis- was quantified by real-time PCR and normalized to the input DNA and to an internal control (actin gene). Class I genes that gain HK9m in have the same response to mutation as some transposable elements such as TA, where HK9m is highly dependant on non-cg methylation. Genomebrowser views of these loci are shown on the right. Yellow horizontal bars: protein-coding genes; blue horizontal bars: transposable elements; green bars: dispersed repeats (regions with sequence of homology); orange bars: small RNAs clusters (MPSS); purple bars: tandem repeats B. Fraction of HK9m hypermethylated genes in that contain a transposable element (TE). C. Representative views of small RNA accumulation at Class I genes in wild type and (Arabidopsis Epigenome Browser, AnnoJ, The translucid reads indicate mapping to multiple locations. Supplemental Figure
4 A HK7m HK9m (-) Atg585-8 atg585-8 Atg4 atg4 At4g899 At5g496 HK7m HK9m (-) Atg899-9 Atg HK7m B 9 HK9m (-) Relative HK9m-DNA levels Atg-5 Atg478 MSH Atg9 Atg899 Atg Atg Atg584ATG589 Supplemental Figure 4. Supplementary information on Class II genes. A. Representative genome-browser views of genes (yellow bars) that gain HK9m marks in their coding-region in and are pre-marked with abundant HK7m in. The green bars represent dispersed repeats which show that these genes (in each box) present sequence homology to each other. Left panels: genes homologous to Atg899 (by their Leucine-rich kinase domains) either linked (ATg9, Blast Score to Atg899 of 5e-9) or unlinked (Atg585 and Atg4, Blast Score to Atg899 of 4e-48 and e-67 respectively). ATg585 is potential sirna-generator locus as shown by the presence of tandem repeats (purple bars) and small RNAs (orange bars). Top right panel: At4g899 is a potential sirna generator locus for At5g496. Bottom left panel: SCPL genes; Atg478 generates sirnas. Middle right panel: in this example, all the loci shown (glycosyl-hydrolase genes) can produce sirnas and could potentially target each other in trans in. B. Verification of HK9m state at Class II genes by independent chromatin immunoprecipitation experiments. The immunoprecipitated DNA was quantified by real-time PCR and normalized to the input DNA and to an internal control (Actin gene). For paralogous genes, only primers that hybridize to gene-specific sequences were used. Supplemental Figure 4
5 A HK7m HK7m HK7m HK9m (-) Atg479 Atg559 Atg595 B HK7m C HK7m HK9m (-) HK9m (-) At4g6 Atg687 Atg6 Atg D Small RNAs (Normalized reads) Supplemental Figure 5. Supplementary information on Class II genes. A. Representative views of genes that gain HK9m in and are HK7m-marked in wild-type; however, these genes were not recovered among Class II genes due to their low levels of HK7m in wild-type. This shows that the number of true Class II genes (HK7m in wild type and ectopic HK9m in ) maybe underestimated by our stringencies. Representative IGB view of genes marked with HK7m marks that do not gain ectopic HK9m in. B. Representative views of genes that are marked with HK7m in but do not gain ectopic HK9m in, suggesting that there are additional features that contribute to ectopic HK9m in. C. Representative genome-browser views of two paralogous or related genes that were not retrieved as dispersed repeats by Repeat Masker, CITRATE SYNTHASE and genes (Atg5874 and Atg5875). These examples suggest that in the genome-wide analysis shown in Figure F, the proportion of genes HK9m hypermethylated in that correspond to duplicated/paralogous/related genes is underestimated and must be larger than 4%. Yellow horizontal bars in IGB views: protein-coding genes; blue horizontal bars: transposable elements; green bars: dispersed repeats (regions with sequence of homology); orange bars: small RNA clusters (MPSS). D. Average distribution of small RNA-seq reads [6] across Class II genes. Supplemental Figure 5
6 A HK7m (-) HK7m (-) HK7m (-) HK7m HK7m HK7m HK7m HK7m HK7m HK9m (-) HK9m (-) HK9m (-) Atg5654 Atg66 Supplemental Figure 6. Supplementary information on HK7m changes in. A. Representative views showing PcG-target genes that do not gain HK9m in, yet lose HK7m marks. B. Global accumulation of HK7m marks in and mutants by Western Blot (upper panel). Detection of histone H -independently of its modifications- is shown as a loading control (lower panel). Supplemental Figure 6
7 .. Relative HK9m-DNA levels suvh456 Relative HK7m-DNA levels suvh456 AtCOPIA4(5') AtMU AtCOPIA4(5') AtMU Supplemental Figure 7. Analysis of HK9m and HK7m marks at two transposons by ChIP followed by real-time PCR. Data were normalized to the input DNA and to an internal control (actin gene). Supplemental Figure 7
8 HK7m HK9m Chr Chr Chr Chr Chr MB Supplemental Figure 8. Chromosomal distributions of HK7m (left) and HK9m (right). Left and right panels show the normalized levels of HK7m and HK9m respectively in a sliding kilobase windows. The black arrow indicates the centromeric region. The blue arrow indicates the heterochromatic knob on chromosome 4. Supplemental Figure 8
9 HK9m-DNA levels (normalized to Input) SUP AGAMOUS Atg899 At4g45 HK7m-DNA levels (normalized to Input) SUP SUP AGAMOUS Atg899 At4g HK9m-DNA levels (normalized to Input) AtROM5 AtCopia8 AtCOPIA4(') suvh HK7m-DNA levels (normalized to Input) AtROM5 AtCopia8 AtCOPIA4(') suvh456 Supplemental Figure 9. Supplementary information on ChIP-chip validation by ChIP-qPCR. Data shown in Figures 4C (top panel) and 5C (bottom panel) are normalized to input, with actin shown as a separate control so that ChIP efficiencies can be visualized. One of the two experiments averaged in Figure C and 4C is shown here as a representative graph. Supplemental Figure 9
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