Figure 4. In the absence of CBR-nucleosome interaction, Hop1 is enriched in centromere regions.
The hop1-loop2 allele is simplified to loop2 in figure labels. (A) Meta-analysis of Hop1 ChIP-seq associated with axis positions in either centromere (defined as any axis site within 20 kb +/− the centromere) or axis positions outside of defined centromere regions. Solid line represents average of axis binding, and shaded region corresponds to 95% confidence intervals. Nonoverlapping confidence intervals are considered to be statistically significant. (B) Hop1 ChIP-seq flanking centromere regions for each chromosome. (C) Same as panel B but for Rec8 ChIP-seq data available for wild type (Sun et al, 2015).
