The RITS complex binds chromatin via the chromodomain protein Chp1 and recruits the CLRC complex to the centromeric repeats via the linker protein Stc1. Clr4, a component of the CLRC, is the only histone methyltransferase which methylates H3 on lysine 9 in fission yeast. H3K9 methylation creates a binding site for the chromodomain proteins Swi6, Chp1 and Chp2, which are required for the spreading of heterochromatin and the binding of RITS to chromatin. Swi6 and Chp2 are orthologs of HP1 which binds H3K9 methylated chromatin in metazoa. In addition to Clr4, the CLRC complex consists of the cullin scaffold protein Cul4, the b-propeller protein Rik1, the RING box protein Rbx1, the WD-40 protein Raf1/Dos1 and Raf2/Dos2. We have previously shown that members of the CLRC complex are EED226 predicted to adopt a structure similar to the conserved Cul4-DDB1-DDB2 E3 ubiquitin ligase and recent structural analysis of Raf1 has confirmed this prediction. In addition, the CLRC complex has been shown to possess E3 ligase activity in vitro. Although CLRC has been the subject of extensive study, the role of the Raf2 subunit within this complex and its Acetohexamide contribution to heterochromatin formation remains elusive. In addition to its association with CLRC, Raf2 has been proposed to regulate transcription within heterochromatin during S phase via its interaction with Cdc20 and the transcription factor Mms19 at replication forks. Moreover, Raf2 has recently been implicated in the localisation of the CENP-ACnp1 histone H3 variant to centromeres. Raf2 contains a C2H2 type zinc finger and an N-terminal region which exhibits similarity to the Replication Foci Targeting Sequence domain found in the DNA methyltransferase DNMT1. The RFTS domain is conserved across fungi, plants and animals but only the RFTS domain of mammalian DNMT1 has been characterised. DNMT1 is the major enzyme responsible for the maintenance of the typically repressive DNA modification in plant and vertebrate cytosine methylation of CpG dinucleotides. The RFTS domain of DNMT1 has been implicated in its catalytic function, protein interactions and subcellular localisation.