The ubiquitin multi-motif protein UHRF1 is a central player in targeting repressive chromatin marks. It contains a SRA domain, which binds to hemimethylated DNA, a Tudor domain binding to methylated H3 (H3K9me3) and a PHD finger interacting with an unmodified arginine residue within H3 (H3R2) [72–74]. Furthermore, UHRF1 interacts with DNMTs, G9a and HDAC1 and thereby unites various enzymes that can provide a repressive chromatin environment [75–77]. Interestingly, UHRF1 also recruits the H2AK5 actetyltransferase TiP60 thus integrating a multitude of different epigenetic signals [78]. A further example for the link between DNA methylation and histone modifications represent methyl C binding proteins such as MeCP2, which interact with co-repressor complexes including HDACs and HMTs [79,80]. Interestingly, a recent report shows that components of the piRNA pathway are required to target de novo DNA methylation to an imprinted region of the mouse genome implicating that selective methylation of imprinted regions can be regulated by non-coding piRNAs [81].
Imagine 21 pages of this. Okay, 9, if you discount the bibliography. That's the review article we're supposed to read (and understand) for the final part of the Epigenetic Control of Gene Expression MOOC at Melbourne University.
Well… I'm finding it a lot of work to read the text, parse the sentences, expand the abbreviations, and finally integrate it into a whole. I suppose it's mostly due to a lack of training − if I were to read that kind of paper on a daily basis, I guess I would acquire some paper-reading skills. That, or my brain would overheat and melt (and believe me, it's embarrassing to have to mop up your own liquefied brain matter that's dripped through your ear ducts to the carpet.)
I guess I'll have deserved that certificate.
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