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. 2008 Feb 8;283(6):3006-3010.
doi: 10.1074/jbc.C700192200. Epub 2007 Dec 11.

Arginine methylation of the histone H3 tail impedes effector binding

Aimee N Iberg  1 , Alexsandra Espejo  1 , Donghang Cheng  1 , Daehoon Kim  1 , Jonathan Michaud-Levesque  2 , Stephane Richard  2 , Mark T Bedford  3
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Free article

Arginine methylation of the histone H3 tail impedes effector binding

Aimee N Iberg et al. J Biol Chem. .
Free article

Abstract

Histone tail post-translational modification results in changes in cellular processes, either by generating or blocking docking sites for histone code readers or by altering the higher order chromatin structure. H3K4me3 is known to mark the promoter regions of active transcription. Proteins bind H3K4 in a methyl-dependent manner and aid in the recruitment of histone-remodeling enzymes and transcriptional cofactors. The H3K4me3 binders harbor methyl-specific chromatin binding domains, including plant homeodomain, Chromo, and tudor domains. Structural analysis of the plant homeodomains present in effector proteins, as well as the WD40 repeats of WDR5, reveals critical contacts between residues in these domains and H3R2. The intimate contact between H3R2 and these domain types leads to the hypothesis that methylation of this arginine residue antagonizes the binding of effector proteins to the N-terminal tail of H3. Here we show that H3 tail binding effector proteins are indeed sensitive to H3R2 methylation and that PRMT6, not CARM1/PRMT4, is the primary methyltransferase acting on this site. We have tested the expression of a select group of H3K4 effector-regulated genes in PRMT6 knockdown cells and found that their levels are altered. Thus, PRMT6 methylates H3R2 and is a negative regulator of N-terminal H3 tail binding.

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