Type I Arginine Methyltransferases PRMT1 and PRMT-3 Act Distributively

Asymmetric dimethylation of arginine residues is a common posttranslational modification of proteins carried out by type I protein arginine methyltransferases, including PRMT1 and -3. We report that the consecutive transfer of two methyl groups to a single arginine side chain by PRMT1 and -3 occurs...

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Veröffentlicht in:The Journal of biological chemistry 2009-03, Vol.284 (13), p.8274-8282
Hauptverfasser: Kölbel, Knut, Ihling, Christian, Bellmann-Sickert, Kathrin, Neundorf, Ines, Beck-Sickinger, Annette G., Sinz, Andrea, Kühn, Uwe, Wahle, Elmar
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container_end_page 8282
container_issue 13
container_start_page 8274
container_title The Journal of biological chemistry
container_volume 284
creator Kölbel, Knut
Ihling, Christian
Bellmann-Sickert, Kathrin
Neundorf, Ines
Beck-Sickinger, Annette G.
Sinz, Andrea
Kühn, Uwe
Wahle, Elmar
description Asymmetric dimethylation of arginine residues is a common posttranslational modification of proteins carried out by type I protein arginine methyltransferases, including PRMT1 and -3. We report that the consecutive transfer of two methyl groups to a single arginine side chain by PRMT1 and -3 occurs in a distributive manner, i.e. with intermittent release of the monomethylated intermediate. The oligomeric state of PRMTs together with the clustering of methylated arginine residues in most proteins carrying this type of modification suggests that multiple methyl transfers to a single polypeptide chain might proceed in a processive manner by cooperation of multiple active sites. However, three different types of experiments provide evidence that the reaction is distributive even with substrates containing multiple methyl-accepting arginines, including one with 13 such residues. PRMT1 also does not prefer substrates already containing one or more singly or doubly methylated arginine residues. Even though the reaction is distributive, the efficiency of methylation of one particular protein strongly depends on the number of methyl-accepting arginine residues it contains.
doi_str_mv 10.1074/jbc.M809547200
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subjects Animals
Arginine - chemistry
Arginine - genetics
Arginine - metabolism
Humans
Methylation
Protein Processing, Post-Translational - physiology
Protein Synthesis, Post-Translational Modification, and Degradation
Protein-Arginine N-Methyltransferases - chemistry
Protein-Arginine N-Methyltransferases - genetics
Protein-Arginine N-Methyltransferases - metabolism
Recombinant Proteins
Repressor Proteins - chemistry
Repressor Proteins - genetics
Repressor Proteins - metabolism
title Type I Arginine Methyltransferases PRMT1 and PRMT-3 Act Distributively
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