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 |
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container_title | The Journal of biological chemistry |
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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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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.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M809547200</identifier><identifier>PMID: 19158082</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>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</subject><ispartof>The Journal of biological chemistry, 2009-03, Vol.284 (13), p.8274-8282</ispartof><rights>2009 © 2009 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>Copyright © 2009, The American Society for Biochemistry and Molecular Biology, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-3087f825a55216b82b55b26b7a6ae7b90ff39876f30200d932d1d62218345d073</citedby><cites>FETCH-LOGICAL-c489t-3087f825a55216b82b55b26b7a6ae7b90ff39876f30200d932d1d62218345d073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2659185/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2659185/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19158082$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kölbel, Knut</creatorcontrib><creatorcontrib>Ihling, Christian</creatorcontrib><creatorcontrib>Bellmann-Sickert, Kathrin</creatorcontrib><creatorcontrib>Neundorf, Ines</creatorcontrib><creatorcontrib>Beck-Sickinger, Annette G.</creatorcontrib><creatorcontrib>Sinz, Andrea</creatorcontrib><creatorcontrib>Kühn, Uwe</creatorcontrib><creatorcontrib>Wahle, Elmar</creatorcontrib><title>Type I Arginine Methyltransferases PRMT1 and PRMT-3 Act Distributively</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><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.</description><subject>Animals</subject><subject>Arginine - chemistry</subject><subject>Arginine - genetics</subject><subject>Arginine - metabolism</subject><subject>Humans</subject><subject>Methylation</subject><subject>Protein Processing, Post-Translational - physiology</subject><subject>Protein Synthesis, Post-Translational Modification, and Degradation</subject><subject>Protein-Arginine N-Methyltransferases - chemistry</subject><subject>Protein-Arginine N-Methyltransferases - genetics</subject><subject>Protein-Arginine N-Methyltransferases - metabolism</subject><subject>Recombinant Proteins</subject><subject>Repressor Proteins - chemistry</subject><subject>Repressor Proteins - genetics</subject><subject>Repressor Proteins - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1v0zAYhy3ExMrgyhEiIXFL8Uf8dUGqBoNJq0DQSdws23nTeEqTzk6L-t_jkWobh_liS3788-99EHpD8JxgWX28cX6-VFjzSlKMn6EZwYqVjJPfz9EMY0pKTbk6RS9TusF5VZq8QKdEE66wojN0sTpsobgsFnEd-tBDsYSxPXRjtH1qINoEqfjxc7kihe3rf6eSFQs_Fp9DGmNwuzHsoTu8QieN7RK8Pu5n6Priy-r8W3n1_evl-eKq9JXSY8mwko2i3HJOiXCKOs4dFU5aYUE6jZuGaSVFw3CeptaM1qQWlBLFKl5jyc7Qpyl3u3MbqD30uWlntjFsbDyYwQbz_00fWrMe9oYKroniOeDDMSAOtztIo9mE5KHrbA_DLhkhsyIhaAbnE-jjkFKE5v4Tgs2depPVmwf1-cHbx9Ue8KPrDLyfgDas2z8hgnFh8C1sDFWVIcwoKqtMvZuoxg7GrmNI5voXxYRhIrAi7G4ENRGQRe8DRJN8gN5DnTP9aOohPNXxL0eypWU</recordid><startdate>20090327</startdate><enddate>20090327</enddate><creator>Kölbel, Knut</creator><creator>Ihling, Christian</creator><creator>Bellmann-Sickert, Kathrin</creator><creator>Neundorf, Ines</creator><creator>Beck-Sickinger, Annette G.</creator><creator>Sinz, Andrea</creator><creator>Kühn, Uwe</creator><creator>Wahle, Elmar</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090327</creationdate><title>Type I Arginine Methyltransferases PRMT1 and PRMT-3 Act Distributively</title><author>Kölbel, Knut ; 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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. 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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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