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Pyrrolizidine Alkaloids Crosslink DNA with Actin

Pyrrolizidine alkaloids (PAs) are toxic constituents of hundreds of plant species, some of which people are exposed to in herbal products and traditional remedies. The bioactivity of PAs are related, at least in part, to their ability to form DNA–protein complexes (DPC). Previous studies from our la...

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Published in:Toxicology and applied pharmacology 1999-01, Vol.154 (2), p.198-202
Main Authors: Coulombe, Roger A., Drew, Gail L., Stermitz, Frank R.
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description Pyrrolizidine alkaloids (PAs) are toxic constituents of hundreds of plant species, some of which people are exposed to in herbal products and traditional remedies. The bioactivity of PAs are related, at least in part, to their ability to form DNA–protein complexes (DPC). Previous studies from our laboratory indicated a possible role for actin in PA-induced DPCs. Nuclei prepared from Madin-Darby bovine kidney (MDBK) and human breast carcinoma (MCF-7) cells were treated with the pyrrolic PAs dehydrosenecionine (DHSN) and dehydromonocrotaline (DHMO). DPCs were purified and then analyzed by Western immunoblotting. Actin was found in DPCs induced by both DHSN and DHMO, but not in those from control nuclei. Actin was also present in DPCs induced by cisplatinum and mitomycin C, two bifunctional cross-linkers. In separate experiments, DHSN and DHMO were crosslinked to a mixture ofHindIII digested λ phage with varying amounts of glutathione (GSH), cysteine, or methionine to identify the stoichiometry of competition between DNA and alternate nucleophiles for crosslink formation with pyrroles. GSH and cysteine, but not methionine, competed with λ phage for DNA crosslinking, indicating that reduced thiols may have a role in nucleophilic reactions with pyrroles in the cell. While actin involvement in cisplatinum-induced DPCs is documented, the discovery of actin crosslinking in PA or mitomycin C-treated cells or nuclei is, to our knowledge, novel. Pyrrole-induced DPC formation with actin, a protein with structural and/or regulatory importance proteins, may be a significant mechanism for PA toxicity and bioactivity.
doi_str_mv 10.1006/taap.1998.8552
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The bioactivity of PAs are related, at least in part, to their ability to form DNA–protein complexes (DPC). Previous studies from our laboratory indicated a possible role for actin in PA-induced DPCs. Nuclei prepared from Madin-Darby bovine kidney (MDBK) and human breast carcinoma (MCF-7) cells were treated with the pyrrolic PAs dehydrosenecionine (DHSN) and dehydromonocrotaline (DHMO). DPCs were purified and then analyzed by Western immunoblotting. Actin was found in DPCs induced by both DHSN and DHMO, but not in those from control nuclei. Actin was also present in DPCs induced by cisplatinum and mitomycin C, two bifunctional cross-linkers. In separate experiments, DHSN and DHMO were crosslinked to a mixture ofHindIII digested λ phage with varying amounts of glutathione (GSH), cysteine, or methionine to identify the stoichiometry of competition between DNA and alternate nucleophiles for crosslink formation with pyrroles. GSH and cysteine, but not methionine, competed with λ phage for DNA crosslinking, indicating that reduced thiols may have a role in nucleophilic reactions with pyrroles in the cell. While actin involvement in cisplatinum-induced DPCs is documented, the discovery of actin crosslinking in PA or mitomycin C-treated cells or nuclei is, to our knowledge, novel. 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The bioactivity of PAs are related, at least in part, to their ability to form DNA–protein complexes (DPC). Previous studies from our laboratory indicated a possible role for actin in PA-induced DPCs. Nuclei prepared from Madin-Darby bovine kidney (MDBK) and human breast carcinoma (MCF-7) cells were treated with the pyrrolic PAs dehydrosenecionine (DHSN) and dehydromonocrotaline (DHMO). DPCs were purified and then analyzed by Western immunoblotting. Actin was found in DPCs induced by both DHSN and DHMO, but not in those from control nuclei. Actin was also present in DPCs induced by cisplatinum and mitomycin C, two bifunctional cross-linkers. In separate experiments, DHSN and DHMO were crosslinked to a mixture ofHindIII digested λ phage with varying amounts of glutathione (GSH), cysteine, or methionine to identify the stoichiometry of competition between DNA and alternate nucleophiles for crosslink formation with pyrroles. GSH and cysteine, but not methionine, competed with λ phage for DNA crosslinking, indicating that reduced thiols may have a role in nucleophilic reactions with pyrroles in the cell. While actin involvement in cisplatinum-induced DPCs is documented, the discovery of actin crosslinking in PA or mitomycin C-treated cells or nuclei is, to our knowledge, novel. Pyrrole-induced DPC formation with actin, a protein with structural and/or regulatory importance proteins, may be a significant mechanism for PA toxicity and bioactivity.</description><subject>actin</subject><subject>Actins - chemistry</subject><subject>Animals</subject><subject>Bacteriophage lambda - metabolism</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Carcinogenesis, carcinogens and anticarcinogens</subject><subject>Carcinogens - chemistry</subject><subject>Cattle</subject><subject>Cell Line</subject><subject>Chemical agents</subject><subject>chemical reactions</subject><subject>Cross-Linking Reagents</subject><subject>DNA</subject><subject>dna crosslinking</subject><subject>dna modification</subject><subject>dna protein complexes</subject><subject>DNA, Viral - chemistry</subject><subject>genotoxicity</subject><subject>Humans</subject><subject>Hydrogen-Ion Concentration</subject><subject>Indicators and Reagents</subject><subject>Medical sciences</subject><subject>pyrrolizidine alkaloids</subject><subject>Pyrrolizidine Alkaloids - chemistry</subject><subject>Senecio vulgaris</subject><subject>senecionine</subject><subject>Tumors</subject><issn>0041-008X</issn><issn>1096-0333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLxDAUhYMoOj627sQuxF3Hm6RNk-UwPkFUUMFdSJNbjXbaMeko-uttmUFXru7ifPdw-AjZpzCmAOKkM2Y-pkrJscxztkZGFJRIgXO-TkYAGU0B5NMW2Y7xFQBUltFNsqkUyyVkIwJ3XyG0tf_2zjeYTOo3U7fexWQa2hhr37wlpzeT5NN3L8nEdr7ZJRuVqSPure4OeTw_e5hepte3F1fTyXVqM8a7tMwctyCoUSgcWsaqKjdOWWHQFMyUzEHRj-GVYoy5zBaiLNFBbrHEokTGd8jxsnce2vcFxk7PfLRY16bBdhE1lRktZE57cLwE7bA4YKXnwc9M-NIU9KBID4r0oEgPivqHg1Xzopyh-8VXTvr8aJWbaE1dBdNYH_9ahZQgeI8dLrHKtNo8hx55vGdAOTCpBDDVE3JJYO_pw2PQ0XpsLDof0Hbatf6_jT9upYtL</recordid><startdate>19990115</startdate><enddate>19990115</enddate><creator>Coulombe, Roger A.</creator><creator>Drew, Gail L.</creator><creator>Stermitz, Frank R.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>19990115</creationdate><title>Pyrrolizidine Alkaloids Crosslink DNA with Actin</title><author>Coulombe, Roger A. ; Drew, Gail L. ; Stermitz, Frank R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-b4d3c061a9e6dec22ff5ad9c6aea72ab2d070943f9222d4c76bbed05cebe7be23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>actin</topic><topic>Actins - chemistry</topic><topic>Animals</topic><topic>Bacteriophage lambda - metabolism</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Carcinogenesis, carcinogens and anticarcinogens</topic><topic>Carcinogens - chemistry</topic><topic>Cattle</topic><topic>Cell Line</topic><topic>Chemical agents</topic><topic>chemical reactions</topic><topic>Cross-Linking Reagents</topic><topic>DNA</topic><topic>dna crosslinking</topic><topic>dna modification</topic><topic>dna protein complexes</topic><topic>DNA, Viral - chemistry</topic><topic>genotoxicity</topic><topic>Humans</topic><topic>Hydrogen-Ion Concentration</topic><topic>Indicators and Reagents</topic><topic>Medical sciences</topic><topic>pyrrolizidine alkaloids</topic><topic>Pyrrolizidine Alkaloids - chemistry</topic><topic>Senecio vulgaris</topic><topic>senecionine</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Coulombe, Roger A.</creatorcontrib><creatorcontrib>Drew, Gail L.</creatorcontrib><creatorcontrib>Stermitz, Frank R.</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicology and applied pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Coulombe, Roger A.</au><au>Drew, Gail L.</au><au>Stermitz, Frank R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pyrrolizidine Alkaloids Crosslink DNA with Actin</atitle><jtitle>Toxicology and applied pharmacology</jtitle><addtitle>Toxicol Appl Pharmacol</addtitle><date>1999-01-15</date><risdate>1999</risdate><volume>154</volume><issue>2</issue><spage>198</spage><epage>202</epage><pages>198-202</pages><issn>0041-008X</issn><eissn>1096-0333</eissn><coden>TXAPA9</coden><abstract>Pyrrolizidine alkaloids (PAs) are toxic constituents of hundreds of plant species, some of which people are exposed to in herbal products and traditional remedies. The bioactivity of PAs are related, at least in part, to their ability to form DNA–protein complexes (DPC). Previous studies from our laboratory indicated a possible role for actin in PA-induced DPCs. Nuclei prepared from Madin-Darby bovine kidney (MDBK) and human breast carcinoma (MCF-7) cells were treated with the pyrrolic PAs dehydrosenecionine (DHSN) and dehydromonocrotaline (DHMO). DPCs were purified and then analyzed by Western immunoblotting. Actin was found in DPCs induced by both DHSN and DHMO, but not in those from control nuclei. Actin was also present in DPCs induced by cisplatinum and mitomycin C, two bifunctional cross-linkers. In separate experiments, DHSN and DHMO were crosslinked to a mixture ofHindIII digested λ phage with varying amounts of glutathione (GSH), cysteine, or methionine to identify the stoichiometry of competition between DNA and alternate nucleophiles for crosslink formation with pyrroles. GSH and cysteine, but not methionine, competed with λ phage for DNA crosslinking, indicating that reduced thiols may have a role in nucleophilic reactions with pyrroles in the cell. While actin involvement in cisplatinum-induced DPCs is documented, the discovery of actin crosslinking in PA or mitomycin C-treated cells or nuclei is, to our knowledge, novel. Pyrrole-induced DPC formation with actin, a protein with structural and/or regulatory importance proteins, may be a significant mechanism for PA toxicity and bioactivity.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>9925804</pmid><doi>10.1006/taap.1998.8552</doi><tpages>5</tpages></addata></record>
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1096-0333
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subjects actin
Actins - chemistry
Animals
Bacteriophage lambda - metabolism
Biological and medical sciences
Blotting, Western
Carcinogenesis, carcinogens and anticarcinogens
Carcinogens - chemistry
Cattle
Cell Line
Chemical agents
chemical reactions
Cross-Linking Reagents
DNA
dna crosslinking
dna modification
dna protein complexes
DNA, Viral - chemistry
genotoxicity
Humans
Hydrogen-Ion Concentration
Indicators and Reagents
Medical sciences
pyrrolizidine alkaloids
Pyrrolizidine Alkaloids - chemistry
Senecio vulgaris
senecionine
Tumors
title Pyrrolizidine Alkaloids Crosslink DNA with Actin
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