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Long-Range Effects of Familial Hypertrophic Cardiomyopathy Mutations E180G and D175N on the Properties of Tropomyosin
Cardiac α-tropomyosin (Tm) single-site mutations D175N and E180G cause familial hypertrophic cardiomyopathy (FHC). Previous studies have shown that these mutations increase both Ca2+ sensitivity and residual contractile activity at low Ca2+ concentrations, which causes incomplete relaxation during d...
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Published in: | Biochemistry (Easton) 2012-08, Vol.51 (32), p.6413-6420 |
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description | Cardiac α-tropomyosin (Tm) single-site mutations D175N and E180G cause familial hypertrophic cardiomyopathy (FHC). Previous studies have shown that these mutations increase both Ca2+ sensitivity and residual contractile activity at low Ca2+ concentrations, which causes incomplete relaxation during diastole resulting in hypertrophy and sarcomeric disarray. However, the molecular basis for the cause and the difference in the severity of the manifested phenotypes of disease are not known. In this work we have (1) used ATPase studies using reconstituted thin filaments in solution to show that these FHC mutants result in an increase in Ca2+ sensitivity and an increased residual level of ATPase, (2) shown that both FHC mutants increase the rate of cleavage at R133, ∼45 residues N-terminal to the mutations, when free and bound to actin, (3) shown that for Tm-E180G, the increase in the rate of cleavage is greater than that for D175N, and (4) shown that for E180G, cleavage also occurs at a new site 53 residues C-terminal to E180G, in parallel with cleavage at R133. The long-range decreases in dynamic stability due to these two single-site mutations suggest increases in flexibility that may weaken the ability of Tm to inhibit activity at low Ca2+ concentrations for D175N and to a greater degree for E180G, which may contribute to differences in the severity of FHC. |
doi_str_mv | 10.1021/bi3006835 |
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Previous studies have shown that these mutations increase both Ca2+ sensitivity and residual contractile activity at low Ca2+ concentrations, which causes incomplete relaxation during diastole resulting in hypertrophy and sarcomeric disarray. However, the molecular basis for the cause and the difference in the severity of the manifested phenotypes of disease are not known. In this work we have (1) used ATPase studies using reconstituted thin filaments in solution to show that these FHC mutants result in an increase in Ca2+ sensitivity and an increased residual level of ATPase, (2) shown that both FHC mutants increase the rate of cleavage at R133, ∼45 residues N-terminal to the mutations, when free and bound to actin, (3) shown that for Tm-E180G, the increase in the rate of cleavage is greater than that for D175N, and (4) shown that for E180G, cleavage also occurs at a new site 53 residues C-terminal to E180G, in parallel with cleavage at R133. The long-range decreases in dynamic stability due to these two single-site mutations suggest increases in flexibility that may weaken the ability of Tm to inhibit activity at low Ca2+ concentrations for D175N and to a greater degree for E180G, which may contribute to differences in the severity of FHC.</description><identifier>ISSN: 0006-2960</identifier><identifier>EISSN: 1520-4995</identifier><identifier>DOI: 10.1021/bi3006835</identifier><identifier>PMID: 22794249</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Actins - chemistry ; Adenosine Triphosphatases - chemistry ; Amino Acid Substitution ; Animals ; Calcium Chloride - chemistry ; Cardiomyopathy, Hypertrophic, Familial - genetics ; Cations, Divalent ; Hot Temperature ; Humans ; Mutation ; Protein Stability ; Protein Unfolding ; Rabbits ; Rats ; Recombinant Proteins - chemistry ; Recombinant Proteins - genetics ; Tropomyosin - chemistry ; Tropomyosin - genetics ; Trypsin - chemistry</subject><ispartof>Biochemistry (Easton), 2012-08, Vol.51 (32), p.6413-6420</ispartof><rights>Copyright © 2012 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a405t-51f4e2f2403895f48d096c83b4b86b026e4f42caf948a6538d32b125d1d198903</citedby><cites>FETCH-LOGICAL-a405t-51f4e2f2403895f48d096c83b4b86b026e4f42caf948a6538d32b125d1d198903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22794249$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ly, Socheata</creatorcontrib><creatorcontrib>Lehrer, Sherwin S</creatorcontrib><title>Long-Range Effects of Familial Hypertrophic Cardiomyopathy Mutations E180G and D175N on the Properties of Tropomyosin</title><title>Biochemistry (Easton)</title><addtitle>Biochemistry</addtitle><description>Cardiac α-tropomyosin (Tm) single-site mutations D175N and E180G cause familial hypertrophic cardiomyopathy (FHC). Previous studies have shown that these mutations increase both Ca2+ sensitivity and residual contractile activity at low Ca2+ concentrations, which causes incomplete relaxation during diastole resulting in hypertrophy and sarcomeric disarray. However, the molecular basis for the cause and the difference in the severity of the manifested phenotypes of disease are not known. In this work we have (1) used ATPase studies using reconstituted thin filaments in solution to show that these FHC mutants result in an increase in Ca2+ sensitivity and an increased residual level of ATPase, (2) shown that both FHC mutants increase the rate of cleavage at R133, ∼45 residues N-terminal to the mutations, when free and bound to actin, (3) shown that for Tm-E180G, the increase in the rate of cleavage is greater than that for D175N, and (4) shown that for E180G, cleavage also occurs at a new site 53 residues C-terminal to E180G, in parallel with cleavage at R133. The long-range decreases in dynamic stability due to these two single-site mutations suggest increases in flexibility that may weaken the ability of Tm to inhibit activity at low Ca2+ concentrations for D175N and to a greater degree for E180G, which may contribute to differences in the severity of FHC.</description><subject>Actins - chemistry</subject><subject>Adenosine Triphosphatases - chemistry</subject><subject>Amino Acid Substitution</subject><subject>Animals</subject><subject>Calcium Chloride - chemistry</subject><subject>Cardiomyopathy, Hypertrophic, Familial - genetics</subject><subject>Cations, Divalent</subject><subject>Hot Temperature</subject><subject>Humans</subject><subject>Mutation</subject><subject>Protein Stability</subject><subject>Protein Unfolding</subject><subject>Rabbits</subject><subject>Rats</subject><subject>Recombinant Proteins - chemistry</subject><subject>Recombinant Proteins - genetics</subject><subject>Tropomyosin - chemistry</subject><subject>Tropomyosin - genetics</subject><subject>Trypsin - chemistry</subject><issn>0006-2960</issn><issn>1520-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNptkE1LAzEQhoMotlYP_gHJxYOH1SSbbJOLILUfQv1A6nnJ7ibdSJssyVbYf29qtSh4GmbmfZ9hXgDOMbrGiOCbwqQIZTxlB6CPGUEJFYIdgj6K04SIDPXASQjvsaVoSI9Bj5ChoISKPtjMnV0mr9IuFRxrrco2QKfhRK7NysgVnHWN8q13TW1KOJK-Mm7duUa2dQcfN61sjbMBjjFHUyhtBe_xkD1BZ2FbK_gSfdFt1BdzEbutORh7Co60XAV19l0H4G0yXoxmyfx5-jC6myeSItYmDGuqiCYUpVwwTXmFRFbytKAFzwpEMkU1JaXUgnKZsZRXKSkwYRWusOACpQNwu-M2m2KtqlLZ1stV3nizlr7LnTT53401db50H3lK6VAIEgFXO0DpXQhe6b0Xo3ybfb7PPmovfh_bK3_CjoLLnUCWIX93G2_j7_-APgEnZIsc</recordid><startdate>20120814</startdate><enddate>20120814</enddate><creator>Ly, Socheata</creator><creator>Lehrer, Sherwin S</creator><general>American Chemical Society</general><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>5PM</scope></search><sort><creationdate>20120814</creationdate><title>Long-Range Effects of Familial Hypertrophic Cardiomyopathy Mutations E180G and D175N on the Properties of Tropomyosin</title><author>Ly, Socheata ; Lehrer, Sherwin S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a405t-51f4e2f2403895f48d096c83b4b86b026e4f42caf948a6538d32b125d1d198903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Actins - chemistry</topic><topic>Adenosine Triphosphatases - chemistry</topic><topic>Amino Acid Substitution</topic><topic>Animals</topic><topic>Calcium Chloride - chemistry</topic><topic>Cardiomyopathy, Hypertrophic, Familial - genetics</topic><topic>Cations, Divalent</topic><topic>Hot Temperature</topic><topic>Humans</topic><topic>Mutation</topic><topic>Protein Stability</topic><topic>Protein Unfolding</topic><topic>Rabbits</topic><topic>Rats</topic><topic>Recombinant Proteins - chemistry</topic><topic>Recombinant Proteins - genetics</topic><topic>Tropomyosin - chemistry</topic><topic>Tropomyosin - genetics</topic><topic>Trypsin - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ly, Socheata</creatorcontrib><creatorcontrib>Lehrer, Sherwin S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochemistry (Easton)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ly, Socheata</au><au>Lehrer, Sherwin S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-Range Effects of Familial Hypertrophic Cardiomyopathy Mutations E180G and D175N on the Properties of Tropomyosin</atitle><jtitle>Biochemistry (Easton)</jtitle><addtitle>Biochemistry</addtitle><date>2012-08-14</date><risdate>2012</risdate><volume>51</volume><issue>32</issue><spage>6413</spage><epage>6420</epage><pages>6413-6420</pages><issn>0006-2960</issn><eissn>1520-4995</eissn><abstract>Cardiac α-tropomyosin (Tm) single-site mutations D175N and E180G cause familial hypertrophic cardiomyopathy (FHC). Previous studies have shown that these mutations increase both Ca2+ sensitivity and residual contractile activity at low Ca2+ concentrations, which causes incomplete relaxation during diastole resulting in hypertrophy and sarcomeric disarray. However, the molecular basis for the cause and the difference in the severity of the manifested phenotypes of disease are not known. In this work we have (1) used ATPase studies using reconstituted thin filaments in solution to show that these FHC mutants result in an increase in Ca2+ sensitivity and an increased residual level of ATPase, (2) shown that both FHC mutants increase the rate of cleavage at R133, ∼45 residues N-terminal to the mutations, when free and bound to actin, (3) shown that for Tm-E180G, the increase in the rate of cleavage is greater than that for D175N, and (4) shown that for E180G, cleavage also occurs at a new site 53 residues C-terminal to E180G, in parallel with cleavage at R133. The long-range decreases in dynamic stability due to these two single-site mutations suggest increases in flexibility that may weaken the ability of Tm to inhibit activity at low Ca2+ concentrations for D175N and to a greater degree for E180G, which may contribute to differences in the severity of FHC.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>22794249</pmid><doi>10.1021/bi3006835</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actins - chemistry Adenosine Triphosphatases - chemistry Amino Acid Substitution Animals Calcium Chloride - chemistry Cardiomyopathy, Hypertrophic, Familial - genetics Cations, Divalent Hot Temperature Humans Mutation Protein Stability Protein Unfolding Rabbits Rats Recombinant Proteins - chemistry Recombinant Proteins - genetics Tropomyosin - chemistry Tropomyosin - genetics Trypsin - chemistry |
title | Long-Range Effects of Familial Hypertrophic Cardiomyopathy Mutations E180G and D175N on the Properties of Tropomyosin |
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