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Linker region of nebulin family members plays an important role in targeting these molecules to cellular structures
The nebulin family of actin-binding proteins plays an essential role in cytoskeletal dynamics and actin filament stability. All of the family members are modular proteins with their key defining structural feature being the presence of the 35-residue nebulin modules. The family members now include n...
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Published in: | Cell and tissue research 2007-02, Vol.327 (2), p.353-369 |
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description | The nebulin family of actin-binding proteins plays an essential role in cytoskeletal dynamics and actin filament stability. All of the family members are modular proteins with their key defining structural feature being the presence of the 35-residue nebulin modules. The family members now include nebulin, nebulette, N-RAP, LASP-1, and LIM-nebulette. Nebulin and nebulette are associated with the thin filament/Z-line junction of striated muscle. LASP-1 and LIM-nebulette are found within focal adhesions, and N-RAP is associated with muscle cellular junctions. Although much investigation has focused on the role of the interactions between nebulin modules and actin, each of these proteins contains other domains that are essential for their cellular targeting and functions. The serine-rich linker region of nebulette has previously been shown to serve just such a purpose by targeting the association of the nebulin modules to the cardiac Z-line in cultured cardiomyocytes. In this report, we analyze the targeting functions of the homologous regions of LASP-1 and LIM-nebulette in their incorporation into focal adhesions. We have found that the linker region of LASP-1 is indeed important for its cellular localization and that the shortened linker region of LIM-nebulette drives the association of nebulin modules to focal adhesions. |
doi_str_mv | 10.1007/s00441-006-0305-2 |
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All of the family members are modular proteins with their key defining structural feature being the presence of the 35-residue nebulin modules. The family members now include nebulin, nebulette, N-RAP, LASP-1, and LIM-nebulette. Nebulin and nebulette are associated with the thin filament/Z-line junction of striated muscle. LASP-1 and LIM-nebulette are found within focal adhesions, and N-RAP is associated with muscle cellular junctions. Although much investigation has focused on the role of the interactions between nebulin modules and actin, each of these proteins contains other domains that are essential for their cellular targeting and functions. The serine-rich linker region of nebulette has previously been shown to serve just such a purpose by targeting the association of the nebulin modules to the cardiac Z-line in cultured cardiomyocytes. In this report, we analyze the targeting functions of the homologous regions of LASP-1 and LIM-nebulette in their incorporation into focal adhesions. We have found that the linker region of LASP-1 is indeed important for its cellular localization and that the shortened linker region of LIM-nebulette drives the association of nebulin modules to focal adhesions.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/s00441-006-0305-2</identifier><identifier>PMID: 17177073</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Actinin - analysis ; Amino Acid Sequence ; Animals ; Carrier Proteins - analysis ; Carrier Proteins - genetics ; Carrier Proteins - metabolism ; Cell adhesion & migration ; Cell Line ; Cells, Cultured ; Cercopithecus aethiops ; Chick Embryo ; COS Cells ; Cytoskeletal Proteins - analysis ; Cytoskeletal Proteins - genetics ; Cytoskeletal Proteins - metabolism ; Cytoskeleton ; Epithelial Cells - chemistry ; Epithelial Cells - metabolism ; Green Fluorescent Proteins - genetics ; Green Fluorescent Proteins - metabolism ; Humans ; LIM Domain Proteins ; Mice ; Microfilament Proteins - analysis ; Microfilament Proteins - genetics ; Microfilament Proteins - metabolism ; Microscopy, Fluorescence ; Molecular Sequence Data ; Muscle Proteins - analysis ; Muscle Proteins - genetics ; Muscle Proteins - metabolism ; Muscular system ; Myocytes, Cardiac - chemistry ; Myocytes, Cardiac - metabolism ; Peptide Fragments - analysis ; Peptide Fragments - genetics ; Peptide Fragments - metabolism ; Potoroidae ; Protein Transport ; Proteins ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - metabolism ; Sequence Homology, Amino Acid ; Transfection</subject><ispartof>Cell and tissue research, 2007-02, Vol.327 (2), p.353-369</ispartof><rights>Springer-Verlag 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c326t-f0fd8b6b473691cb9b8304eb8de3213bde103efb2c3fb010c5db85ff8350fbc93</citedby><cites>FETCH-LOGICAL-c326t-f0fd8b6b473691cb9b8304eb8de3213bde103efb2c3fb010c5db85ff8350fbc93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17177073$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Panaviene, Zivile</creatorcontrib><creatorcontrib>Moncman, Carole L</creatorcontrib><title>Linker region of nebulin family members plays an important role in targeting these molecules to cellular structures</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><description>The nebulin family of actin-binding proteins plays an essential role in cytoskeletal dynamics and actin filament stability. All of the family members are modular proteins with their key defining structural feature being the presence of the 35-residue nebulin modules. The family members now include nebulin, nebulette, N-RAP, LASP-1, and LIM-nebulette. Nebulin and nebulette are associated with the thin filament/Z-line junction of striated muscle. LASP-1 and LIM-nebulette are found within focal adhesions, and N-RAP is associated with muscle cellular junctions. Although much investigation has focused on the role of the interactions between nebulin modules and actin, each of these proteins contains other domains that are essential for their cellular targeting and functions. The serine-rich linker region of nebulette has previously been shown to serve just such a purpose by targeting the association of the nebulin modules to the cardiac Z-line in cultured cardiomyocytes. In this report, we analyze the targeting functions of the homologous regions of LASP-1 and LIM-nebulette in their incorporation into focal adhesions. We have found that the linker region of LASP-1 is indeed important for its cellular localization and that the shortened linker region of LIM-nebulette drives the association of nebulin modules to focal adhesions.</description><subject>Actinin - analysis</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Carrier Proteins - analysis</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - metabolism</subject><subject>Cell adhesion & migration</subject><subject>Cell Line</subject><subject>Cells, Cultured</subject><subject>Cercopithecus aethiops</subject><subject>Chick Embryo</subject><subject>COS Cells</subject><subject>Cytoskeletal Proteins - analysis</subject><subject>Cytoskeletal Proteins - genetics</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Cytoskeleton</subject><subject>Epithelial Cells - chemistry</subject><subject>Epithelial Cells - metabolism</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Humans</subject><subject>LIM Domain Proteins</subject><subject>Mice</subject><subject>Microfilament Proteins - analysis</subject><subject>Microfilament Proteins - genetics</subject><subject>Microfilament Proteins - metabolism</subject><subject>Microscopy, Fluorescence</subject><subject>Molecular Sequence Data</subject><subject>Muscle Proteins - analysis</subject><subject>Muscle Proteins - genetics</subject><subject>Muscle Proteins - metabolism</subject><subject>Muscular system</subject><subject>Myocytes, Cardiac - chemistry</subject><subject>Myocytes, Cardiac - metabolism</subject><subject>Peptide Fragments - analysis</subject><subject>Peptide Fragments - genetics</subject><subject>Peptide Fragments - metabolism</subject><subject>Potoroidae</subject><subject>Protein Transport</subject><subject>Proteins</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Sequence Homology, Amino Acid</subject><subject>Transfection</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNpdkU9r3DAQxUVpaTZpP0AvRfSQm9uRZcvysYSkKSz00kBuQpJHW6eytNWfw3772uxCoaeBx2_ePOYR8oHBZwYwfMkAXccaANEAh75pX5Ed63jbgBzka7JbxbYZhHi-Itc5vwCwTojxLbliAxsGGPiO5P0cfmOiCQ9zDDQ6GtBUPwfq9DL7E11wMZgyPXp9ylQHOi_HmIoOhaboka5k0emAZQ4HWn5hRrqsuq0eMy2RWvS-ep1oLqnaUhPmd-SN0z7j-8u8IU8P9z_vHpv9j2_f777uG8tbURoHbpJGmG7gYmTWjEZy6NDICXnLuJmQAUdnWsudAQa2n4zsnZO8B2fsyG_I7dn3mOKfirmoZc5bHh0w1qyE5CNI3q7gp__Al1hTWLOp9dDQMzluEDtDNsWcEzp1TPOi00kxUFsd6lyHWutQWx1q2_l4Ma5mwenfxuX__C-J0ogO</recordid><startdate>20070201</startdate><enddate>20070201</enddate><creator>Panaviene, Zivile</creator><creator>Moncman, Carole L</creator><general>Springer Nature B.V</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>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SS</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20070201</creationdate><title>Linker region of nebulin family members plays an important role in targeting these molecules to cellular structures</title><author>Panaviene, Zivile ; Moncman, Carole L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-f0fd8b6b473691cb9b8304eb8de3213bde103efb2c3fb010c5db85ff8350fbc93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Actinin - 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analysis</topic><topic>Muscle Proteins - genetics</topic><topic>Muscle Proteins - metabolism</topic><topic>Muscular system</topic><topic>Myocytes, Cardiac - chemistry</topic><topic>Myocytes, Cardiac - metabolism</topic><topic>Peptide Fragments - analysis</topic><topic>Peptide Fragments - genetics</topic><topic>Peptide Fragments - metabolism</topic><topic>Potoroidae</topic><topic>Protein Transport</topic><topic>Proteins</topic><topic>Recombinant Fusion Proteins - genetics</topic><topic>Recombinant Fusion Proteins - metabolism</topic><topic>Sequence Homology, Amino Acid</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Panaviene, Zivile</creatorcontrib><creatorcontrib>Moncman, Carole L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Panaviene, Zivile</au><au>Moncman, Carole L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Linker region of nebulin family members plays an important role in targeting these molecules to cellular structures</atitle><jtitle>Cell and tissue research</jtitle><addtitle>Cell Tissue Res</addtitle><date>2007-02-01</date><risdate>2007</risdate><volume>327</volume><issue>2</issue><spage>353</spage><epage>369</epage><pages>353-369</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><abstract>The nebulin family of actin-binding proteins plays an essential role in cytoskeletal dynamics and actin filament stability. All of the family members are modular proteins with their key defining structural feature being the presence of the 35-residue nebulin modules. The family members now include nebulin, nebulette, N-RAP, LASP-1, and LIM-nebulette. Nebulin and nebulette are associated with the thin filament/Z-line junction of striated muscle. LASP-1 and LIM-nebulette are found within focal adhesions, and N-RAP is associated with muscle cellular junctions. Although much investigation has focused on the role of the interactions between nebulin modules and actin, each of these proteins contains other domains that are essential for their cellular targeting and functions. The serine-rich linker region of nebulette has previously been shown to serve just such a purpose by targeting the association of the nebulin modules to the cardiac Z-line in cultured cardiomyocytes. In this report, we analyze the targeting functions of the homologous regions of LASP-1 and LIM-nebulette in their incorporation into focal adhesions. We have found that the linker region of LASP-1 is indeed important for its cellular localization and that the shortened linker region of LIM-nebulette drives the association of nebulin modules to focal adhesions.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>17177073</pmid><doi>10.1007/s00441-006-0305-2</doi><tpages>17</tpages></addata></record> |
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subjects | Actinin - analysis Amino Acid Sequence Animals Carrier Proteins - analysis Carrier Proteins - genetics Carrier Proteins - metabolism Cell adhesion & migration Cell Line Cells, Cultured Cercopithecus aethiops Chick Embryo COS Cells Cytoskeletal Proteins - analysis Cytoskeletal Proteins - genetics Cytoskeletal Proteins - metabolism Cytoskeleton Epithelial Cells - chemistry Epithelial Cells - metabolism Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism Humans LIM Domain Proteins Mice Microfilament Proteins - analysis Microfilament Proteins - genetics Microfilament Proteins - metabolism Microscopy, Fluorescence Molecular Sequence Data Muscle Proteins - analysis Muscle Proteins - genetics Muscle Proteins - metabolism Muscular system Myocytes, Cardiac - chemistry Myocytes, Cardiac - metabolism Peptide Fragments - analysis Peptide Fragments - genetics Peptide Fragments - metabolism Potoroidae Protein Transport Proteins Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - metabolism Sequence Homology, Amino Acid Transfection |
title | Linker region of nebulin family members plays an important role in targeting these molecules to cellular structures |
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