Mandibular muscle troponin of the Florida carpenter ant Camponotus floridanus: extending our insights into invertebrate Ca2+ regulation
Ants use their mandibles for a variety of functions and behaviors. We investigated mandibular muscle structure and function from major workers of the Florida carpenter ant Camponotus floridanus : force-pCa relation and velocity of unloaded shortening of single, permeabilized fibres, primary sequence...
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Veröffentlicht in: | Journal of muscle research and cell motility 2021-06, Vol.42 (2), p.399-417 |
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creator | Shi, Yun Bethea, Julia P. Hetzel-Ebben, Hannah L. Landim-Vieira, Maicon Mayper, Ross J. Williams, Regan L. Kessler, Lauren E. Ruiz, Amanda M. Gargiulo, Kathryn Rose, Jennifer S. M. Platt, Grayson Pinto, Jose R. Washburn, Brian K. Chase, P. Bryant |
description | Ants use their mandibles for a variety of functions and behaviors. We investigated mandibular muscle structure and function from major workers of the Florida carpenter ant
Camponotus floridanus
: force-pCa relation and velocity of unloaded shortening of single, permeabilized fibres, primary sequences of troponin subunits (TnC, TnI and TnT) from a mandibular muscle cDNA library, and muscle fibre ultrastructure. From the mechanical measurements, we found Ca
2+
-sensitivity of isometric force was markedly shifted rightward compared with vertebrate striated muscle. From the troponin sequence results, we identified features that could explain the rightward shift of Ca
2+
-activation: the N-helix of TnC is effectively absent and three of the four EF-hands of TnC (sites I, II and III) do not adhere to canonical sequence rules for divalent cation binding; two alternatively spliced isoforms of TnI were identified with the alternatively spliced exon occurring in the region of the IT-arm α-helical coiled-coil, and the N-terminal extension of TnI may be involved in modulation of regulation, as in mammalian cardiac muscle; and TnT has a Glu-rich C-terminus. In addition, a structural homology model was built of
C. floridanus
troponin on the thin filament. From analysis of electron micrographs, we found thick filaments are almost as long as the 6.8 μm sarcomeres, have diameter of ~ 16 nm, and typical center-to-center spacing of ~ 46 nm. These results have implications for the mechanisms by which mandibular muscle fibres perform such a variety of functions, and how the structure of the troponin complex aids in these tasks. |
doi_str_mv | 10.1007/s10974-021-09606-w |
format | Article |
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Camponotus floridanus
: force-pCa relation and velocity of unloaded shortening of single, permeabilized fibres, primary sequences of troponin subunits (TnC, TnI and TnT) from a mandibular muscle cDNA library, and muscle fibre ultrastructure. From the mechanical measurements, we found Ca
2+
-sensitivity of isometric force was markedly shifted rightward compared with vertebrate striated muscle. From the troponin sequence results, we identified features that could explain the rightward shift of Ca
2+
-activation: the N-helix of TnC is effectively absent and three of the four EF-hands of TnC (sites I, II and III) do not adhere to canonical sequence rules for divalent cation binding; two alternatively spliced isoforms of TnI were identified with the alternatively spliced exon occurring in the region of the IT-arm α-helical coiled-coil, and the N-terminal extension of TnI may be involved in modulation of regulation, as in mammalian cardiac muscle; and TnT has a Glu-rich C-terminus. In addition, a structural homology model was built of
C. floridanus
troponin on the thin filament. From analysis of electron micrographs, we found thick filaments are almost as long as the 6.8 μm sarcomeres, have diameter of ~ 16 nm, and typical center-to-center spacing of ~ 46 nm. These results have implications for the mechanisms by which mandibular muscle fibres perform such a variety of functions, and how the structure of the troponin complex aids in these tasks.</description><identifier>ISSN: 0142-4319</identifier><identifier>EISSN: 1573-2657</identifier><identifier>DOI: 10.1007/s10974-021-09606-w</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Alternative splicing ; Animal Anatomy ; Biomedical and Life Sciences ; Biomedicine ; C-Terminus ; Calcium-binding protein ; Camponotus floridanus ; Cardiac muscle ; Cell Biology ; Filaments ; Glycerol ; Histology ; Homology ; Invertebrates ; Isoforms ; Life Sciences ; Mandible ; Mechanics ; Morphology ; Motility ; Muscle contraction ; Proteomics ; Sarcomeres ; Skeletal muscle ; Structure-function relationships ; Troponin ; Ultrastructure ; Workers (insect caste)</subject><ispartof>Journal of muscle research and cell motility, 2021-06, Vol.42 (2), p.399-417</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Switzerland AG 2021</rights><rights>The Author(s), under exclusive licence to Springer Nature Switzerland AG 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c282t-d601a4dc9921c81c6b663e1f160192886066357150ecfcefc0786098bfd798573</citedby><cites>FETCH-LOGICAL-c282t-d601a4dc9921c81c6b663e1f160192886066357150ecfcefc0786098bfd798573</cites><orcidid>0000-0003-0405-2062 ; 0000-0002-4279-7770 ; 0000-0002-2970-2458 ; 0000-0002-6696-8888 ; 0000-0003-0738-6658 ; 0000-0002-7725-467X ; 0000-0003-2460-6691 ; 0000-0001-9701-561X ; 0000-0002-8662-3983 ; 0000-0001-9092-4976 ; 0000-0002-8844-0099</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10974-021-09606-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10974-021-09606-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Shi, Yun</creatorcontrib><creatorcontrib>Bethea, Julia P.</creatorcontrib><creatorcontrib>Hetzel-Ebben, Hannah L.</creatorcontrib><creatorcontrib>Landim-Vieira, Maicon</creatorcontrib><creatorcontrib>Mayper, Ross J.</creatorcontrib><creatorcontrib>Williams, Regan L.</creatorcontrib><creatorcontrib>Kessler, Lauren E.</creatorcontrib><creatorcontrib>Ruiz, Amanda M.</creatorcontrib><creatorcontrib>Gargiulo, Kathryn</creatorcontrib><creatorcontrib>Rose, Jennifer S. M.</creatorcontrib><creatorcontrib>Platt, Grayson</creatorcontrib><creatorcontrib>Pinto, Jose R.</creatorcontrib><creatorcontrib>Washburn, Brian K.</creatorcontrib><creatorcontrib>Chase, P. Bryant</creatorcontrib><title>Mandibular muscle troponin of the Florida carpenter ant Camponotus floridanus: extending our insights into invertebrate Ca2+ regulation</title><title>Journal of muscle research and cell motility</title><addtitle>J Muscle Res Cell Motil</addtitle><description>Ants use their mandibles for a variety of functions and behaviors. We investigated mandibular muscle structure and function from major workers of the Florida carpenter ant
Camponotus floridanus
: force-pCa relation and velocity of unloaded shortening of single, permeabilized fibres, primary sequences of troponin subunits (TnC, TnI and TnT) from a mandibular muscle cDNA library, and muscle fibre ultrastructure. From the mechanical measurements, we found Ca
2+
-sensitivity of isometric force was markedly shifted rightward compared with vertebrate striated muscle. From the troponin sequence results, we identified features that could explain the rightward shift of Ca
2+
-activation: the N-helix of TnC is effectively absent and three of the four EF-hands of TnC (sites I, II and III) do not adhere to canonical sequence rules for divalent cation binding; two alternatively spliced isoforms of TnI were identified with the alternatively spliced exon occurring in the region of the IT-arm α-helical coiled-coil, and the N-terminal extension of TnI may be involved in modulation of regulation, as in mammalian cardiac muscle; and TnT has a Glu-rich C-terminus. In addition, a structural homology model was built of
C. floridanus
troponin on the thin filament. From analysis of electron micrographs, we found thick filaments are almost as long as the 6.8 μm sarcomeres, have diameter of ~ 16 nm, and typical center-to-center spacing of ~ 46 nm. These results have implications for the mechanisms by which mandibular muscle fibres perform such a variety of functions, and how the structure of the troponin complex aids in these tasks.</description><subject>Alternative splicing</subject><subject>Animal Anatomy</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>C-Terminus</subject><subject>Calcium-binding protein</subject><subject>Camponotus floridanus</subject><subject>Cardiac muscle</subject><subject>Cell Biology</subject><subject>Filaments</subject><subject>Glycerol</subject><subject>Histology</subject><subject>Homology</subject><subject>Invertebrates</subject><subject>Isoforms</subject><subject>Life Sciences</subject><subject>Mandible</subject><subject>Mechanics</subject><subject>Morphology</subject><subject>Motility</subject><subject>Muscle contraction</subject><subject>Proteomics</subject><subject>Sarcomeres</subject><subject>Skeletal muscle</subject><subject>Structure-function relationships</subject><subject>Troponin</subject><subject>Ultrastructure</subject><subject>Workers (insect caste)</subject><issn>0142-4319</issn><issn>1573-2657</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kcFq3DAQhkVpodukL9CTIJdAcTuSV5KVW1matJCQS3MWWnm8cfBKG0lu0ifIa2dSFwo99CKJ4fv_mdHP2AcBnwSA-VwEWLNuQIoGrAbdPLxiK6FM20itzGu2ArGWzboV9i17V8odACgr5Yo9XfnYj9t58pnv5xIm5DWnQ4pj5Gng9Rb5-ZTy2HsefD5grJi5j5Vv_J6oVOfChwWIcznj-FiRDOOOpznzMZZxd1sLPWqi4yfmitvsK5JefuQZd9S5jikeszeDnwq-_3MfsZvzrz8235rL64vvmy-XTZCdrE2vQfh1H6yVInQi6K3WLYpBUN3KrqPVdauMUIBhCDgEMFSz3Xboje3oP47Y6eJ7yOl-xlLdfiwBp8lHTHNxUikhwQqtCD35B72jnSJN90IZbZTqgCi5UCGnUjIO7pDHvc-_nAD3ko1bsnGUjfudjXsgUbuICsFxh_mv9X9Uz14Jk9o</recordid><startdate>20210601</startdate><enddate>20210601</enddate><creator>Shi, Yun</creator><creator>Bethea, Julia P.</creator><creator>Hetzel-Ebben, Hannah L.</creator><creator>Landim-Vieira, Maicon</creator><creator>Mayper, Ross J.</creator><creator>Williams, Regan L.</creator><creator>Kessler, Lauren E.</creator><creator>Ruiz, Amanda M.</creator><creator>Gargiulo, Kathryn</creator><creator>Rose, Jennifer S. 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Bryant</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-d601a4dc9921c81c6b663e1f160192886066357150ecfcefc0786098bfd798573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alternative splicing</topic><topic>Animal Anatomy</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>C-Terminus</topic><topic>Calcium-binding protein</topic><topic>Camponotus floridanus</topic><topic>Cardiac muscle</topic><topic>Cell Biology</topic><topic>Filaments</topic><topic>Glycerol</topic><topic>Histology</topic><topic>Homology</topic><topic>Invertebrates</topic><topic>Isoforms</topic><topic>Life Sciences</topic><topic>Mandible</topic><topic>Mechanics</topic><topic>Morphology</topic><topic>Motility</topic><topic>Muscle contraction</topic><topic>Proteomics</topic><topic>Sarcomeres</topic><topic>Skeletal muscle</topic><topic>Structure-function relationships</topic><topic>Troponin</topic><topic>Ultrastructure</topic><topic>Workers (insect caste)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shi, Yun</creatorcontrib><creatorcontrib>Bethea, Julia P.</creatorcontrib><creatorcontrib>Hetzel-Ebben, Hannah L.</creatorcontrib><creatorcontrib>Landim-Vieira, Maicon</creatorcontrib><creatorcontrib>Mayper, Ross J.</creatorcontrib><creatorcontrib>Williams, Regan L.</creatorcontrib><creatorcontrib>Kessler, Lauren E.</creatorcontrib><creatorcontrib>Ruiz, Amanda M.</creatorcontrib><creatorcontrib>Gargiulo, Kathryn</creatorcontrib><creatorcontrib>Rose, Jennifer S. 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M.</au><au>Platt, Grayson</au><au>Pinto, Jose R.</au><au>Washburn, Brian K.</au><au>Chase, P. Bryant</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mandibular muscle troponin of the Florida carpenter ant Camponotus floridanus: extending our insights into invertebrate Ca2+ regulation</atitle><jtitle>Journal of muscle research and cell motility</jtitle><stitle>J Muscle Res Cell Motil</stitle><date>2021-06-01</date><risdate>2021</risdate><volume>42</volume><issue>2</issue><spage>399</spage><epage>417</epage><pages>399-417</pages><issn>0142-4319</issn><eissn>1573-2657</eissn><abstract>Ants use their mandibles for a variety of functions and behaviors. We investigated mandibular muscle structure and function from major workers of the Florida carpenter ant
Camponotus floridanus
: force-pCa relation and velocity of unloaded shortening of single, permeabilized fibres, primary sequences of troponin subunits (TnC, TnI and TnT) from a mandibular muscle cDNA library, and muscle fibre ultrastructure. From the mechanical measurements, we found Ca
2+
-sensitivity of isometric force was markedly shifted rightward compared with vertebrate striated muscle. From the troponin sequence results, we identified features that could explain the rightward shift of Ca
2+
-activation: the N-helix of TnC is effectively absent and three of the four EF-hands of TnC (sites I, II and III) do not adhere to canonical sequence rules for divalent cation binding; two alternatively spliced isoforms of TnI were identified with the alternatively spliced exon occurring in the region of the IT-arm α-helical coiled-coil, and the N-terminal extension of TnI may be involved in modulation of regulation, as in mammalian cardiac muscle; and TnT has a Glu-rich C-terminus. In addition, a structural homology model was built of
C. floridanus
troponin on the thin filament. From analysis of electron micrographs, we found thick filaments are almost as long as the 6.8 μm sarcomeres, have diameter of ~ 16 nm, and typical center-to-center spacing of ~ 46 nm. These results have implications for the mechanisms by which mandibular muscle fibres perform such a variety of functions, and how the structure of the troponin complex aids in these tasks.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1007/s10974-021-09606-w</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0003-0405-2062</orcidid><orcidid>https://orcid.org/0000-0002-4279-7770</orcidid><orcidid>https://orcid.org/0000-0002-2970-2458</orcidid><orcidid>https://orcid.org/0000-0002-6696-8888</orcidid><orcidid>https://orcid.org/0000-0003-0738-6658</orcidid><orcidid>https://orcid.org/0000-0002-7725-467X</orcidid><orcidid>https://orcid.org/0000-0003-2460-6691</orcidid><orcidid>https://orcid.org/0000-0001-9701-561X</orcidid><orcidid>https://orcid.org/0000-0002-8662-3983</orcidid><orcidid>https://orcid.org/0000-0001-9092-4976</orcidid><orcidid>https://orcid.org/0000-0002-8844-0099</orcidid></addata></record> |
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subjects | Alternative splicing Animal Anatomy Biomedical and Life Sciences Biomedicine C-Terminus Calcium-binding protein Camponotus floridanus Cardiac muscle Cell Biology Filaments Glycerol Histology Homology Invertebrates Isoforms Life Sciences Mandible Mechanics Morphology Motility Muscle contraction Proteomics Sarcomeres Skeletal muscle Structure-function relationships Troponin Ultrastructure Workers (insect caste) |
title | Mandibular muscle troponin of the Florida carpenter ant Camponotus floridanus: extending our insights into invertebrate Ca2+ regulation |
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