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Ontogeny of myosin isoform expression and prehensile function in the tail of the gray short-tailed opossum ( Monodelphis domestica )
Terrestrial opossums use their semiprehensile tail for grasping nesting materials as opposed to arboreal maneuvering. We relate the development of this adaptive behavior with ontogenetic changes in myosin heavy chain (MHC) isoform expression from 21 days to adulthood. is expected to demonstrate a pr...
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Published in: | Journal of applied physiology (1985) 2017-09, Vol.123 (3), p.513-525 |
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description | Terrestrial opossums use their semiprehensile tail for grasping nesting materials as opposed to arboreal maneuvering. We relate the development of this adaptive behavior with ontogenetic changes in myosin heavy chain (MHC) isoform expression from 21 days to adulthood.
is expected to demonstrate a progressive ability to flex the distal tail up to age 7 mo, when it should exhibit routine nest construction. We hypothesize that juvenile stages (3-7 mo) will be characterized by retention of the neonatal isoform (MHC-Neo), along with predominant expression of fast MHC-2X and -2B, which will transition into greater MHC-1β and -2A isoform content as development progresses. This hypothesis was tested using Q-PCR to quantify and compare gene expression of each isoform with its protein content determined by gel electrophoresis and densitometry. These data were correlated with nesting activity in an age-matched sample of each age group studied. Shifts in regulation of MHC gene transcripts matched well with isoform expression. Notably, mRNA for MHC-Neo and -2B decrease, resulting in little-to-no isoform translation after age 7 mo, whereas mRNA for MHC-1β and -2A increase, and this corresponds with subtle increases in content for these isoforms into late adulthood. Despite the tail remaining intrinsically fast-contracting, a critical growth period for isoform transition is observed between 7 and 13 mo, correlating primarily with use of the tail during nesting activities. Functional transitions in MHC isoforms and fiber type properties may be associated with muscle "tuning" repetitive nest remodeling tasks requiring sustained contractions of the caudal flexors.
Little is understood about skeletal muscle development as it pertains to tail prehensility in mammals. This study uses an integrative approach of relating both MHC gene and protein expression with behavioral and morphometric changes to reveal a predominant fast MHC expression with subtle isoform transitions in caudal muscle across ontogeny. The functional shifts observed are most notably correlated with increased tail grasping for nesting activities. |
doi_str_mv | 10.1152/japplphysiol.00651.2016 |
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is expected to demonstrate a progressive ability to flex the distal tail up to age 7 mo, when it should exhibit routine nest construction. We hypothesize that juvenile stages (3-7 mo) will be characterized by retention of the neonatal isoform (MHC-Neo), along with predominant expression of fast MHC-2X and -2B, which will transition into greater MHC-1β and -2A isoform content as development progresses. This hypothesis was tested using Q-PCR to quantify and compare gene expression of each isoform with its protein content determined by gel electrophoresis and densitometry. These data were correlated with nesting activity in an age-matched sample of each age group studied. Shifts in regulation of MHC gene transcripts matched well with isoform expression. Notably, mRNA for MHC-Neo and -2B decrease, resulting in little-to-no isoform translation after age 7 mo, whereas mRNA for MHC-1β and -2A increase, and this corresponds with subtle increases in content for these isoforms into late adulthood. Despite the tail remaining intrinsically fast-contracting, a critical growth period for isoform transition is observed between 7 and 13 mo, correlating primarily with use of the tail during nesting activities. Functional transitions in MHC isoforms and fiber type properties may be associated with muscle "tuning" repetitive nest remodeling tasks requiring sustained contractions of the caudal flexors.
Little is understood about skeletal muscle development as it pertains to tail prehensility in mammals. This study uses an integrative approach of relating both MHC gene and protein expression with behavioral and morphometric changes to reveal a predominant fast MHC expression with subtle isoform transitions in caudal muscle across ontogeny. The functional shifts observed are most notably correlated with increased tail grasping for nesting activities.</description><identifier>ISSN: 8750-7587</identifier><identifier>EISSN: 1522-1601</identifier><identifier>DOI: 10.1152/japplphysiol.00651.2016</identifier><identifier>PMID: 28522766</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Age ; Animals ; Densitometers ; Densitometry ; Female ; Flexors ; Gel electrophoresis ; Gene Expression ; Grasping ; Hand Strength - physiology ; Isoforms ; Male ; Monodelphis - physiology ; Monodelphis domestica ; Morphogenesis ; Muscular system ; Myosin ; Myosin Heavy Chains - biosynthesis ; Myosin Heavy Chains - genetics ; Myosins - biosynthesis ; Myosins - genetics ; Neonates ; Nesting ; Ontogeny ; Protein Isoforms - biosynthesis ; Protein Isoforms - genetics ; Proteins ; Tail - physiology ; Tails ; Terrestrial environments</subject><ispartof>Journal of applied physiology (1985), 2017-09, Vol.123 (3), p.513-525</ispartof><rights>Copyright © 2017 the American Physiological Society.</rights><rights>Copyright American Physiological Society Sep 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-4eefebedbf99daf6a474dddabba81ff66a4911cd405c3ffe4e3f725f59bf16ed3</citedby><cites>FETCH-LOGICAL-c390t-4eefebedbf99daf6a474dddabba81ff66a4911cd405c3ffe4e3f725f59bf16ed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28522766$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thomas, Dylan R</creatorcontrib><creatorcontrib>Chadwell, Brad A</creatorcontrib><creatorcontrib>Walker, Gary R</creatorcontrib><creatorcontrib>Budde, Julio E</creatorcontrib><creatorcontrib>VandeBerg, John L</creatorcontrib><creatorcontrib>Butcher, Michael T</creatorcontrib><title>Ontogeny of myosin isoform expression and prehensile function in the tail of the gray short-tailed opossum ( Monodelphis domestica )</title><title>Journal of applied physiology (1985)</title><addtitle>J Appl Physiol (1985)</addtitle><description>Terrestrial opossums use their semiprehensile tail for grasping nesting materials as opposed to arboreal maneuvering. We relate the development of this adaptive behavior with ontogenetic changes in myosin heavy chain (MHC) isoform expression from 21 days to adulthood.
is expected to demonstrate a progressive ability to flex the distal tail up to age 7 mo, when it should exhibit routine nest construction. We hypothesize that juvenile stages (3-7 mo) will be characterized by retention of the neonatal isoform (MHC-Neo), along with predominant expression of fast MHC-2X and -2B, which will transition into greater MHC-1β and -2A isoform content as development progresses. This hypothesis was tested using Q-PCR to quantify and compare gene expression of each isoform with its protein content determined by gel electrophoresis and densitometry. These data were correlated with nesting activity in an age-matched sample of each age group studied. Shifts in regulation of MHC gene transcripts matched well with isoform expression. Notably, mRNA for MHC-Neo and -2B decrease, resulting in little-to-no isoform translation after age 7 mo, whereas mRNA for MHC-1β and -2A increase, and this corresponds with subtle increases in content for these isoforms into late adulthood. Despite the tail remaining intrinsically fast-contracting, a critical growth period for isoform transition is observed between 7 and 13 mo, correlating primarily with use of the tail during nesting activities. Functional transitions in MHC isoforms and fiber type properties may be associated with muscle "tuning" repetitive nest remodeling tasks requiring sustained contractions of the caudal flexors.
Little is understood about skeletal muscle development as it pertains to tail prehensility in mammals. This study uses an integrative approach of relating both MHC gene and protein expression with behavioral and morphometric changes to reveal a predominant fast MHC expression with subtle isoform transitions in caudal muscle across ontogeny. The functional shifts observed are most notably correlated with increased tail grasping for nesting activities.</description><subject>Age</subject><subject>Animals</subject><subject>Densitometers</subject><subject>Densitometry</subject><subject>Female</subject><subject>Flexors</subject><subject>Gel electrophoresis</subject><subject>Gene Expression</subject><subject>Grasping</subject><subject>Hand Strength - physiology</subject><subject>Isoforms</subject><subject>Male</subject><subject>Monodelphis - physiology</subject><subject>Monodelphis domestica</subject><subject>Morphogenesis</subject><subject>Muscular system</subject><subject>Myosin</subject><subject>Myosin Heavy Chains - biosynthesis</subject><subject>Myosin Heavy Chains - genetics</subject><subject>Myosins - biosynthesis</subject><subject>Myosins - genetics</subject><subject>Neonates</subject><subject>Nesting</subject><subject>Ontogeny</subject><subject>Protein Isoforms - biosynthesis</subject><subject>Protein Isoforms - genetics</subject><subject>Proteins</subject><subject>Tail - physiology</subject><subject>Tails</subject><subject>Terrestrial environments</subject><issn>8750-7587</issn><issn>1522-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpdkUtPxCAUhYnR6Pj4C0riRhcdoaW0LM3EV6Jxo-uGlovDpIUKbWL3_nCprxhXwOG75144CJ1QsqQ0Ty82su_bfj0F49olITyny5RQvoUW8TZNKCd0Gy3KIidJkZfFHtoPYUMIZSynu2gvLSNVcL5A7492cC9gJ-w07iYXjMUmOO18h-Gt9xBiC4ulVTge1mCDaQHr0TbDrEd6WAMepGlng3n_4uWEw9r5IZllUNj1LoSxw2f4wVmnIA5uAlaugzCYRuLzQ7SjZRvg6Hs9QM_XV0-r2-T-8eZudXmfNJkgQ8IANNSgai2EkppLVjCllKxrWVKteRQEpY1iJG8yrYFBpos017moNeWgsgN09uXbe_c6xu5VZ0IDbSstuDFUVBBSZoKVaURP_6EbN3obp4tU_G4mBCeRKr6oxscnetBV700n_VRRUs1BVX-Dqj6DquagYuXxt_9Yd6B-636SyT4A5GaW5g</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Thomas, Dylan R</creator><creator>Chadwell, Brad A</creator><creator>Walker, Gary R</creator><creator>Budde, Julio E</creator><creator>VandeBerg, John L</creator><creator>Butcher, Michael T</creator><general>American Physiological 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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20170901</creationdate><title>Ontogeny of myosin isoform expression and prehensile function in the tail of the gray short-tailed opossum ( Monodelphis domestica )</title><author>Thomas, Dylan R ; Chadwell, Brad A ; Walker, Gary R ; Budde, Julio E ; VandeBerg, John L ; Butcher, Michael T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-4eefebedbf99daf6a474dddabba81ff66a4911cd405c3ffe4e3f725f59bf16ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Age</topic><topic>Animals</topic><topic>Densitometers</topic><topic>Densitometry</topic><topic>Female</topic><topic>Flexors</topic><topic>Gel electrophoresis</topic><topic>Gene Expression</topic><topic>Grasping</topic><topic>Hand Strength - physiology</topic><topic>Isoforms</topic><topic>Male</topic><topic>Monodelphis - physiology</topic><topic>Monodelphis domestica</topic><topic>Morphogenesis</topic><topic>Muscular system</topic><topic>Myosin</topic><topic>Myosin Heavy Chains - biosynthesis</topic><topic>Myosin Heavy Chains - genetics</topic><topic>Myosins - biosynthesis</topic><topic>Myosins - genetics</topic><topic>Neonates</topic><topic>Nesting</topic><topic>Ontogeny</topic><topic>Protein Isoforms - biosynthesis</topic><topic>Protein Isoforms - genetics</topic><topic>Proteins</topic><topic>Tail - physiology</topic><topic>Tails</topic><topic>Terrestrial environments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thomas, Dylan R</creatorcontrib><creatorcontrib>Chadwell, Brad A</creatorcontrib><creatorcontrib>Walker, Gary R</creatorcontrib><creatorcontrib>Budde, Julio E</creatorcontrib><creatorcontrib>VandeBerg, John L</creatorcontrib><creatorcontrib>Butcher, Michael T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of applied physiology (1985)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thomas, Dylan R</au><au>Chadwell, Brad A</au><au>Walker, Gary R</au><au>Budde, Julio E</au><au>VandeBerg, John L</au><au>Butcher, Michael T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ontogeny of myosin isoform expression and prehensile function in the tail of the gray short-tailed opossum ( Monodelphis domestica )</atitle><jtitle>Journal of applied physiology (1985)</jtitle><addtitle>J Appl Physiol (1985)</addtitle><date>2017-09-01</date><risdate>2017</risdate><volume>123</volume><issue>3</issue><spage>513</spage><epage>525</epage><pages>513-525</pages><issn>8750-7587</issn><eissn>1522-1601</eissn><abstract>Terrestrial opossums use their semiprehensile tail for grasping nesting materials as opposed to arboreal maneuvering. We relate the development of this adaptive behavior with ontogenetic changes in myosin heavy chain (MHC) isoform expression from 21 days to adulthood.
is expected to demonstrate a progressive ability to flex the distal tail up to age 7 mo, when it should exhibit routine nest construction. We hypothesize that juvenile stages (3-7 mo) will be characterized by retention of the neonatal isoform (MHC-Neo), along with predominant expression of fast MHC-2X and -2B, which will transition into greater MHC-1β and -2A isoform content as development progresses. This hypothesis was tested using Q-PCR to quantify and compare gene expression of each isoform with its protein content determined by gel electrophoresis and densitometry. These data were correlated with nesting activity in an age-matched sample of each age group studied. Shifts in regulation of MHC gene transcripts matched well with isoform expression. Notably, mRNA for MHC-Neo and -2B decrease, resulting in little-to-no isoform translation after age 7 mo, whereas mRNA for MHC-1β and -2A increase, and this corresponds with subtle increases in content for these isoforms into late adulthood. Despite the tail remaining intrinsically fast-contracting, a critical growth period for isoform transition is observed between 7 and 13 mo, correlating primarily with use of the tail during nesting activities. Functional transitions in MHC isoforms and fiber type properties may be associated with muscle "tuning" repetitive nest remodeling tasks requiring sustained contractions of the caudal flexors.
Little is understood about skeletal muscle development as it pertains to tail prehensility in mammals. This study uses an integrative approach of relating both MHC gene and protein expression with behavioral and morphometric changes to reveal a predominant fast MHC expression with subtle isoform transitions in caudal muscle across ontogeny. The functional shifts observed are most notably correlated with increased tail grasping for nesting activities.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>28522766</pmid><doi>10.1152/japplphysiol.00651.2016</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Age Animals Densitometers Densitometry Female Flexors Gel electrophoresis Gene Expression Grasping Hand Strength - physiology Isoforms Male Monodelphis - physiology Monodelphis domestica Morphogenesis Muscular system Myosin Myosin Heavy Chains - biosynthesis Myosin Heavy Chains - genetics Myosins - biosynthesis Myosins - genetics Neonates Nesting Ontogeny Protein Isoforms - biosynthesis Protein Isoforms - genetics Proteins Tail - physiology Tails Terrestrial environments |
title | Ontogeny of myosin isoform expression and prehensile function in the tail of the gray short-tailed opossum ( Monodelphis domestica ) |
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