Loading…

Genome duplication events have led to a diversification in the CPT I gene family in fish

The enzyme carnitine palmitoyltransferase (CPT) I is a major regulator of mitochondrial fatty acid oxidation in vertebrates. Numerous genome duplication events throughout evolution have given rise to three (in mammals) or multiple (in fish) genetically and functionally different isoforms of this enz...

Full description

Saved in:
Bibliographic Details
Published in:American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2010-08, Vol.299 (2), p.R579-R589
Main Authors: Morash, Andrea J, Le Moine, Christophe M R, McClelland, Grant B
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c329t-92bba386a109a69749588c645985357fd669dbb49a04987fd45a82c0ec1f8ea93
cites cdi_FETCH-LOGICAL-c329t-92bba386a109a69749588c645985357fd669dbb49a04987fd45a82c0ec1f8ea93
container_end_page R589
container_issue 2
container_start_page R579
container_title American journal of physiology. Regulatory, integrative and comparative physiology
container_volume 299
creator Morash, Andrea J
Le Moine, Christophe M R
McClelland, Grant B
description The enzyme carnitine palmitoyltransferase (CPT) I is a major regulator of mitochondrial fatty acid oxidation in vertebrates. Numerous genome duplication events throughout evolution have given rise to three (in mammals) or multiple (in fish) genetically and functionally different isoforms of this enzyme. In particular, these isoforms represent a diversification of kinetic and regulatory properties stemming from mutations at the genomic and proteomic levels. Phylogenetic reconstructions reveal a comprehensive view of the CPT I family in vertebrates and genomic modifications leading to structural changes in proteins and functional differences between tissues and taxa. In a model fish species (rainbow trout), the presence of five CPT I isoforms suggests repeated duplication events in bony fishes and salmonids. Subsequently, an array of nucleotide and amino acid substitutions in the isoforms may contribute to a tissue-specific and a previously observed species-specific difference in the IC(50) for malonyl-CoA. Moreover, all five isoforms are expressed in trout at the mRNA level in skeletal muscle, heart, liver, kidney, and intestine. In general, transcript levels of the beta-isoforms were higher in muscle tissues, while levels of the alpha-isoforms were higher in other tissues. Rainbow trout also exhibit developmental plasticity in relative mRNA expression of CPT I isoforms from fry to juvenile to adult stage. Thus the evolution of CPT I has resulted in a very diverse family of isoforms. These differences represent a degree of specificity in the ability of species to regulate function at the protein and tissue levels, which, in turn, may allow for precise control of lipid oxidation in individual tissues during physiological perturbations.
doi_str_mv 10.1152/ajpregu.00088.2010
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_748933619</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>748933619</sourcerecordid><originalsourceid>FETCH-LOGICAL-c329t-92bba386a109a69749588c645985357fd669dbb49a04987fd45a82c0ec1f8ea93</originalsourceid><addsrcrecordid>eNpdkE1Lw0AQhhdRbK3-AQ-yePGUul_Z7B6laC0U9FDB27JJJu2WfNTdpNB_b2KrB0_DMM_7MjwI3VIypTRmj3a787DupoQQpaaMUHKGxv2BRVRoco7GhEseSUr1CF2FsO05wQW_RCNGYqq5FGP0OYe6qQDn3a50mW1dU2PYQ90GvLF7wCXkuG2wxbnbgw-u-IVcjdsN4Nn7Ci_wGmrAha1ceRgOhQuba3RR2DLAzWlO0MfL82r2Gi3f5ovZ0zLKONNtpFmaWq6kpURbqROhY6UyKWKtYh4nRS6lztNUaEuEVv0uYqtYRiCjhQKr-QQ9HHt3vvnqILSmciGDsrQ1NF0wiVCac0kH8v4fuW06X_fPmYQLlXAmkh5iRyjzTQgeCrPzrrL-YCgxg3Vzsm5-rJvBeh-6OzV3aQX5X-RXM_8Gmbd9mA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>734873247</pqid></control><display><type>article</type><title>Genome duplication events have led to a diversification in the CPT I gene family in fish</title><source>American Physiological Society Free</source><creator>Morash, Andrea J ; Le Moine, Christophe M R ; McClelland, Grant B</creator><creatorcontrib>Morash, Andrea J ; Le Moine, Christophe M R ; McClelland, Grant B</creatorcontrib><description>The enzyme carnitine palmitoyltransferase (CPT) I is a major regulator of mitochondrial fatty acid oxidation in vertebrates. Numerous genome duplication events throughout evolution have given rise to three (in mammals) or multiple (in fish) genetically and functionally different isoforms of this enzyme. In particular, these isoforms represent a diversification of kinetic and regulatory properties stemming from mutations at the genomic and proteomic levels. Phylogenetic reconstructions reveal a comprehensive view of the CPT I family in vertebrates and genomic modifications leading to structural changes in proteins and functional differences between tissues and taxa. In a model fish species (rainbow trout), the presence of five CPT I isoforms suggests repeated duplication events in bony fishes and salmonids. Subsequently, an array of nucleotide and amino acid substitutions in the isoforms may contribute to a tissue-specific and a previously observed species-specific difference in the IC(50) for malonyl-CoA. Moreover, all five isoforms are expressed in trout at the mRNA level in skeletal muscle, heart, liver, kidney, and intestine. In general, transcript levels of the beta-isoforms were higher in muscle tissues, while levels of the alpha-isoforms were higher in other tissues. Rainbow trout also exhibit developmental plasticity in relative mRNA expression of CPT I isoforms from fry to juvenile to adult stage. Thus the evolution of CPT I has resulted in a very diverse family of isoforms. These differences represent a degree of specificity in the ability of species to regulate function at the protein and tissue levels, which, in turn, may allow for precise control of lipid oxidation in individual tissues during physiological perturbations.</description><identifier>ISSN: 0363-6119</identifier><identifier>EISSN: 1522-1490</identifier><identifier>DOI: 10.1152/ajpregu.00088.2010</identifier><identifier>PMID: 20519364</identifier><identifier>CODEN: AJPRDO</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Age Factors ; Amino Acid Sequence ; Animals ; Carnitine O-Palmitoyltransferase - chemistry ; Carnitine O-Palmitoyltransferase - genetics ; Carnitine O-Palmitoyltransferase - metabolism ; Enzymes ; Evolution, Molecular ; Fatty acids ; Fish Proteins - chemistry ; Fish Proteins - genetics ; Fish Proteins - metabolism ; Gene Duplication ; Gene Expression Regulation, Developmental ; Gene Expression Regulation, Enzymologic ; Genomics ; Genotype ; Isoenzymes ; Kinetics ; Malonyl Coenzyme A - metabolism ; Molecular Sequence Data ; Oncorhynchus mykiss - genetics ; Oncorhynchus mykiss - growth &amp; development ; Oncorhynchus mykiss - metabolism ; Oxidation ; Phenotype ; Phylogeny ; Protein Conformation ; RNA, Messenger - metabolism ; Species Specificity ; Structure-Activity Relationship ; Tissues ; Trout</subject><ispartof>American journal of physiology. Regulatory, integrative and comparative physiology, 2010-08, Vol.299 (2), p.R579-R589</ispartof><rights>Copyright American Physiological Society Aug 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c329t-92bba386a109a69749588c645985357fd669dbb49a04987fd45a82c0ec1f8ea93</citedby><cites>FETCH-LOGICAL-c329t-92bba386a109a69749588c645985357fd669dbb49a04987fd45a82c0ec1f8ea93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20519364$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morash, Andrea J</creatorcontrib><creatorcontrib>Le Moine, Christophe M R</creatorcontrib><creatorcontrib>McClelland, Grant B</creatorcontrib><title>Genome duplication events have led to a diversification in the CPT I gene family in fish</title><title>American journal of physiology. Regulatory, integrative and comparative physiology</title><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><description>The enzyme carnitine palmitoyltransferase (CPT) I is a major regulator of mitochondrial fatty acid oxidation in vertebrates. Numerous genome duplication events throughout evolution have given rise to three (in mammals) or multiple (in fish) genetically and functionally different isoforms of this enzyme. In particular, these isoforms represent a diversification of kinetic and regulatory properties stemming from mutations at the genomic and proteomic levels. Phylogenetic reconstructions reveal a comprehensive view of the CPT I family in vertebrates and genomic modifications leading to structural changes in proteins and functional differences between tissues and taxa. In a model fish species (rainbow trout), the presence of five CPT I isoforms suggests repeated duplication events in bony fishes and salmonids. Subsequently, an array of nucleotide and amino acid substitutions in the isoforms may contribute to a tissue-specific and a previously observed species-specific difference in the IC(50) for malonyl-CoA. Moreover, all five isoforms are expressed in trout at the mRNA level in skeletal muscle, heart, liver, kidney, and intestine. In general, transcript levels of the beta-isoforms were higher in muscle tissues, while levels of the alpha-isoforms were higher in other tissues. Rainbow trout also exhibit developmental plasticity in relative mRNA expression of CPT I isoforms from fry to juvenile to adult stage. Thus the evolution of CPT I has resulted in a very diverse family of isoforms. These differences represent a degree of specificity in the ability of species to regulate function at the protein and tissue levels, which, in turn, may allow for precise control of lipid oxidation in individual tissues during physiological perturbations.</description><subject>Age Factors</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Carnitine O-Palmitoyltransferase - chemistry</subject><subject>Carnitine O-Palmitoyltransferase - genetics</subject><subject>Carnitine O-Palmitoyltransferase - metabolism</subject><subject>Enzymes</subject><subject>Evolution, Molecular</subject><subject>Fatty acids</subject><subject>Fish Proteins - chemistry</subject><subject>Fish Proteins - genetics</subject><subject>Fish Proteins - metabolism</subject><subject>Gene Duplication</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Gene Expression Regulation, Enzymologic</subject><subject>Genomics</subject><subject>Genotype</subject><subject>Isoenzymes</subject><subject>Kinetics</subject><subject>Malonyl Coenzyme A - metabolism</subject><subject>Molecular Sequence Data</subject><subject>Oncorhynchus mykiss - genetics</subject><subject>Oncorhynchus mykiss - growth &amp; development</subject><subject>Oncorhynchus mykiss - metabolism</subject><subject>Oxidation</subject><subject>Phenotype</subject><subject>Phylogeny</subject><subject>Protein Conformation</subject><subject>RNA, Messenger - metabolism</subject><subject>Species Specificity</subject><subject>Structure-Activity Relationship</subject><subject>Tissues</subject><subject>Trout</subject><issn>0363-6119</issn><issn>1522-1490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNpdkE1Lw0AQhhdRbK3-AQ-yePGUul_Z7B6laC0U9FDB27JJJu2WfNTdpNB_b2KrB0_DMM_7MjwI3VIypTRmj3a787DupoQQpaaMUHKGxv2BRVRoco7GhEseSUr1CF2FsO05wQW_RCNGYqq5FGP0OYe6qQDn3a50mW1dU2PYQ90GvLF7wCXkuG2wxbnbgw-u-IVcjdsN4Nn7Ci_wGmrAha1ceRgOhQuba3RR2DLAzWlO0MfL82r2Gi3f5ovZ0zLKONNtpFmaWq6kpURbqROhY6UyKWKtYh4nRS6lztNUaEuEVv0uYqtYRiCjhQKr-QQ9HHt3vvnqILSmciGDsrQ1NF0wiVCac0kH8v4fuW06X_fPmYQLlXAmkh5iRyjzTQgeCrPzrrL-YCgxg3Vzsm5-rJvBeh-6OzV3aQX5X-RXM_8Gmbd9mA</recordid><startdate>201008</startdate><enddate>201008</enddate><creator>Morash, Andrea J</creator><creator>Le Moine, Christophe M R</creator><creator>McClelland, Grant B</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>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201008</creationdate><title>Genome duplication events have led to a diversification in the CPT I gene family in fish</title><author>Morash, Andrea J ; Le Moine, Christophe M R ; McClelland, Grant B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c329t-92bba386a109a69749588c645985357fd669dbb49a04987fd45a82c0ec1f8ea93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Age Factors</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Carnitine O-Palmitoyltransferase - chemistry</topic><topic>Carnitine O-Palmitoyltransferase - genetics</topic><topic>Carnitine O-Palmitoyltransferase - metabolism</topic><topic>Enzymes</topic><topic>Evolution, Molecular</topic><topic>Fatty acids</topic><topic>Fish Proteins - chemistry</topic><topic>Fish Proteins - genetics</topic><topic>Fish Proteins - metabolism</topic><topic>Gene Duplication</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Gene Expression Regulation, Enzymologic</topic><topic>Genomics</topic><topic>Genotype</topic><topic>Isoenzymes</topic><topic>Kinetics</topic><topic>Malonyl Coenzyme A - metabolism</topic><topic>Molecular Sequence Data</topic><topic>Oncorhynchus mykiss - genetics</topic><topic>Oncorhynchus mykiss - growth &amp; development</topic><topic>Oncorhynchus mykiss - metabolism</topic><topic>Oxidation</topic><topic>Phenotype</topic><topic>Phylogeny</topic><topic>Protein Conformation</topic><topic>RNA, Messenger - metabolism</topic><topic>Species Specificity</topic><topic>Structure-Activity Relationship</topic><topic>Tissues</topic><topic>Trout</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morash, Andrea J</creatorcontrib><creatorcontrib>Le Moine, Christophe M R</creatorcontrib><creatorcontrib>McClelland, Grant B</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 &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception 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>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morash, Andrea J</au><au>Le Moine, Christophe M R</au><au>McClelland, Grant B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome duplication events have led to a diversification in the CPT I gene family in fish</atitle><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><date>2010-08</date><risdate>2010</risdate><volume>299</volume><issue>2</issue><spage>R579</spage><epage>R589</epage><pages>R579-R589</pages><issn>0363-6119</issn><eissn>1522-1490</eissn><coden>AJPRDO</coden><abstract>The enzyme carnitine palmitoyltransferase (CPT) I is a major regulator of mitochondrial fatty acid oxidation in vertebrates. Numerous genome duplication events throughout evolution have given rise to three (in mammals) or multiple (in fish) genetically and functionally different isoforms of this enzyme. In particular, these isoforms represent a diversification of kinetic and regulatory properties stemming from mutations at the genomic and proteomic levels. Phylogenetic reconstructions reveal a comprehensive view of the CPT I family in vertebrates and genomic modifications leading to structural changes in proteins and functional differences between tissues and taxa. In a model fish species (rainbow trout), the presence of five CPT I isoforms suggests repeated duplication events in bony fishes and salmonids. Subsequently, an array of nucleotide and amino acid substitutions in the isoforms may contribute to a tissue-specific and a previously observed species-specific difference in the IC(50) for malonyl-CoA. Moreover, all five isoforms are expressed in trout at the mRNA level in skeletal muscle, heart, liver, kidney, and intestine. In general, transcript levels of the beta-isoforms were higher in muscle tissues, while levels of the alpha-isoforms were higher in other tissues. Rainbow trout also exhibit developmental plasticity in relative mRNA expression of CPT I isoforms from fry to juvenile to adult stage. Thus the evolution of CPT I has resulted in a very diverse family of isoforms. These differences represent a degree of specificity in the ability of species to regulate function at the protein and tissue levels, which, in turn, may allow for precise control of lipid oxidation in individual tissues during physiological perturbations.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>20519364</pmid><doi>10.1152/ajpregu.00088.2010</doi></addata></record>
fulltext fulltext
identifier ISSN: 0363-6119
ispartof American journal of physiology. Regulatory, integrative and comparative physiology, 2010-08, Vol.299 (2), p.R579-R589
issn 0363-6119
1522-1490
language eng
recordid cdi_proquest_miscellaneous_748933619
source American Physiological Society Free
subjects Age Factors
Amino Acid Sequence
Animals
Carnitine O-Palmitoyltransferase - chemistry
Carnitine O-Palmitoyltransferase - genetics
Carnitine O-Palmitoyltransferase - metabolism
Enzymes
Evolution, Molecular
Fatty acids
Fish Proteins - chemistry
Fish Proteins - genetics
Fish Proteins - metabolism
Gene Duplication
Gene Expression Regulation, Developmental
Gene Expression Regulation, Enzymologic
Genomics
Genotype
Isoenzymes
Kinetics
Malonyl Coenzyme A - metabolism
Molecular Sequence Data
Oncorhynchus mykiss - genetics
Oncorhynchus mykiss - growth & development
Oncorhynchus mykiss - metabolism
Oxidation
Phenotype
Phylogeny
Protein Conformation
RNA, Messenger - metabolism
Species Specificity
Structure-Activity Relationship
Tissues
Trout
title Genome duplication events have led to a diversification in the CPT I gene family in fish
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T23%3A02%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genome%20duplication%20events%20have%20led%20to%20a%20diversification%20in%20the%20CPT%20I%20gene%20family%20in%20fish&rft.jtitle=American%20journal%20of%20physiology.%20Regulatory,%20integrative%20and%20comparative%20physiology&rft.au=Morash,%20Andrea%20J&rft.date=2010-08&rft.volume=299&rft.issue=2&rft.spage=R579&rft.epage=R589&rft.pages=R579-R589&rft.issn=0363-6119&rft.eissn=1522-1490&rft.coden=AJPRDO&rft_id=info:doi/10.1152/ajpregu.00088.2010&rft_dat=%3Cproquest_cross%3E748933619%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c329t-92bba386a109a69749588c645985357fd669dbb49a04987fd45a82c0ec1f8ea93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=734873247&rft_id=info:pmid/20519364&rfr_iscdi=true