Evolution of the arginine kinase gene family
Arginine kinase (AK), catalyzing the reversible transfer of phosphate from MgATP to arginine yielding phosphoarginine and MgADP, is widely distributed throughout the invertebrates and is also present in certain protozoa. Typically, these proteins are found as monomers targeted to the cytoplasm, but...
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Veröffentlicht in: | Comparative biochemistry and physiology. Part D, Genomics & proteomics Genomics & proteomics, 2006-06, Vol.1 (2), p.209-218 |
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creator | Uda, Kouji Fujimoto, Naka Akiyama, Youhei Mizuta, Kanae Tanaka, Kumiko Ellington, W. Ross Suzuki, Tomohiko |
description | Arginine kinase (AK), catalyzing the reversible transfer of phosphate from MgATP to arginine yielding phosphoarginine and MgADP, is widely distributed throughout the invertebrates and is also present in certain protozoa. Typically, these proteins are found as monomers targeted to the cytoplasm, but true dimeric and contiguous dimeric AKs as well as mitochondrial AK activities have been observed. In the present study, we have obtained the sequences of the genes for AKs from two distantly related molluscs—the cephalopod
Nautilus pompilius and the bivalve
Crassostrea gigas. These new data were combined with available gene structure data (exon/intron organization) extracted from EST and genome sequencing project databases. These data, comprised of 23 sequences and gene structures from Protozoa, Cnidaria, Platyhelminthes, Mollusca, Arthropoda and Nematoda, provide great insight into the evolution and divergence of the AK family. Sequence and phylogenetic analyses clearly show that the AKs are homologous having arisen from some common ancestor. However, AK gene organization is highly divergent and variable. Molluscan AK genes typically have a highly conserved six-exon/five-intron organization, a structure that is very similar to that of the platyhelminth
Schistosoma mansoni Arthropod and nematode AK genes have fewer introns, while the cnidarian and protozoan genes each display unique exon/intron organization when compared to the other AK genes. The non-conservative nature of the AK genes is in sharp contrast to the relatively high degree of conservation of intron positions seen in a homologous enzyme creatine kinase (CK). The present results also show that gene duplication and subsequent fusion events forming unusual two-domain AKs occurred independently at least four times as these contiguous dimers are present in Protozoa, Cnidaria, Platyhelminthes and Mollusca. Detailed analyses of the amino acid sequences indicate that two AKs (one each from
Drosophila and
Caenorhabditis) have what appear to be N-terminal mitochondrial targeting sequences, providing the first evidence for true mitochondrial AK genes. The AK gene family is ancient and the lineage has undergone considerable divergence as well as multiple duplication and fusion events. |
doi_str_mv | 10.1016/j.cbd.2005.10.007 |
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Nautilus pompilius and the bivalve
Crassostrea gigas. These new data were combined with available gene structure data (exon/intron organization) extracted from EST and genome sequencing project databases. These data, comprised of 23 sequences and gene structures from Protozoa, Cnidaria, Platyhelminthes, Mollusca, Arthropoda and Nematoda, provide great insight into the evolution and divergence of the AK family. Sequence and phylogenetic analyses clearly show that the AKs are homologous having arisen from some common ancestor. However, AK gene organization is highly divergent and variable. Molluscan AK genes typically have a highly conserved six-exon/five-intron organization, a structure that is very similar to that of the platyhelminth
Schistosoma mansoni Arthropod and nematode AK genes have fewer introns, while the cnidarian and protozoan genes each display unique exon/intron organization when compared to the other AK genes. The non-conservative nature of the AK genes is in sharp contrast to the relatively high degree of conservation of intron positions seen in a homologous enzyme creatine kinase (CK). The present results also show that gene duplication and subsequent fusion events forming unusual two-domain AKs occurred independently at least four times as these contiguous dimers are present in Protozoa, Cnidaria, Platyhelminthes and Mollusca. Detailed analyses of the amino acid sequences indicate that two AKs (one each from
Drosophila and
Caenorhabditis) have what appear to be N-terminal mitochondrial targeting sequences, providing the first evidence for true mitochondrial AK genes. The AK gene family is ancient and the lineage has undergone considerable divergence as well as multiple duplication and fusion events.</description><identifier>ISSN: 1744-117X</identifier><identifier>EISSN: 1878-0407</identifier><identifier>DOI: 10.1016/j.cbd.2005.10.007</identifier><identifier>PMID: 20483252</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Arginine kinase ; Creatine kinase ; Exon/intron organization ; Gene ; Phosphagen kinase</subject><ispartof>Comparative biochemistry and physiology. Part D, Genomics & proteomics, 2006-06, Vol.1 (2), p.209-218</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-f37125f4617b2b71878beba2e18f0a36e3271968c2a690b4c21e0a666fc8e2b93</citedby><cites>FETCH-LOGICAL-c418t-f37125f4617b2b71878beba2e18f0a36e3271968c2a690b4c21e0a666fc8e2b93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1744117X05000250$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20483252$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uda, Kouji</creatorcontrib><creatorcontrib>Fujimoto, Naka</creatorcontrib><creatorcontrib>Akiyama, Youhei</creatorcontrib><creatorcontrib>Mizuta, Kanae</creatorcontrib><creatorcontrib>Tanaka, Kumiko</creatorcontrib><creatorcontrib>Ellington, W. Ross</creatorcontrib><creatorcontrib>Suzuki, Tomohiko</creatorcontrib><title>Evolution of the arginine kinase gene family</title><title>Comparative biochemistry and physiology. Part D, Genomics & proteomics</title><addtitle>Comp Biochem Physiol Part D Genomics Proteomics</addtitle><description>Arginine kinase (AK), catalyzing the reversible transfer of phosphate from MgATP to arginine yielding phosphoarginine and MgADP, is widely distributed throughout the invertebrates and is also present in certain protozoa. Typically, these proteins are found as monomers targeted to the cytoplasm, but true dimeric and contiguous dimeric AKs as well as mitochondrial AK activities have been observed. In the present study, we have obtained the sequences of the genes for AKs from two distantly related molluscs—the cephalopod
Nautilus pompilius and the bivalve
Crassostrea gigas. These new data were combined with available gene structure data (exon/intron organization) extracted from EST and genome sequencing project databases. These data, comprised of 23 sequences and gene structures from Protozoa, Cnidaria, Platyhelminthes, Mollusca, Arthropoda and Nematoda, provide great insight into the evolution and divergence of the AK family. Sequence and phylogenetic analyses clearly show that the AKs are homologous having arisen from some common ancestor. However, AK gene organization is highly divergent and variable. Molluscan AK genes typically have a highly conserved six-exon/five-intron organization, a structure that is very similar to that of the platyhelminth
Schistosoma mansoni Arthropod and nematode AK genes have fewer introns, while the cnidarian and protozoan genes each display unique exon/intron organization when compared to the other AK genes. The non-conservative nature of the AK genes is in sharp contrast to the relatively high degree of conservation of intron positions seen in a homologous enzyme creatine kinase (CK). The present results also show that gene duplication and subsequent fusion events forming unusual two-domain AKs occurred independently at least four times as these contiguous dimers are present in Protozoa, Cnidaria, Platyhelminthes and Mollusca. Detailed analyses of the amino acid sequences indicate that two AKs (one each from
Drosophila and
Caenorhabditis) have what appear to be N-terminal mitochondrial targeting sequences, providing the first evidence for true mitochondrial AK genes. The AK gene family is ancient and the lineage has undergone considerable divergence as well as multiple duplication and fusion events.</description><subject>Arginine kinase</subject><subject>Creatine kinase</subject><subject>Exon/intron organization</subject><subject>Gene</subject><subject>Phosphagen kinase</subject><issn>1744-117X</issn><issn>1878-0407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EolD4ADYoOzak2I5jO2KFqvKQKrEBiZ1lO5Pikkexk0r9exy1sGQ1d0Z3rmYOQlcEzwgm_G49s6acUYzz2M8wFkfojEghU8ywOI5aMJYSIj4m6DyENcaMFyw_RROKmcxoTs_Q7WLb1UPvujbpqqT_hET7lWtdC8mXa3WAZAVRV7px9e4CnVS6DnB5qFP0_rh4mz-ny9enl_nDMrWMyD6tMkFoXjFOhKFGjBcZMJoCkRXWGYeMClJwaanmBTbMUgJYc84rK4GaIpuim33uxnffA4ReNS5YqGvdQjcEJbIsZ5JLEp1k77S-C8FDpTbeNdrvFMFqZKTWKjJSI6NxFBnFnetD-mAaKP82fqFEw_3eAPHHrQOvgnXQWiidB9ursnP_xP8AAUh1EA</recordid><startdate>20060601</startdate><enddate>20060601</enddate><creator>Uda, Kouji</creator><creator>Fujimoto, Naka</creator><creator>Akiyama, Youhei</creator><creator>Mizuta, Kanae</creator><creator>Tanaka, Kumiko</creator><creator>Ellington, W. Ross</creator><creator>Suzuki, Tomohiko</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20060601</creationdate><title>Evolution of the arginine kinase gene family</title><author>Uda, Kouji ; Fujimoto, Naka ; Akiyama, Youhei ; Mizuta, Kanae ; Tanaka, Kumiko ; Ellington, W. Ross ; Suzuki, Tomohiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-f37125f4617b2b71878beba2e18f0a36e3271968c2a690b4c21e0a666fc8e2b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Arginine kinase</topic><topic>Creatine kinase</topic><topic>Exon/intron organization</topic><topic>Gene</topic><topic>Phosphagen kinase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uda, Kouji</creatorcontrib><creatorcontrib>Fujimoto, Naka</creatorcontrib><creatorcontrib>Akiyama, Youhei</creatorcontrib><creatorcontrib>Mizuta, Kanae</creatorcontrib><creatorcontrib>Tanaka, Kumiko</creatorcontrib><creatorcontrib>Ellington, W. Ross</creatorcontrib><creatorcontrib>Suzuki, Tomohiko</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Comparative biochemistry and physiology. Part D, Genomics & proteomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uda, Kouji</au><au>Fujimoto, Naka</au><au>Akiyama, Youhei</au><au>Mizuta, Kanae</au><au>Tanaka, Kumiko</au><au>Ellington, W. Ross</au><au>Suzuki, Tomohiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evolution of the arginine kinase gene family</atitle><jtitle>Comparative biochemistry and physiology. Part D, Genomics & proteomics</jtitle><addtitle>Comp Biochem Physiol Part D Genomics Proteomics</addtitle><date>2006-06-01</date><risdate>2006</risdate><volume>1</volume><issue>2</issue><spage>209</spage><epage>218</epage><pages>209-218</pages><issn>1744-117X</issn><eissn>1878-0407</eissn><abstract>Arginine kinase (AK), catalyzing the reversible transfer of phosphate from MgATP to arginine yielding phosphoarginine and MgADP, is widely distributed throughout the invertebrates and is also present in certain protozoa. Typically, these proteins are found as monomers targeted to the cytoplasm, but true dimeric and contiguous dimeric AKs as well as mitochondrial AK activities have been observed. In the present study, we have obtained the sequences of the genes for AKs from two distantly related molluscs—the cephalopod
Nautilus pompilius and the bivalve
Crassostrea gigas. These new data were combined with available gene structure data (exon/intron organization) extracted from EST and genome sequencing project databases. These data, comprised of 23 sequences and gene structures from Protozoa, Cnidaria, Platyhelminthes, Mollusca, Arthropoda and Nematoda, provide great insight into the evolution and divergence of the AK family. Sequence and phylogenetic analyses clearly show that the AKs are homologous having arisen from some common ancestor. However, AK gene organization is highly divergent and variable. Molluscan AK genes typically have a highly conserved six-exon/five-intron organization, a structure that is very similar to that of the platyhelminth
Schistosoma mansoni Arthropod and nematode AK genes have fewer introns, while the cnidarian and protozoan genes each display unique exon/intron organization when compared to the other AK genes. The non-conservative nature of the AK genes is in sharp contrast to the relatively high degree of conservation of intron positions seen in a homologous enzyme creatine kinase (CK). The present results also show that gene duplication and subsequent fusion events forming unusual two-domain AKs occurred independently at least four times as these contiguous dimers are present in Protozoa, Cnidaria, Platyhelminthes and Mollusca. Detailed analyses of the amino acid sequences indicate that two AKs (one each from
Drosophila and
Caenorhabditis) have what appear to be N-terminal mitochondrial targeting sequences, providing the first evidence for true mitochondrial AK genes. The AK gene family is ancient and the lineage has undergone considerable divergence as well as multiple duplication and fusion events.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>20483252</pmid><doi>10.1016/j.cbd.2005.10.007</doi><tpages>10</tpages></addata></record> |
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subjects | Arginine kinase Creatine kinase Exon/intron organization Gene Phosphagen kinase |
title | Evolution of the arginine kinase gene family |
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