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The unconventional myosin encoded by the myoA gene plays a role in Dictyostelium motility
The myoA gene of Dictyostelium is a member of a gene family of unconventional myosins. The myosin Is share homologous head and basic domains, but the myoA gene product lacks the glycine-, proline-, alanine-rich and src homology 3 domains typical of several of the other myosin Is. A mutant strain of...
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Published in: | Molecular biology of the cell 1993-02, Vol.4 (2), p.233-246 |
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description | The myoA gene of Dictyostelium is a member of a gene family of unconventional myosins. The myosin Is share homologous head and basic domains, but the myoA gene product lacks the glycine-, proline-, alanine-rich and src homology 3 domains typical of several of the other myosin Is. A mutant strain of Dictyostelium lacking a functional myoA gene was produced by gene targeting, and the motility of this strain in buffer and a spatial gradient of the chemoattractant cyclic AMP was analyzed by computer-assisted methods. The myoA- cells have a normal elongate morphology in buffer but exhibit a decrease in the instantaneous velocity of cellular translocation, an increase in the frequency of lateral pseudopod formation, and an increase in turning. In a spatial gradient, in which the frequency of pseudopod formation is depressed, myoA- cells exhibit positive chemotaxis but still turn several times more frequently than control cells. These results demonstrate that the other members of the unconventional myosin family do not fully compensate for the loss of functional myoA gene product. Surprisingly, the phenotype of the myoA- strain closely resembles that of the myoB- strain, suggesting that both play a role in the frequency of pseudopod formation and turning during cellular translocation. |
doi_str_mv | 10.1091/mbc.4.2.233 |
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In a spatial gradient, in which the frequency of pseudopod formation is depressed, myoA- cells exhibit positive chemotaxis but still turn several times more frequently than control cells. These results demonstrate that the other members of the unconventional myosin family do not fully compensate for the loss of functional myoA gene product. Surprisingly, the phenotype of the myoA- strain closely resembles that of the myoB- strain, suggesting that both play a role in the frequency of pseudopod formation and turning during cellular translocation.</description><identifier>ISSN: 1059-1524</identifier><identifier>EISSN: 1939-4586</identifier><identifier>DOI: 10.1091/mbc.4.2.233</identifier><identifier>PMID: 8382977</identifier><language>eng</language><publisher>Bethesda, MD: American Society for Cell Biology</publisher><subject>Animals ; Base Sequence ; Biological and medical sciences ; Cell Movement ; Chemotaxis ; Classical genetics, quantitative genetics, hybrids ; Cyclic AMP - physiology ; Dictyostelium - genetics ; Dictyostelium - physiology ; DNA, Fungal - genetics ; Fundamental and applied biological sciences. Psychology ; Gene Expression ; Genes, Fungal ; Genetics of eukaryotes. 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A</creatorcontrib><creatorcontrib>WESSELS, D</creatorcontrib><creatorcontrib>SPUDICH, J. A</creatorcontrib><creatorcontrib>SOLL, D</creatorcontrib><title>The unconventional myosin encoded by the myoA gene plays a role in Dictyostelium motility</title><title>Molecular biology of the cell</title><addtitle>Mol Biol Cell</addtitle><description>The myoA gene of Dictyostelium is a member of a gene family of unconventional myosins. The myosin Is share homologous head and basic domains, but the myoA gene product lacks the glycine-, proline-, alanine-rich and src homology 3 domains typical of several of the other myosin Is. A mutant strain of Dictyostelium lacking a functional myoA gene was produced by gene targeting, and the motility of this strain in buffer and a spatial gradient of the chemoattractant cyclic AMP was analyzed by computer-assisted methods. The myoA- cells have a normal elongate morphology in buffer but exhibit a decrease in the instantaneous velocity of cellular translocation, an increase in the frequency of lateral pseudopod formation, and an increase in turning. In a spatial gradient, in which the frequency of pseudopod formation is depressed, myoA- cells exhibit positive chemotaxis but still turn several times more frequently than control cells. These results demonstrate that the other members of the unconventional myosin family do not fully compensate for the loss of functional myoA gene product. Surprisingly, the phenotype of the myoA- strain closely resembles that of the myoB- strain, suggesting that both play a role in the frequency of pseudopod formation and turning during cellular translocation.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Cell Movement</subject><subject>Chemotaxis</subject><subject>Classical genetics, quantitative genetics, hybrids</subject><subject>Cyclic AMP - physiology</subject><subject>Dictyostelium - genetics</subject><subject>Dictyostelium - physiology</subject><subject>DNA, Fungal - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression</subject><subject>Genes, Fungal</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Molecular Sequence Data</subject><subject>Mutagenesis, Insertional</subject><subject>Myosins - genetics</subject><subject>Myosins - physiology</subject><subject>Oligodeoxyribonucleotides - chemistry</subject><subject>Protozoa</subject><subject>RNA, Fungal - genetics</subject><subject>RNA, Messenger - genetics</subject><issn>1059-1524</issn><issn>1939-4586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNpVkM1LwzAYh4Moc05PnoUcvElrvtomBw8yP2HgZR48hSRNt0iajqYb9L83sjH0lPD-nl_C-wBwjVGOkcD3rTY5y0lOKD0BUyyoyFjBy9N0R4XIcEHYObiI8RshzFhZTcCEU05EVU3B13Jt4TaYLuxsGFwXlIft2EUXoE3T2tZQj3BIUJo-wpUNFm68GiNUsO-8hQl8cmZIlcF6t21h2w3Ou2G8BGeN8tFeHc4Z-Hx5Xs7fssXH6_v8cZEZVqEhqyjjVldKI4KZLilXgmlVEEGMVY2g2BijTUkLbHjRcIyM1WkhXlvMjdCWzsDD_t3NVre2NmmNXnm56V2r-lF2ysn_SXBruep2kqIkj6f-3b5v-i7G3jbHKkby169MfiWTRCa_ib75-9uRPQhN-e0hV9Eo3_QqGBePGCsTWDD6A-2Ahh0</recordid><startdate>19930201</startdate><enddate>19930201</enddate><creator>TITUS, M. A</creator><creator>WESSELS, D</creator><creator>SPUDICH, J. A</creator><creator>SOLL, D</creator><general>American Society for Cell Biology</general><scope>IQODW</scope><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>5PM</scope></search><sort><creationdate>19930201</creationdate><title>The unconventional myosin encoded by the myoA gene plays a role in Dictyostelium motility</title><author>TITUS, M. A ; WESSELS, D ; SPUDICH, J. A ; SOLL, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-7348eb7ab0214b638a94ba5292ceaf931cccbc6351c85f810ceb5248de18c9be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Cell Movement</topic><topic>Chemotaxis</topic><topic>Classical genetics, quantitative genetics, hybrids</topic><topic>Cyclic AMP - physiology</topic><topic>Dictyostelium - genetics</topic><topic>Dictyostelium - physiology</topic><topic>DNA, Fungal - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression</topic><topic>Genes, Fungal</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Molecular Sequence Data</topic><topic>Mutagenesis, Insertional</topic><topic>Myosins - genetics</topic><topic>Myosins - physiology</topic><topic>Oligodeoxyribonucleotides - chemistry</topic><topic>Protozoa</topic><topic>RNA, Fungal - genetics</topic><topic>RNA, Messenger - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TITUS, M. A</creatorcontrib><creatorcontrib>WESSELS, D</creatorcontrib><creatorcontrib>SPUDICH, J. A</creatorcontrib><creatorcontrib>SOLL, D</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular biology of the cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TITUS, M. A</au><au>WESSELS, D</au><au>SPUDICH, J. A</au><au>SOLL, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The unconventional myosin encoded by the myoA gene plays a role in Dictyostelium motility</atitle><jtitle>Molecular biology of the cell</jtitle><addtitle>Mol Biol Cell</addtitle><date>1993-02-01</date><risdate>1993</risdate><volume>4</volume><issue>2</issue><spage>233</spage><epage>246</epage><pages>233-246</pages><issn>1059-1524</issn><eissn>1939-4586</eissn><abstract>The myoA gene of Dictyostelium is a member of a gene family of unconventional myosins. The myosin Is share homologous head and basic domains, but the myoA gene product lacks the glycine-, proline-, alanine-rich and src homology 3 domains typical of several of the other myosin Is. A mutant strain of Dictyostelium lacking a functional myoA gene was produced by gene targeting, and the motility of this strain in buffer and a spatial gradient of the chemoattractant cyclic AMP was analyzed by computer-assisted methods. The myoA- cells have a normal elongate morphology in buffer but exhibit a decrease in the instantaneous velocity of cellular translocation, an increase in the frequency of lateral pseudopod formation, and an increase in turning. In a spatial gradient, in which the frequency of pseudopod formation is depressed, myoA- cells exhibit positive chemotaxis but still turn several times more frequently than control cells. These results demonstrate that the other members of the unconventional myosin family do not fully compensate for the loss of functional myoA gene product. Surprisingly, the phenotype of the myoA- strain closely resembles that of the myoB- strain, suggesting that both play a role in the frequency of pseudopod formation and turning during cellular translocation.</abstract><cop>Bethesda, MD</cop><pub>American Society for Cell Biology</pub><pmid>8382977</pmid><doi>10.1091/mbc.4.2.233</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Base Sequence Biological and medical sciences Cell Movement Chemotaxis Classical genetics, quantitative genetics, hybrids Cyclic AMP - physiology Dictyostelium - genetics Dictyostelium - physiology DNA, Fungal - genetics Fundamental and applied biological sciences. Psychology Gene Expression Genes, Fungal Genetics of eukaryotes. Biological and molecular evolution Molecular Sequence Data Mutagenesis, Insertional Myosins - genetics Myosins - physiology Oligodeoxyribonucleotides - chemistry Protozoa RNA, Fungal - genetics RNA, Messenger - genetics |
title | The unconventional myosin encoded by the myoA gene plays a role in Dictyostelium motility |
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