Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Molecular biology of the cell 1993-02, Vol.4 (2), p.233-246
Main Authors: TITUS, M. A, WESSELS, D, SPUDICH, J. A, SOLL, D
Format: Article
Language:English
Subjects:
Citations: 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-c470t-7348eb7ab0214b638a94ba5292ceaf931cccbc6351c85f810ceb5248de18c9be3
cites
container_end_page 246
container_issue 2
container_start_page 233
container_title Molecular biology of the cell
container_volume 4
creator TITUS, M. A
WESSELS, D
SPUDICH, J. A
SOLL, D
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
format article
fullrecord <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_300918</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>8382977</sourcerecordid><originalsourceid>FETCH-LOGICAL-c470t-7348eb7ab0214b638a94ba5292ceaf931cccbc6351c85f810ceb5248de18c9be3</originalsourceid><addsrcrecordid>eNpVkM1LwzAYh4Moc05PnoUcvElrvtomBw8yP2HgZR48hSRNt0iajqYb9L83sjH0lPD-nl_C-wBwjVGOkcD3rTY5y0lOKD0BUyyoyFjBy9N0R4XIcEHYObiI8RshzFhZTcCEU05EVU3B13Jt4TaYLuxsGFwXlIft2EUXoE3T2tZQj3BIUJo-wpUNFm68GiNUsO-8hQl8cmZIlcF6t21h2w3Ou2G8BGeN8tFeHc4Z-Hx5Xs7fssXH6_v8cZEZVqEhqyjjVldKI4KZLilXgmlVEEGMVY2g2BijTUkLbHjRcIyM1WkhXlvMjdCWzsDD_t3NVre2NmmNXnm56V2r-lF2ysn_SXBruep2kqIkj6f-3b5v-i7G3jbHKkby169MfiWTRCa_ib75-9uRPQhN-e0hV9Eo3_QqGBePGCsTWDD6A-2Ahh0</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The unconventional myosin encoded by the myoA gene plays a role in Dictyostelium motility</title><source>PubMed Central</source><creator>TITUS, M. A ; WESSELS, D ; SPUDICH, J. A ; SOLL, D</creator><creatorcontrib>TITUS, M. A ; WESSELS, D ; SPUDICH, J. A ; SOLL, D</creatorcontrib><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><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. Biological and molecular evolution ; Molecular Sequence Data ; Mutagenesis, Insertional ; Myosins - genetics ; Myosins - physiology ; Oligodeoxyribonucleotides - chemistry ; Protozoa ; RNA, Fungal - genetics ; RNA, Messenger - genetics</subject><ispartof>Molecular biology of the cell, 1993-02, Vol.4 (2), p.233-246</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-7348eb7ab0214b638a94ba5292ceaf931cccbc6351c85f810ceb5248de18c9be3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC300918/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC300918/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4683854$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8382977$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TITUS, M. 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>
fulltext fulltext
identifier ISSN: 1059-1524
ispartof Molecular biology of the cell, 1993-02, Vol.4 (2), p.233-246
issn 1059-1524
1939-4586
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_300918
source PubMed Central
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T00%3A37%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20unconventional%20myosin%20encoded%20by%20the%20myoA%20gene%20plays%20a%20role%20in%20Dictyostelium%20motility&rft.jtitle=Molecular%20biology%20of%20the%20cell&rft.au=TITUS,%20M.%20A&rft.date=1993-02-01&rft.volume=4&rft.issue=2&rft.spage=233&rft.epage=246&rft.pages=233-246&rft.issn=1059-1524&rft.eissn=1939-4586&rft_id=info:doi/10.1091/mbc.4.2.233&rft_dat=%3Cpubmed_cross%3E8382977%3C/pubmed_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c470t-7348eb7ab0214b638a94ba5292ceaf931cccbc6351c85f810ceb5248de18c9be3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/8382977&rfr_iscdi=true