Selection of Arabidopsis genes encoding secreted and plasma membrane proteins
Secreted and plasma membrane proteins play crucial roles in a variety of physiological and developmental processes of multicellular organisms. Systematic cloning of the genes encoding these proteins is therefore of general interest. An effective method of trapping signal sequences was first describe...
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Veröffentlicht in: | Plant molecular biology 1999-10, Vol.41 (3), p.415-423 |
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description | Secreted and plasma membrane proteins play crucial roles in a variety of physiological and developmental processes of multicellular organisms. Systematic cloning of the genes encoding these proteins is therefore of general interest. An effective method of trapping signal sequences was first described by Tashiro et al. (1993), and a similar yet more efficient method was reported by Klein et al. (1996) and Jacobs et al. (1997). In this study, we carried out the latter yeast-based signal sequence trap to clone genes from Arabidopsis thaliana encoding secreted and plasma membrane proteins. Of 144 sequenced cDNA clones, 18% are identical to previously cloned Arabidopsis thaliana genes, 12% are homologous to genes identified from various organisms, and 46% are novel. All of the isolated genes identical or homologous to previously reported genes are either secreted or plasma membrane proteins, and the remaining novel genes appear to contain functional signal sequences based on computer-aided sequence analysis. The full-length cDNA clones of one homologous gene and another novel gene were isolated and sequenced. The deduced amino acid sequences suggest that the former encodes a secreted protein, and the latter encodes a type 1 membrane protein. These results indicate that the signal sequence trap method is effective and useful for the isolation of plant genes encoding secreted and plasma membrane proteins. |
doi_str_mv | 10.1023/A:1006395724405 |
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Systematic cloning of the genes encoding these proteins is therefore of general interest. An effective method of trapping signal sequences was first described by Tashiro et al. (1993), and a similar yet more efficient method was reported by Klein et al. (1996) and Jacobs et al. (1997). In this study, we carried out the latter yeast-based signal sequence trap to clone genes from Arabidopsis thaliana encoding secreted and plasma membrane proteins. Of 144 sequenced cDNA clones, 18% are identical to previously cloned Arabidopsis thaliana genes, 12% are homologous to genes identified from various organisms, and 46% are novel. All of the isolated genes identical or homologous to previously reported genes are either secreted or plasma membrane proteins, and the remaining novel genes appear to contain functional signal sequences based on computer-aided sequence analysis. The full-length cDNA clones of one homologous gene and another novel gene were isolated and sequenced. The deduced amino acid sequences suggest that the former encodes a secreted protein, and the latter encodes a type 1 membrane protein. These results indicate that the signal sequence trap method is effective and useful for the isolation of plant genes encoding secreted and plasma membrane proteins.</description><identifier>ISSN: 0167-4412</identifier><identifier>EISSN: 1573-5028</identifier><identifier>DOI: 10.1023/A:1006395724405</identifier><identifier>PMID: 10598107</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Amino Acid Sequence ; amino acid sequences ; Amino acids ; Arabidopsis - genetics ; Arabidopsis thaliana ; biochemical techniques ; Cell Membrane - genetics ; Cellular biology ; Cloning ; complementary DNA ; DNA, Complementary - genetics ; genbank/af104328 ; genbank/af104329 ; gene expression ; Gene Library ; genes ; Genes, Plant ; genetic transformation ; Membrane Proteins - genetics ; Membranes ; Molecular Sequence Data ; nucleotide sequences ; plant proteins ; Plant Proteins - metabolism ; Plasma ; plasma membrane ; protein secretion ; Protein Sorting Signals - genetics ; Proteins ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; screening ; Sequence Analysis, DNA ; Sequence Homology, Amino Acid ; signal peptide ; signal sequence trap methods ; Yeasts</subject><ispartof>Plant molecular biology, 1999-10, Vol.41 (3), p.415-423</ispartof><rights>Kluwer Academic Publishers 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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/10598107$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goo, J.H</creatorcontrib><creatorcontrib>Park, A.R</creatorcontrib><creatorcontrib>Park, W.J</creatorcontrib><creatorcontrib>Park, O.K</creatorcontrib><title>Selection of Arabidopsis genes encoding secreted and plasma membrane proteins</title><title>Plant molecular biology</title><addtitle>Plant Mol Biol</addtitle><description>Secreted and plasma membrane proteins play crucial roles in a variety of physiological and developmental processes of multicellular organisms. Systematic cloning of the genes encoding these proteins is therefore of general interest. An effective method of trapping signal sequences was first described by Tashiro et al. (1993), and a similar yet more efficient method was reported by Klein et al. (1996) and Jacobs et al. (1997). In this study, we carried out the latter yeast-based signal sequence trap to clone genes from Arabidopsis thaliana encoding secreted and plasma membrane proteins. Of 144 sequenced cDNA clones, 18% are identical to previously cloned Arabidopsis thaliana genes, 12% are homologous to genes identified from various organisms, and 46% are novel. All of the isolated genes identical or homologous to previously reported genes are either secreted or plasma membrane proteins, and the remaining novel genes appear to contain functional signal sequences based on computer-aided sequence analysis. The full-length cDNA clones of one homologous gene and another novel gene were isolated and sequenced. The deduced amino acid sequences suggest that the former encodes a secreted protein, and the latter encodes a type 1 membrane protein. These results indicate that the signal sequence trap method is effective and useful for the isolation of plant genes encoding secreted and plasma membrane proteins.</description><subject>Amino Acid Sequence</subject><subject>amino acid sequences</subject><subject>Amino acids</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis thaliana</subject><subject>biochemical techniques</subject><subject>Cell Membrane - genetics</subject><subject>Cellular biology</subject><subject>Cloning</subject><subject>complementary DNA</subject><subject>DNA, Complementary - genetics</subject><subject>genbank/af104328</subject><subject>genbank/af104329</subject><subject>gene expression</subject><subject>Gene Library</subject><subject>genes</subject><subject>Genes, Plant</subject><subject>genetic transformation</subject><subject>Membrane Proteins - genetics</subject><subject>Membranes</subject><subject>Molecular Sequence Data</subject><subject>nucleotide sequences</subject><subject>plant proteins</subject><subject>Plant Proteins - metabolism</subject><subject>Plasma</subject><subject>plasma membrane</subject><subject>protein secretion</subject><subject>Protein Sorting Signals - genetics</subject><subject>Proteins</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>screening</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Homology, Amino Acid</subject><subject>signal peptide</subject><subject>signal sequence trap methods</subject><subject>Yeasts</subject><issn>0167-4412</issn><issn>1573-5028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqF0TlPwzAUB3ALgWgpzGxgMbAFfB9sVcUlFTGUztFL7FSpkrjEycC3x6hlYWF6y0_v-D-ELim5o4Tx-_kDJURxKzUTgsgjNKVS80wSZo7RlFClMyEom6CzGLeEJMzVKZpQIq2hRE_R28o3vhzq0OFQ4XkPRe3CLtYRb3znI_ZdGVzdbXD0Ze8H7zB0Du8aiC3g1rdFD53Huz4Mvu7iOTqpoIn-4lBnaP30-LF4yZbvz6-L-TKrmLFDVoAWylimpFGKS6Yrpy0YgIJapxgRFXEKoFRWGFpJbp3khjKnCoBK6ILP0O2-bxr8Ofo45G0dS980aZkwxlxZLqUm5l9ItZA_ySV48wduw9h36YhcayqkopImdHVAY9F6l-_6uoX-K_-NM4HrPagg5LDp65ivV4xQTlh6kRWKfwMwgX60</recordid><startdate>19991001</startdate><enddate>19991001</enddate><creator>Goo, J.H</creator><creator>Park, A.R</creator><creator>Park, W.J</creator><creator>Park, O.K</creator><general>Springer Nature B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19991001</creationdate><title>Selection of Arabidopsis genes encoding secreted and plasma membrane proteins</title><author>Goo, J.H ; Park, A.R ; Park, W.J ; Park, O.K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f289t-ba746892658663527fd79a8aab19d6204f0d6aac69481f539d53812d6baaf47b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Amino Acid Sequence</topic><topic>amino acid sequences</topic><topic>Amino acids</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis thaliana</topic><topic>biochemical techniques</topic><topic>Cell Membrane - genetics</topic><topic>Cellular biology</topic><topic>Cloning</topic><topic>complementary DNA</topic><topic>DNA, Complementary - genetics</topic><topic>genbank/af104328</topic><topic>genbank/af104329</topic><topic>gene expression</topic><topic>Gene Library</topic><topic>genes</topic><topic>Genes, Plant</topic><topic>genetic transformation</topic><topic>Membrane Proteins - genetics</topic><topic>Membranes</topic><topic>Molecular Sequence Data</topic><topic>nucleotide sequences</topic><topic>plant proteins</topic><topic>Plant Proteins - metabolism</topic><topic>Plasma</topic><topic>plasma membrane</topic><topic>protein secretion</topic><topic>Protein Sorting Signals - genetics</topic><topic>Proteins</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>screening</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Homology, Amino Acid</topic><topic>signal peptide</topic><topic>signal sequence trap methods</topic><topic>Yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goo, J.H</creatorcontrib><creatorcontrib>Park, A.R</creatorcontrib><creatorcontrib>Park, W.J</creatorcontrib><creatorcontrib>Park, O.K</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Plant molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goo, J.H</au><au>Park, A.R</au><au>Park, W.J</au><au>Park, O.K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selection of Arabidopsis genes encoding secreted and plasma membrane proteins</atitle><jtitle>Plant molecular biology</jtitle><addtitle>Plant Mol Biol</addtitle><date>1999-10-01</date><risdate>1999</risdate><volume>41</volume><issue>3</issue><spage>415</spage><epage>423</epage><pages>415-423</pages><issn>0167-4412</issn><eissn>1573-5028</eissn><abstract>Secreted and plasma membrane proteins play crucial roles in a variety of physiological and developmental processes of multicellular organisms. Systematic cloning of the genes encoding these proteins is therefore of general interest. An effective method of trapping signal sequences was first described by Tashiro et al. (1993), and a similar yet more efficient method was reported by Klein et al. (1996) and Jacobs et al. (1997). In this study, we carried out the latter yeast-based signal sequence trap to clone genes from Arabidopsis thaliana encoding secreted and plasma membrane proteins. Of 144 sequenced cDNA clones, 18% are identical to previously cloned Arabidopsis thaliana genes, 12% are homologous to genes identified from various organisms, and 46% are novel. All of the isolated genes identical or homologous to previously reported genes are either secreted or plasma membrane proteins, and the remaining novel genes appear to contain functional signal sequences based on computer-aided sequence analysis. The full-length cDNA clones of one homologous gene and another novel gene were isolated and sequenced. The deduced amino acid sequences suggest that the former encodes a secreted protein, and the latter encodes a type 1 membrane protein. These results indicate that the signal sequence trap method is effective and useful for the isolation of plant genes encoding secreted and plasma membrane proteins.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>10598107</pmid><doi>10.1023/A:1006395724405</doi><tpages>9</tpages></addata></record> |
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subjects | Amino Acid Sequence amino acid sequences Amino acids Arabidopsis - genetics Arabidopsis thaliana biochemical techniques Cell Membrane - genetics Cellular biology Cloning complementary DNA DNA, Complementary - genetics genbank/af104328 genbank/af104329 gene expression Gene Library genes Genes, Plant genetic transformation Membrane Proteins - genetics Membranes Molecular Sequence Data nucleotide sequences plant proteins Plant Proteins - metabolism Plasma plasma membrane protein secretion Protein Sorting Signals - genetics Proteins Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics screening Sequence Analysis, DNA Sequence Homology, Amino Acid signal peptide signal sequence trap methods Yeasts |
title | Selection of Arabidopsis genes encoding secreted and plasma membrane proteins |
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