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Isolation and characterization of cDNAs that encode eleven small GTP-binding proteins from Pisum sativum
Eleven cDNA clones (pral to pra9A, pra9B, and pra9C) were isolated from a pea (Pisum sativum) leaf cDNA library which were similar to small GTP-binding proteins. These cDNAs encoded proteins of 22–25 kDa, which exhibited 45–92% identity to one another at the amino acid level. The putative proteins i...
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Published in: | Plant and cell physiology 1993-04, Vol.34 (3), p.447-455 |
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creator | Nagano, Y. (Kyoto Univ. (Japan). Coll. of Agriculture) Murai, N Matsuno, R Sasaki, Y |
description | Eleven cDNA clones (pral to pra9A, pra9B, and pra9C) were isolated from a pea (Pisum sativum) leaf cDNA library which were similar to small GTP-binding proteins. These cDNAs encoded proteins of 22–25 kDa, which exhibited 45–92% identity to one another at the amino acid level. The putative proteins included the characteristic sequences of ras-related small GTP-binding proteins: four conserved domains involved in binding of GTP/GDP; an effector domain; and cysteine residues at the COOH-terminus. Indeed, the pra6 protein, expressed in Escherichia coli, clearly showed GTP-binding activity. Phylogenetic analysis showed that these clones can be classified into two subgroups: proteins encoded by pra1 to pra7 being related to ypt3 and rabll proteins; and proteins encoded by pra8, pra9A, pra9B, and pra9C being related to YPT1 and rab1 proteins. The effector sequences in these two subgroups were different. RNA gel blot analysis showed that most of the corresponding genes are differentially expressed in pea leaves and roots. Variations in expression were also observed for structurally related genes. |
doi_str_mv | 10.1093/oxfordjournals.pcp.a078439 |
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(Kyoto Univ. (Japan). Coll. of Agriculture) ; Murai, N ; Matsuno, R ; Sasaki, Y</creator><creatorcontrib>Nagano, Y. (Kyoto Univ. (Japan). Coll. of Agriculture) ; Murai, N ; Matsuno, R ; Sasaki, Y</creatorcontrib><description>Eleven cDNA clones (pral to pra9A, pra9B, and pra9C) were isolated from a pea (Pisum sativum) leaf cDNA library which were similar to small GTP-binding proteins. These cDNAs encoded proteins of 22–25 kDa, which exhibited 45–92% identity to one another at the amino acid level. The putative proteins included the characteristic sequences of ras-related small GTP-binding proteins: four conserved domains involved in binding of GTP/GDP; an effector domain; and cysteine residues at the COOH-terminus. Indeed, the pra6 protein, expressed in Escherichia coli, clearly showed GTP-binding activity. Phylogenetic analysis showed that these clones can be classified into two subgroups: proteins encoded by pra1 to pra7 being related to ypt3 and rabll proteins; and proteins encoded by pra8, pra9A, pra9B, and pra9C being related to YPT1 and rab1 proteins. The effector sequences in these two subgroups were different. RNA gel blot analysis showed that most of the corresponding genes are differentially expressed in pea leaves and roots. Variations in expression were also observed for structurally related genes.</description><identifier>ISSN: 0032-0781</identifier><identifier>ISSN: 1471-9053</identifier><identifier>EISSN: 1471-9053</identifier><identifier>DOI: 10.1093/oxfordjournals.pcp.a078439</identifier><identifier>PMID: 8019783</identifier><identifier>CODEN: PCPHA5</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>ADN ; Amino Acid Sequence ; ANALYTICAL METHODS ; Analytical, structural and metabolic biochemistry ; Binding and carrier proteins ; Biological and medical sciences ; Cell biochemistry ; Cell physiology ; Cloning, Molecular ; CODE GENETIQUE ; CODIGO GENETICO ; Conserved Sequence ; DNA ; DNA, Complementary - chemistry ; DNA, Complementary - isolation & purification ; Escherichia coli ; Fabaceae - genetics ; Fabaceae - metabolism ; Fundamental and applied biological sciences. Psychology ; GENETIC CODE ; GTP-binding proteins ; GTP-Binding Proteins - biosynthesis ; GTP-Binding Proteins - metabolism ; Molecular Sequence Data ; NUCLEOTIDE ; NUCLEOTIDES ; NUCLEOTIDOS ; Phylogeny ; PISUM SATIVUM ; Plant physiology and development ; Plants, Medicinal ; PROTEINAS ; PROTEINE ; PROTEINS ; Ras-related gene ; Sequence Homology, Amino Acid ; TECHNIQUE ANALYTIQUE ; TECNICAS ANALITICAS</subject><ispartof>Plant and cell physiology, 1993-04, Vol.34 (3), p.447-455</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27900,27901</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4804689$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8019783$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagano, Y. (Kyoto Univ. (Japan). Coll. of Agriculture)</creatorcontrib><creatorcontrib>Murai, N</creatorcontrib><creatorcontrib>Matsuno, R</creatorcontrib><creatorcontrib>Sasaki, Y</creatorcontrib><title>Isolation and characterization of cDNAs that encode eleven small GTP-binding proteins from Pisum sativum</title><title>Plant and cell physiology</title><addtitle>Plant Cell Physiol</addtitle><description>Eleven cDNA clones (pral to pra9A, pra9B, and pra9C) were isolated from a pea (Pisum sativum) leaf cDNA library which were similar to small GTP-binding proteins. These cDNAs encoded proteins of 22–25 kDa, which exhibited 45–92% identity to one another at the amino acid level. The putative proteins included the characteristic sequences of ras-related small GTP-binding proteins: four conserved domains involved in binding of GTP/GDP; an effector domain; and cysteine residues at the COOH-terminus. Indeed, the pra6 protein, expressed in Escherichia coli, clearly showed GTP-binding activity. Phylogenetic analysis showed that these clones can be classified into two subgroups: proteins encoded by pra1 to pra7 being related to ypt3 and rabll proteins; and proteins encoded by pra8, pra9A, pra9B, and pra9C being related to YPT1 and rab1 proteins. The effector sequences in these two subgroups were different. RNA gel blot analysis showed that most of the corresponding genes are differentially expressed in pea leaves and roots. Variations in expression were also observed for structurally related genes.</description><subject>ADN</subject><subject>Amino Acid Sequence</subject><subject>ANALYTICAL METHODS</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Binding and carrier proteins</subject><subject>Biological and medical sciences</subject><subject>Cell biochemistry</subject><subject>Cell physiology</subject><subject>Cloning, Molecular</subject><subject>CODE GENETIQUE</subject><subject>CODIGO GENETICO</subject><subject>Conserved Sequence</subject><subject>DNA</subject><subject>DNA, Complementary - chemistry</subject><subject>DNA, Complementary - isolation & purification</subject><subject>Escherichia coli</subject><subject>Fabaceae - genetics</subject><subject>Fabaceae - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GENETIC CODE</subject><subject>GTP-binding proteins</subject><subject>GTP-Binding Proteins - biosynthesis</subject><subject>GTP-Binding Proteins - metabolism</subject><subject>Molecular Sequence Data</subject><subject>NUCLEOTIDE</subject><subject>NUCLEOTIDES</subject><subject>NUCLEOTIDOS</subject><subject>Phylogeny</subject><subject>PISUM SATIVUM</subject><subject>Plant physiology and development</subject><subject>Plants, Medicinal</subject><subject>PROTEINAS</subject><subject>PROTEINE</subject><subject>PROTEINS</subject><subject>Ras-related gene</subject><subject>Sequence Homology, Amino Acid</subject><subject>TECHNIQUE ANALYTIQUE</subject><subject>TECNICAS ANALITICAS</subject><issn>0032-0781</issn><issn>1471-9053</issn><issn>1471-9053</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNqFkU9v1DAQxS0EKkvhCyAhWQhxy2LHjhNzqwpsiwosUvkjLtbEGXdTknixk6rw6XGVaCVOnGY07zfPIz9CnnO25kyLV_7W-dBc-ykM0MX13u7XwMpKCn2PrLgseaZZIe6TFWMiz5LCH5JHMV4zlnrBjshRxbhO7YrszqPvYGz9QGFoqN1BADtiaP_MQ--offPxJNJxByPFwfoGKXZ4gwONPXQd3Vxus7odmna4ovvgR2yHSF3wPd22ceppTEY3U_-YPHDpWHyy1GPy5d3by9Oz7OLT5vz05CKzeaXHLHcu10zyumigQl2JssC6kVjV3CKCzaUCi1pZzYVTAkApx1AUaBtRoivEMXk5-6Zbfk0YR9O30WLXwYB-iqZUuZZciv-CXJWykrlM4OsZtMHHGNCZfWh7CL8NZ-YuD_NvHiblYZY80vKz5ZWp7rE5rC4BJP3FokO00LkAg23jAZMVk6q6s8lmrI0j3h5kCD-NKtMfmbPvP8w39mG7yb9-NirxT2fegTdwFZLl-60uGFeKib8qbbOK</recordid><startdate>199304</startdate><enddate>199304</enddate><creator>Nagano, Y. 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Coll. of Agriculture) ; Murai, N ; Matsuno, R ; Sasaki, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c289t-2ff29041b5da8e98375ebd4e8b1ceeac246ace96c913f63aa66f0e35ecd37ef53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>ADN</topic><topic>Amino Acid Sequence</topic><topic>ANALYTICAL METHODS</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Binding and carrier proteins</topic><topic>Biological and medical sciences</topic><topic>Cell biochemistry</topic><topic>Cell physiology</topic><topic>Cloning, Molecular</topic><topic>CODE GENETIQUE</topic><topic>CODIGO GENETICO</topic><topic>Conserved Sequence</topic><topic>DNA</topic><topic>DNA, Complementary - chemistry</topic><topic>DNA, Complementary - isolation & purification</topic><topic>Escherichia coli</topic><topic>Fabaceae - genetics</topic><topic>Fabaceae - metabolism</topic><topic>Fundamental and applied biological sciences. 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Coll. of Agriculture)</creatorcontrib><creatorcontrib>Murai, N</creatorcontrib><creatorcontrib>Matsuno, R</creatorcontrib><creatorcontrib>Sasaki, Y</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Plant and cell physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagano, Y. (Kyoto Univ. (Japan). Coll. of Agriculture)</au><au>Murai, N</au><au>Matsuno, R</au><au>Sasaki, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation and characterization of cDNAs that encode eleven small GTP-binding proteins from Pisum sativum</atitle><jtitle>Plant and cell physiology</jtitle><addtitle>Plant Cell Physiol</addtitle><date>1993-04</date><risdate>1993</risdate><volume>34</volume><issue>3</issue><spage>447</spage><epage>455</epage><pages>447-455</pages><issn>0032-0781</issn><issn>1471-9053</issn><eissn>1471-9053</eissn><coden>PCPHA5</coden><abstract>Eleven cDNA clones (pral to pra9A, pra9B, and pra9C) were isolated from a pea (Pisum sativum) leaf cDNA library which were similar to small GTP-binding proteins. These cDNAs encoded proteins of 22–25 kDa, which exhibited 45–92% identity to one another at the amino acid level. The putative proteins included the characteristic sequences of ras-related small GTP-binding proteins: four conserved domains involved in binding of GTP/GDP; an effector domain; and cysteine residues at the COOH-terminus. Indeed, the pra6 protein, expressed in Escherichia coli, clearly showed GTP-binding activity. Phylogenetic analysis showed that these clones can be classified into two subgroups: proteins encoded by pra1 to pra7 being related to ypt3 and rabll proteins; and proteins encoded by pra8, pra9A, pra9B, and pra9C being related to YPT1 and rab1 proteins. The effector sequences in these two subgroups were different. RNA gel blot analysis showed that most of the corresponding genes are differentially expressed in pea leaves and roots. Variations in expression were also observed for structurally related genes.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>8019783</pmid><doi>10.1093/oxfordjournals.pcp.a078439</doi><tpages>9</tpages></addata></record> |
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subjects | ADN Amino Acid Sequence ANALYTICAL METHODS Analytical, structural and metabolic biochemistry Binding and carrier proteins Biological and medical sciences Cell biochemistry Cell physiology Cloning, Molecular CODE GENETIQUE CODIGO GENETICO Conserved Sequence DNA DNA, Complementary - chemistry DNA, Complementary - isolation & purification Escherichia coli Fabaceae - genetics Fabaceae - metabolism Fundamental and applied biological sciences. Psychology GENETIC CODE GTP-binding proteins GTP-Binding Proteins - biosynthesis GTP-Binding Proteins - metabolism Molecular Sequence Data NUCLEOTIDE NUCLEOTIDES NUCLEOTIDOS Phylogeny PISUM SATIVUM Plant physiology and development Plants, Medicinal PROTEINAS PROTEINE PROTEINS Ras-related gene Sequence Homology, Amino Acid TECHNIQUE ANALYTIQUE TECNICAS ANALITICAS |
title | Isolation and characterization of cDNAs that encode eleven small GTP-binding proteins from Pisum sativum |
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