Loading…

Glutamine synthetase in the phloem plays a major role in controlling proline production

To inhibit expression specifically in the phloem, a 274-bp fragment of a cDNA (Gln1-5) encoding cytosolic glutamine synthetase (GS1) from tobacco was placed in the antisense orientation downstream of the cytosolic Cu/Zn superoxide dismutase promoter of Nicotiana plumbaginifolia. After Agrobacterium-...

Full description

Saved in:
Bibliographic Details
Published in:The Plant cell 1999-10, Vol.11 (10), p.1995-2011
Main Authors: Brugiere, N, Dubois, F, Limami, A.M, Lelandais, M, Roux, Y, Sangwan, R.S, Hirel, B
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-c447t-bab87f285256e73e18dfdaee92104f20b27d5b8028e03b18d1d72ead04ba4f333
cites
container_end_page 2011
container_issue 10
container_start_page 1995
container_title The Plant cell
container_volume 11
creator Brugiere, N
Dubois, F
Limami, A.M
Lelandais, M
Roux, Y
Sangwan, R.S
Hirel, B
description To inhibit expression specifically in the phloem, a 274-bp fragment of a cDNA (Gln1-5) encoding cytosolic glutamine synthetase (GS1) from tobacco was placed in the antisense orientation downstream of the cytosolic Cu/Zn superoxide dismutase promoter of Nicotiana plumbaginifolia. After Agrobacterium-mediated transformation, two transgenic N. tabacum lines exhibiting reduced levels of GS1 mRNA and GS activity in midribs, stems, and roots were obtained. Immunogold labeling experiments allowed us to verify that the GS protein content was markedly decreased in the phloem companion cells of transformed plants. Moreover, a general decrease in proline content in the transgenic plants in comparison with wild-type tobacco was observed when plants were forced to assimilate large amounts of ammonium. In contrast, no major changes in the concentration of amino acids used for nitrogen transport were apparent. A 15NH4(+)-labeling kinetic over a 48-hr period confirmed that in leaves of transgenic plants, the decrease in proline production was directly related to glutamine availability. After 2 weeks of salt treatment, the transgenic plants had a pronounced stress phenotype, consisting of wilting and bleaching in the older leaves. We conclude that GS in the phloem plays a major role in regulating proline production consistent with the function of proline as a nitrogen source and as a key metabolite synthesized in response to water stress.
doi_str_mv 10.1105/tpc.11.10.1995
format article
fullrecord <record><control><sourceid>jstor_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1859309388</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>3871093</jstor_id><sourcerecordid>3871093</sourcerecordid><originalsourceid>FETCH-LOGICAL-c447t-bab87f285256e73e18dfdaee92104f20b27d5b8028e03b18d1d72ead04ba4f333</originalsourceid><addsrcrecordid>eNpdkDtPwzAUhS0EoqWwMoKFGFhS_IhrZ0QVLwmJARBslpM4baokDrYz9N9z2zAgpnuu_N3jo4PQOSVzSom4jX0BYr5bs0wcoCkVnCUsU1-HoElKknQh6ASdhLAhhFBJs2M0gUtGBVNT9PnYDNG0dWdx2HZxbaMJFtcdBon7deNsi_vGbAM2uDUb57F3zR4oXBdBN3W3wj2InQXMcihi7bpTdFSZJtiz3zlDHw_378un5OX18Xl595IUaSpjkptcyYopwcTCSm6pKqvSWJsxyF4xkjNZilwRpizhObzSUjJrSpLmJq045zN0M_rC19-DDVG3dShs05jOuiFoqkTGScaVAvTqH7pxg-8gnWZUSakWXAI0H6HCuxC8rXTv69b4raZE7xrX0DiI_QqNw8HFr-uQt7b8g48VA3A9ApsQnf9rxziRmitJIR9glyNWGafNytdBf7wxQjlhmVhAPfwHMoqRQg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>218778637</pqid></control><display><type>article</type><title>Glutamine synthetase in the phloem plays a major role in controlling proline production</title><source>Oxford Journals Online</source><source>JSTOR Archival Journals</source><creator>Brugiere, N ; Dubois, F ; Limami, A.M ; Lelandais, M ; Roux, Y ; Sangwan, R.S ; Hirel, B</creator><creatorcontrib>Brugiere, N ; Dubois, F ; Limami, A.M ; Lelandais, M ; Roux, Y ; Sangwan, R.S ; Hirel, B</creatorcontrib><description>To inhibit expression specifically in the phloem, a 274-bp fragment of a cDNA (Gln1-5) encoding cytosolic glutamine synthetase (GS1) from tobacco was placed in the antisense orientation downstream of the cytosolic Cu/Zn superoxide dismutase promoter of Nicotiana plumbaginifolia. After Agrobacterium-mediated transformation, two transgenic N. tabacum lines exhibiting reduced levels of GS1 mRNA and GS activity in midribs, stems, and roots were obtained. Immunogold labeling experiments allowed us to verify that the GS protein content was markedly decreased in the phloem companion cells of transformed plants. Moreover, a general decrease in proline content in the transgenic plants in comparison with wild-type tobacco was observed when plants were forced to assimilate large amounts of ammonium. In contrast, no major changes in the concentration of amino acids used for nitrogen transport were apparent. A 15NH4(+)-labeling kinetic over a 48-hr period confirmed that in leaves of transgenic plants, the decrease in proline production was directly related to glutamine availability. After 2 weeks of salt treatment, the transgenic plants had a pronounced stress phenotype, consisting of wilting and bleaching in the older leaves. We conclude that GS in the phloem plays a major role in regulating proline production consistent with the function of proline as a nitrogen source and as a key metabolite synthesized in response to water stress.</description><identifier>ISSN: 1040-4651</identifier><identifier>EISSN: 1532-298X</identifier><identifier>DOI: 10.1105/tpc.11.10.1995</identifier><identifier>PMID: 10521528</identifier><language>eng</language><publisher>United States: American Society of Plant Physiologists</publisher><subject>Amino acids ; ammonium compounds ; antisense DNA ; chemical constituents of plants ; complementary DNA ; enzyme activity ; free amino acids ; gene expression ; glutamate-ammonia ligase ; immunocytochemistry ; Leaves ; messenger RNA ; Nicotiana plumbaginifolia ; Nicotiana tabacum ; Nitrogen ; nitrogen metabolism ; Phloem ; Phloem companion cells ; Plant cells ; Plant roots ; Plants ; proline ; promoter regions ; recombinant DNA ; roots ; salinity ; sodium chloride ; Stems ; stress ; superoxide dismutase ; Transgenic plants</subject><ispartof>The Plant cell, 1999-10, Vol.11 (10), p.1995-2011</ispartof><rights>Copyright 1999 American Society of Plant Physiologists</rights><rights>Copyright American Society of Plant Physiologists Oct 1999</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-bab87f285256e73e18dfdaee92104f20b27d5b8028e03b18d1d72ead04ba4f333</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3871093$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3871093$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,58213,58446</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10521528$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brugiere, N</creatorcontrib><creatorcontrib>Dubois, F</creatorcontrib><creatorcontrib>Limami, A.M</creatorcontrib><creatorcontrib>Lelandais, M</creatorcontrib><creatorcontrib>Roux, Y</creatorcontrib><creatorcontrib>Sangwan, R.S</creatorcontrib><creatorcontrib>Hirel, B</creatorcontrib><title>Glutamine synthetase in the phloem plays a major role in controlling proline production</title><title>The Plant cell</title><addtitle>Plant Cell</addtitle><description>To inhibit expression specifically in the phloem, a 274-bp fragment of a cDNA (Gln1-5) encoding cytosolic glutamine synthetase (GS1) from tobacco was placed in the antisense orientation downstream of the cytosolic Cu/Zn superoxide dismutase promoter of Nicotiana plumbaginifolia. After Agrobacterium-mediated transformation, two transgenic N. tabacum lines exhibiting reduced levels of GS1 mRNA and GS activity in midribs, stems, and roots were obtained. Immunogold labeling experiments allowed us to verify that the GS protein content was markedly decreased in the phloem companion cells of transformed plants. Moreover, a general decrease in proline content in the transgenic plants in comparison with wild-type tobacco was observed when plants were forced to assimilate large amounts of ammonium. In contrast, no major changes in the concentration of amino acids used for nitrogen transport were apparent. A 15NH4(+)-labeling kinetic over a 48-hr period confirmed that in leaves of transgenic plants, the decrease in proline production was directly related to glutamine availability. After 2 weeks of salt treatment, the transgenic plants had a pronounced stress phenotype, consisting of wilting and bleaching in the older leaves. We conclude that GS in the phloem plays a major role in regulating proline production consistent with the function of proline as a nitrogen source and as a key metabolite synthesized in response to water stress.</description><subject>Amino acids</subject><subject>ammonium compounds</subject><subject>antisense DNA</subject><subject>chemical constituents of plants</subject><subject>complementary DNA</subject><subject>enzyme activity</subject><subject>free amino acids</subject><subject>gene expression</subject><subject>glutamate-ammonia ligase</subject><subject>immunocytochemistry</subject><subject>Leaves</subject><subject>messenger RNA</subject><subject>Nicotiana plumbaginifolia</subject><subject>Nicotiana tabacum</subject><subject>Nitrogen</subject><subject>nitrogen metabolism</subject><subject>Phloem</subject><subject>Phloem companion cells</subject><subject>Plant cells</subject><subject>Plant roots</subject><subject>Plants</subject><subject>proline</subject><subject>promoter regions</subject><subject>recombinant DNA</subject><subject>roots</subject><subject>salinity</subject><subject>sodium chloride</subject><subject>Stems</subject><subject>stress</subject><subject>superoxide dismutase</subject><subject>Transgenic plants</subject><issn>1040-4651</issn><issn>1532-298X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNpdkDtPwzAUhS0EoqWwMoKFGFhS_IhrZ0QVLwmJARBslpM4baokDrYz9N9z2zAgpnuu_N3jo4PQOSVzSom4jX0BYr5bs0wcoCkVnCUsU1-HoElKknQh6ASdhLAhhFBJs2M0gUtGBVNT9PnYDNG0dWdx2HZxbaMJFtcdBon7deNsi_vGbAM2uDUb57F3zR4oXBdBN3W3wj2InQXMcihi7bpTdFSZJtiz3zlDHw_378un5OX18Xl595IUaSpjkptcyYopwcTCSm6pKqvSWJsxyF4xkjNZilwRpizhObzSUjJrSpLmJq045zN0M_rC19-DDVG3dShs05jOuiFoqkTGScaVAvTqH7pxg-8gnWZUSakWXAI0H6HCuxC8rXTv69b4raZE7xrX0DiI_QqNw8HFr-uQt7b8g48VA3A9ApsQnf9rxziRmitJIR9glyNWGafNytdBf7wxQjlhmVhAPfwHMoqRQg</recordid><startdate>19991001</startdate><enddate>19991001</enddate><creator>Brugiere, N</creator><creator>Dubois, F</creator><creator>Limami, A.M</creator><creator>Lelandais, M</creator><creator>Roux, Y</creator><creator>Sangwan, R.S</creator><creator>Hirel, B</creator><general>American Society of Plant Physiologists</general><general>American Society of Plant Biologists</general><scope>FBQ</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>7QO</scope><scope>7TM</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</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>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>19991001</creationdate><title>Glutamine synthetase in the phloem plays a major role in controlling proline production</title><author>Brugiere, N ; Dubois, F ; Limami, A.M ; Lelandais, M ; Roux, Y ; Sangwan, R.S ; Hirel, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-bab87f285256e73e18dfdaee92104f20b27d5b8028e03b18d1d72ead04ba4f333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Amino acids</topic><topic>ammonium compounds</topic><topic>antisense DNA</topic><topic>chemical constituents of plants</topic><topic>complementary DNA</topic><topic>enzyme activity</topic><topic>free amino acids</topic><topic>gene expression</topic><topic>glutamate-ammonia ligase</topic><topic>immunocytochemistry</topic><topic>Leaves</topic><topic>messenger RNA</topic><topic>Nicotiana plumbaginifolia</topic><topic>Nicotiana tabacum</topic><topic>Nitrogen</topic><topic>nitrogen metabolism</topic><topic>Phloem</topic><topic>Phloem companion cells</topic><topic>Plant cells</topic><topic>Plant roots</topic><topic>Plants</topic><topic>proline</topic><topic>promoter regions</topic><topic>recombinant DNA</topic><topic>roots</topic><topic>salinity</topic><topic>sodium chloride</topic><topic>Stems</topic><topic>stress</topic><topic>superoxide dismutase</topic><topic>Transgenic plants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brugiere, N</creatorcontrib><creatorcontrib>Dubois, F</creatorcontrib><creatorcontrib>Limami, A.M</creatorcontrib><creatorcontrib>Lelandais, M</creatorcontrib><creatorcontrib>Roux, Y</creatorcontrib><creatorcontrib>Sangwan, R.S</creatorcontrib><creatorcontrib>Hirel, B</creatorcontrib><collection>AGRIS</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</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>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>The Plant cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brugiere, N</au><au>Dubois, F</au><au>Limami, A.M</au><au>Lelandais, M</au><au>Roux, Y</au><au>Sangwan, R.S</au><au>Hirel, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glutamine synthetase in the phloem plays a major role in controlling proline production</atitle><jtitle>The Plant cell</jtitle><addtitle>Plant Cell</addtitle><date>1999-10-01</date><risdate>1999</risdate><volume>11</volume><issue>10</issue><spage>1995</spage><epage>2011</epage><pages>1995-2011</pages><issn>1040-4651</issn><eissn>1532-298X</eissn><abstract>To inhibit expression specifically in the phloem, a 274-bp fragment of a cDNA (Gln1-5) encoding cytosolic glutamine synthetase (GS1) from tobacco was placed in the antisense orientation downstream of the cytosolic Cu/Zn superoxide dismutase promoter of Nicotiana plumbaginifolia. After Agrobacterium-mediated transformation, two transgenic N. tabacum lines exhibiting reduced levels of GS1 mRNA and GS activity in midribs, stems, and roots were obtained. Immunogold labeling experiments allowed us to verify that the GS protein content was markedly decreased in the phloem companion cells of transformed plants. Moreover, a general decrease in proline content in the transgenic plants in comparison with wild-type tobacco was observed when plants were forced to assimilate large amounts of ammonium. In contrast, no major changes in the concentration of amino acids used for nitrogen transport were apparent. A 15NH4(+)-labeling kinetic over a 48-hr period confirmed that in leaves of transgenic plants, the decrease in proline production was directly related to glutamine availability. After 2 weeks of salt treatment, the transgenic plants had a pronounced stress phenotype, consisting of wilting and bleaching in the older leaves. We conclude that GS in the phloem plays a major role in regulating proline production consistent with the function of proline as a nitrogen source and as a key metabolite synthesized in response to water stress.</abstract><cop>United States</cop><pub>American Society of Plant Physiologists</pub><pmid>10521528</pmid><doi>10.1105/tpc.11.10.1995</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1040-4651
ispartof The Plant cell, 1999-10, Vol.11 (10), p.1995-2011
issn 1040-4651
1532-298X
language eng
recordid cdi_proquest_miscellaneous_1859309388
source Oxford Journals Online; JSTOR Archival Journals
subjects Amino acids
ammonium compounds
antisense DNA
chemical constituents of plants
complementary DNA
enzyme activity
free amino acids
gene expression
glutamate-ammonia ligase
immunocytochemistry
Leaves
messenger RNA
Nicotiana plumbaginifolia
Nicotiana tabacum
Nitrogen
nitrogen metabolism
Phloem
Phloem companion cells
Plant cells
Plant roots
Plants
proline
promoter regions
recombinant DNA
roots
salinity
sodium chloride
Stems
stress
superoxide dismutase
Transgenic plants
title Glutamine synthetase in the phloem plays a major role in controlling proline production
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-15T09%3A09%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Glutamine%20synthetase%20in%20the%20phloem%20plays%20a%20major%20role%20in%20controlling%20proline%20production&rft.jtitle=The%20Plant%20cell&rft.au=Brugiere,%20N&rft.date=1999-10-01&rft.volume=11&rft.issue=10&rft.spage=1995&rft.epage=2011&rft.pages=1995-2011&rft.issn=1040-4651&rft.eissn=1532-298X&rft_id=info:doi/10.1105/tpc.11.10.1995&rft_dat=%3Cjstor_proqu%3E3871093%3C/jstor_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c447t-bab87f285256e73e18dfdaee92104f20b27d5b8028e03b18d1d72ead04ba4f333%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=218778637&rft_id=info:pmid/10521528&rft_jstor_id=3871093&rfr_iscdi=true