Cloning sulfur assimilation genes of Brassica juncea L.: cadmium differentially affects the expression of a putative low-affinity sulfate transporter and isoforms of ATP sulfurylase and APS reductase

The heavy-metal accumulator Brassica juncea L. is a high-biomass crop able to extract heavy-metal ions from the soil, a substantial part being translocated from root to shoot. Previous work has shown that Cd accumulation is accompanied by massive formation of phytochelatins (PCs). Rapid de novo synt...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Plant molecular biology 1999-03, Vol.39 (4), p.847-857
Hauptverfasser: Heiss, S. (Ruprecht-Karls-Universitaet, Heidelberg (Germany). Botanisches Inst.), Schafer, H.J, Haag-Kerwer, A, Rausch, T
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 857
container_issue 4
container_start_page 847
container_title Plant molecular biology
container_volume 39
creator Heiss, S. (Ruprecht-Karls-Universitaet, Heidelberg (Germany). Botanisches Inst.)
Schafer, H.J
Haag-Kerwer, A
Rausch, T
description The heavy-metal accumulator Brassica juncea L. is a high-biomass crop able to extract heavy-metal ions from the soil, a substantial part being translocated from root to shoot. Previous work has shown that Cd accumulation is accompanied by massive formation of phytochelatins (PCs). Rapid de novo synthesis of PCs in roots and leaves requires an increased synthesis of the tripeptide glutathione (GSH), which in turn depends on increased sulfur assimilation. Therefore. we have cloned cDNAs for three enzymes involved in sulfur assimilation, i.e. a putative low-affinity sulfate transporter (LAST) and two isoforms each for ATP sulfurylase (ATPS) and APS reductase (APSR). As degradation of glucosinolates might provide an additional sulfur source under stress, we also cloned a myrosinase (MYR). RNA blot analysis of transcript amounts indicated that upon Cd exposure (25 microM) the expression of ATPS and APSR in roots and leaves of 6-week-old Brassica juncea plants was strongly increased, whereas the expression of MYR was unaffected. LAST transcripts were significantly reduced in the root but remained unchanged in the leaves. Concomitant with Cd induction of ATPS and APSR mRNAs, cysteine concentrations in roots and leaves increased by 81% and 25%, respectively, whereas GSH concentrations decreased in roots and leaves by 39% and 48%, respectively. In agreement with our previous report on Cd induction of gamma-glutamylcysteine synthetase in B. juncea, the results indicate coordinate changes of expression for several sulfur assimilation enzymes in response to an increased demand for cysteine during PC synthesis.
doi_str_mv 10.1023/A:1006169717355
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_69788805</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>69788805</sourcerecordid><originalsourceid>FETCH-LOGICAL-c333t-555b62abe924a81205085f071096475073145ba4ad7f3ad4adeffcf6eee45e003</originalsourceid><addsrcrecordid>eNqFkU2P0zAQhi0EYsvCmRPI4sAtix3HcbK3UvElVbASyzmaJuPiyrGDP4D-Qv4WplsuXDiNPH78-rGHkKecXXFWi1fra85Yy9tecSWkvEdWXCpRSVZ398mK8VZVTcPrC_IoxgNjBRbtQ3LBmZCM9WpFfm2sd8btacxW50AhRjMbC8l4R_foMFKv6evwpz8CPWQ3ItDt1TUdYZpNnulktMaALhmw9kihrMYUafqKFH8uAcvBElVCgC45leDvSK3_URXQOJOOp5shIU0BXFx8SFg03ERN9NqH-SSwvr05Gx4tRDztr28-04BTHlPpPCYPNNiIT871knx5--Z2877afnr3YbPeVqMQIlVSyl1bww77uoGO10yyTmqmOOvbRkmmBG_kDhqYlBYwlYpaj7pFxEZi-b1L8vIudwn-W8aYhtnEEa0Fhz7HoUyi6zom_wtyVddStl0BX_wDHnwOrjxiUKrYCNHWBXp-hvJuxmlYgpkhHIe_gyzAsztAgx9gH0wcPm553_fFuS8ZvwHqGqwY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>771453362</pqid></control><display><type>article</type><title>Cloning sulfur assimilation genes of Brassica juncea L.: cadmium differentially affects the expression of a putative low-affinity sulfate transporter and isoforms of ATP sulfurylase and APS reductase</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Heiss, S. (Ruprecht-Karls-Universitaet, Heidelberg (Germany). Botanisches Inst.) ; Schafer, H.J ; Haag-Kerwer, A ; Rausch, T</creator><creatorcontrib>Heiss, S. (Ruprecht-Karls-Universitaet, Heidelberg (Germany). Botanisches Inst.) ; Schafer, H.J ; Haag-Kerwer, A ; Rausch, T</creatorcontrib><description>The heavy-metal accumulator Brassica juncea L. is a high-biomass crop able to extract heavy-metal ions from the soil, a substantial part being translocated from root to shoot. Previous work has shown that Cd accumulation is accompanied by massive formation of phytochelatins (PCs). Rapid de novo synthesis of PCs in roots and leaves requires an increased synthesis of the tripeptide glutathione (GSH), which in turn depends on increased sulfur assimilation. Therefore. we have cloned cDNAs for three enzymes involved in sulfur assimilation, i.e. a putative low-affinity sulfate transporter (LAST) and two isoforms each for ATP sulfurylase (ATPS) and APS reductase (APSR). As degradation of glucosinolates might provide an additional sulfur source under stress, we also cloned a myrosinase (MYR). RNA blot analysis of transcript amounts indicated that upon Cd exposure (25 microM) the expression of ATPS and APSR in roots and leaves of 6-week-old Brassica juncea plants was strongly increased, whereas the expression of MYR was unaffected. LAST transcripts were significantly reduced in the root but remained unchanged in the leaves. Concomitant with Cd induction of ATPS and APSR mRNAs, cysteine concentrations in roots and leaves increased by 81% and 25%, respectively, whereas GSH concentrations decreased in roots and leaves by 39% and 48%, respectively. In agreement with our previous report on Cd induction of gamma-glutamylcysteine synthetase in B. juncea, the results indicate coordinate changes of expression for several sulfur assimilation enzymes in response to an increased demand for cysteine during PC synthesis.</description><identifier>ISSN: 0167-4412</identifier><identifier>EISSN: 1573-5028</identifier><identifier>DOI: 10.1023/A:1006169717355</identifier><identifier>PMID: 10350097</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Amino Acid Sequence ; Amino acids ; ANABOLISM ; ANABOLISME ; ANABOLISMO ; ATP ; AZUFRE ; Biological Evolution ; Biological Transport ; Brassica - genetics ; Brassica - metabolism ; BRASSICA JUNCEA ; CADMIO ; CADMIUM ; Cadmium Compounds - pharmacokinetics ; Cadmium Compounds - pharmacology ; Carrier Proteins - chemistry ; Carrier Proteins - genetics ; Carrier Proteins - metabolism ; CLONACION MOLECULAR ; CLONAGE MOLECULAIRE ; Cloning ; Cloning, Molecular ; Crops ; Energy crops ; Enzyme Induction ; Enzymes ; GENE ; Gene expression ; Gene Expression Regulation, Enzymologic - drug effects ; Gene Expression Regulation, Plant - drug effects ; GENES ; Genomics ; Heavy metals ; Isoenzymes - genetics ; Kinetics ; Leaves ; Membrane Transport Proteins ; MIROSINASA ; MOLECULAR CLONING ; Molecular Sequence Data ; MYROSINASE ; Nitrates - pharmacokinetics ; Nitrates - pharmacology ; OXIDOREDUCTASES ; Oxidoreductases - chemistry ; Oxidoreductases - genetics ; Oxidoreductases - metabolism ; Oxidoreductases Acting on Sulfur Group Donors ; OXIDORREDUCTASAS ; OXYDOREDUCTASE ; Recombinant Proteins - biosynthesis ; Recombinant Proteins - chemistry ; Recombinant Proteins - metabolism ; Roots ; Sequence Alignment ; Sequence Homology, Amino Acid ; SOUFRE ; Space life sciences ; Sulfate Adenylyltransferase - chemistry ; Sulfate Adenylyltransferase - genetics ; Sulfate Adenylyltransferase - metabolism ; Sulfate Transporters ; Sulfates ; Sulfates - metabolism ; Sulfur ; SULPHUR ; Transcription, Genetic - drug effects</subject><ispartof>Plant molecular biology, 1999-03, Vol.39 (4), p.847-857</ispartof><rights>Kluwer Academic Publishers 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c333t-555b62abe924a81205085f071096475073145ba4ad7f3ad4adeffcf6eee45e003</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10350097$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heiss, S. (Ruprecht-Karls-Universitaet, Heidelberg (Germany). Botanisches Inst.)</creatorcontrib><creatorcontrib>Schafer, H.J</creatorcontrib><creatorcontrib>Haag-Kerwer, A</creatorcontrib><creatorcontrib>Rausch, T</creatorcontrib><title>Cloning sulfur assimilation genes of Brassica juncea L.: cadmium differentially affects the expression of a putative low-affinity sulfate transporter and isoforms of ATP sulfurylase and APS reductase</title><title>Plant molecular biology</title><addtitle>Plant Mol Biol</addtitle><description>The heavy-metal accumulator Brassica juncea L. is a high-biomass crop able to extract heavy-metal ions from the soil, a substantial part being translocated from root to shoot. Previous work has shown that Cd accumulation is accompanied by massive formation of phytochelatins (PCs). Rapid de novo synthesis of PCs in roots and leaves requires an increased synthesis of the tripeptide glutathione (GSH), which in turn depends on increased sulfur assimilation. Therefore. we have cloned cDNAs for three enzymes involved in sulfur assimilation, i.e. a putative low-affinity sulfate transporter (LAST) and two isoforms each for ATP sulfurylase (ATPS) and APS reductase (APSR). As degradation of glucosinolates might provide an additional sulfur source under stress, we also cloned a myrosinase (MYR). RNA blot analysis of transcript amounts indicated that upon Cd exposure (25 microM) the expression of ATPS and APSR in roots and leaves of 6-week-old Brassica juncea plants was strongly increased, whereas the expression of MYR was unaffected. LAST transcripts were significantly reduced in the root but remained unchanged in the leaves. Concomitant with Cd induction of ATPS and APSR mRNAs, cysteine concentrations in roots and leaves increased by 81% and 25%, respectively, whereas GSH concentrations decreased in roots and leaves by 39% and 48%, respectively. In agreement with our previous report on Cd induction of gamma-glutamylcysteine synthetase in B. juncea, the results indicate coordinate changes of expression for several sulfur assimilation enzymes in response to an increased demand for cysteine during PC synthesis.</description><subject>Amino Acid Sequence</subject><subject>Amino acids</subject><subject>ANABOLISM</subject><subject>ANABOLISME</subject><subject>ANABOLISMO</subject><subject>ATP</subject><subject>AZUFRE</subject><subject>Biological Evolution</subject><subject>Biological Transport</subject><subject>Brassica - genetics</subject><subject>Brassica - metabolism</subject><subject>BRASSICA JUNCEA</subject><subject>CADMIO</subject><subject>CADMIUM</subject><subject>Cadmium Compounds - pharmacokinetics</subject><subject>Cadmium Compounds - pharmacology</subject><subject>Carrier Proteins - chemistry</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - metabolism</subject><subject>CLONACION MOLECULAR</subject><subject>CLONAGE MOLECULAIRE</subject><subject>Cloning</subject><subject>Cloning, Molecular</subject><subject>Crops</subject><subject>Energy crops</subject><subject>Enzyme Induction</subject><subject>Enzymes</subject><subject>GENE</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Enzymologic - drug effects</subject><subject>Gene Expression Regulation, Plant - drug effects</subject><subject>GENES</subject><subject>Genomics</subject><subject>Heavy metals</subject><subject>Isoenzymes - genetics</subject><subject>Kinetics</subject><subject>Leaves</subject><subject>Membrane Transport Proteins</subject><subject>MIROSINASA</subject><subject>MOLECULAR CLONING</subject><subject>Molecular Sequence Data</subject><subject>MYROSINASE</subject><subject>Nitrates - pharmacokinetics</subject><subject>Nitrates - pharmacology</subject><subject>OXIDOREDUCTASES</subject><subject>Oxidoreductases - chemistry</subject><subject>Oxidoreductases - genetics</subject><subject>Oxidoreductases - metabolism</subject><subject>Oxidoreductases Acting on Sulfur Group Donors</subject><subject>OXIDORREDUCTASAS</subject><subject>OXYDOREDUCTASE</subject><subject>Recombinant Proteins - biosynthesis</subject><subject>Recombinant Proteins - chemistry</subject><subject>Recombinant Proteins - metabolism</subject><subject>Roots</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Amino Acid</subject><subject>SOUFRE</subject><subject>Space life sciences</subject><subject>Sulfate Adenylyltransferase - chemistry</subject><subject>Sulfate Adenylyltransferase - genetics</subject><subject>Sulfate Adenylyltransferase - metabolism</subject><subject>Sulfate Transporters</subject><subject>Sulfates</subject><subject>Sulfates - metabolism</subject><subject>Sulfur</subject><subject>SULPHUR</subject><subject>Transcription, Genetic - drug effects</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>eNqFkU2P0zAQhi0EYsvCmRPI4sAtix3HcbK3UvElVbASyzmaJuPiyrGDP4D-Qv4WplsuXDiNPH78-rGHkKecXXFWi1fra85Yy9tecSWkvEdWXCpRSVZ398mK8VZVTcPrC_IoxgNjBRbtQ3LBmZCM9WpFfm2sd8btacxW50AhRjMbC8l4R_foMFKv6evwpz8CPWQ3ItDt1TUdYZpNnulktMaALhmw9kihrMYUafqKFH8uAcvBElVCgC45leDvSK3_URXQOJOOp5shIU0BXFx8SFg03ERN9NqH-SSwvr05Gx4tRDztr28-04BTHlPpPCYPNNiIT871knx5--Z2877afnr3YbPeVqMQIlVSyl1bww77uoGO10yyTmqmOOvbRkmmBG_kDhqYlBYwlYpaj7pFxEZi-b1L8vIudwn-W8aYhtnEEa0Fhz7HoUyi6zom_wtyVddStl0BX_wDHnwOrjxiUKrYCNHWBXp-hvJuxmlYgpkhHIe_gyzAsztAgx9gH0wcPm553_fFuS8ZvwHqGqwY</recordid><startdate>199903</startdate><enddate>199903</enddate><creator>Heiss, S. (Ruprecht-Karls-Universitaet, Heidelberg (Germany). Botanisches Inst.)</creator><creator>Schafer, H.J</creator><creator>Haag-Kerwer, A</creator><creator>Rausch, T</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>199903</creationdate><title>Cloning sulfur assimilation genes of Brassica juncea L.: cadmium differentially affects the expression of a putative low-affinity sulfate transporter and isoforms of ATP sulfurylase and APS reductase</title><author>Heiss, S. (Ruprecht-Karls-Universitaet, Heidelberg (Germany). Botanisches Inst.) ; Schafer, H.J ; Haag-Kerwer, A ; Rausch, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c333t-555b62abe924a81205085f071096475073145ba4ad7f3ad4adeffcf6eee45e003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Amino Acid Sequence</topic><topic>Amino acids</topic><topic>ANABOLISM</topic><topic>ANABOLISME</topic><topic>ANABOLISMO</topic><topic>ATP</topic><topic>AZUFRE</topic><topic>Biological Evolution</topic><topic>Biological Transport</topic><topic>Brassica - genetics</topic><topic>Brassica - metabolism</topic><topic>BRASSICA JUNCEA</topic><topic>CADMIO</topic><topic>CADMIUM</topic><topic>Cadmium Compounds - pharmacokinetics</topic><topic>Cadmium Compounds - pharmacology</topic><topic>Carrier Proteins - chemistry</topic><topic>Carrier Proteins - genetics</topic><topic>Carrier Proteins - metabolism</topic><topic>CLONACION MOLECULAR</topic><topic>CLONAGE MOLECULAIRE</topic><topic>Cloning</topic><topic>Cloning, Molecular</topic><topic>Crops</topic><topic>Energy crops</topic><topic>Enzyme Induction</topic><topic>Enzymes</topic><topic>GENE</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Enzymologic - drug effects</topic><topic>Gene Expression Regulation, Plant - drug effects</topic><topic>GENES</topic><topic>Genomics</topic><topic>Heavy metals</topic><topic>Isoenzymes - genetics</topic><topic>Kinetics</topic><topic>Leaves</topic><topic>Membrane Transport Proteins</topic><topic>MIROSINASA</topic><topic>MOLECULAR CLONING</topic><topic>Molecular Sequence Data</topic><topic>MYROSINASE</topic><topic>Nitrates - pharmacokinetics</topic><topic>Nitrates - pharmacology</topic><topic>OXIDOREDUCTASES</topic><topic>Oxidoreductases - chemistry</topic><topic>Oxidoreductases - genetics</topic><topic>Oxidoreductases - metabolism</topic><topic>Oxidoreductases Acting on Sulfur Group Donors</topic><topic>OXIDORREDUCTASAS</topic><topic>OXYDOREDUCTASE</topic><topic>Recombinant Proteins - biosynthesis</topic><topic>Recombinant Proteins - chemistry</topic><topic>Recombinant Proteins - metabolism</topic><topic>Roots</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Amino Acid</topic><topic>SOUFRE</topic><topic>Space life sciences</topic><topic>Sulfate Adenylyltransferase - chemistry</topic><topic>Sulfate Adenylyltransferase - genetics</topic><topic>Sulfate Adenylyltransferase - metabolism</topic><topic>Sulfate Transporters</topic><topic>Sulfates</topic><topic>Sulfates - metabolism</topic><topic>Sulfur</topic><topic>SULPHUR</topic><topic>Transcription, Genetic - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heiss, S. (Ruprecht-Karls-Universitaet, Heidelberg (Germany). Botanisches Inst.)</creatorcontrib><creatorcontrib>Schafer, H.J</creatorcontrib><creatorcontrib>Haag-Kerwer, A</creatorcontrib><creatorcontrib>Rausch, T</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 &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>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 (ProQuest)</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 &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; 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>Heiss, S. (Ruprecht-Karls-Universitaet, Heidelberg (Germany). Botanisches Inst.)</au><au>Schafer, H.J</au><au>Haag-Kerwer, A</au><au>Rausch, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cloning sulfur assimilation genes of Brassica juncea L.: cadmium differentially affects the expression of a putative low-affinity sulfate transporter and isoforms of ATP sulfurylase and APS reductase</atitle><jtitle>Plant molecular biology</jtitle><addtitle>Plant Mol Biol</addtitle><date>1999-03</date><risdate>1999</risdate><volume>39</volume><issue>4</issue><spage>847</spage><epage>857</epage><pages>847-857</pages><issn>0167-4412</issn><eissn>1573-5028</eissn><abstract>The heavy-metal accumulator Brassica juncea L. is a high-biomass crop able to extract heavy-metal ions from the soil, a substantial part being translocated from root to shoot. Previous work has shown that Cd accumulation is accompanied by massive formation of phytochelatins (PCs). Rapid de novo synthesis of PCs in roots and leaves requires an increased synthesis of the tripeptide glutathione (GSH), which in turn depends on increased sulfur assimilation. Therefore. we have cloned cDNAs for three enzymes involved in sulfur assimilation, i.e. a putative low-affinity sulfate transporter (LAST) and two isoforms each for ATP sulfurylase (ATPS) and APS reductase (APSR). As degradation of glucosinolates might provide an additional sulfur source under stress, we also cloned a myrosinase (MYR). RNA blot analysis of transcript amounts indicated that upon Cd exposure (25 microM) the expression of ATPS and APSR in roots and leaves of 6-week-old Brassica juncea plants was strongly increased, whereas the expression of MYR was unaffected. LAST transcripts were significantly reduced in the root but remained unchanged in the leaves. Concomitant with Cd induction of ATPS and APSR mRNAs, cysteine concentrations in roots and leaves increased by 81% and 25%, respectively, whereas GSH concentrations decreased in roots and leaves by 39% and 48%, respectively. In agreement with our previous report on Cd induction of gamma-glutamylcysteine synthetase in B. juncea, the results indicate coordinate changes of expression for several sulfur assimilation enzymes in response to an increased demand for cysteine during PC synthesis.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>10350097</pmid><doi>10.1023/A:1006169717355</doi><tpages>11</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0167-4412
ispartof Plant molecular biology, 1999-03, Vol.39 (4), p.847-857
issn 0167-4412
1573-5028
language eng
recordid cdi_proquest_miscellaneous_69788805
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Amino Acid Sequence
Amino acids
ANABOLISM
ANABOLISME
ANABOLISMO
ATP
AZUFRE
Biological Evolution
Biological Transport
Brassica - genetics
Brassica - metabolism
BRASSICA JUNCEA
CADMIO
CADMIUM
Cadmium Compounds - pharmacokinetics
Cadmium Compounds - pharmacology
Carrier Proteins - chemistry
Carrier Proteins - genetics
Carrier Proteins - metabolism
CLONACION MOLECULAR
CLONAGE MOLECULAIRE
Cloning
Cloning, Molecular
Crops
Energy crops
Enzyme Induction
Enzymes
GENE
Gene expression
Gene Expression Regulation, Enzymologic - drug effects
Gene Expression Regulation, Plant - drug effects
GENES
Genomics
Heavy metals
Isoenzymes - genetics
Kinetics
Leaves
Membrane Transport Proteins
MIROSINASA
MOLECULAR CLONING
Molecular Sequence Data
MYROSINASE
Nitrates - pharmacokinetics
Nitrates - pharmacology
OXIDOREDUCTASES
Oxidoreductases - chemistry
Oxidoreductases - genetics
Oxidoreductases - metabolism
Oxidoreductases Acting on Sulfur Group Donors
OXIDORREDUCTASAS
OXYDOREDUCTASE
Recombinant Proteins - biosynthesis
Recombinant Proteins - chemistry
Recombinant Proteins - metabolism
Roots
Sequence Alignment
Sequence Homology, Amino Acid
SOUFRE
Space life sciences
Sulfate Adenylyltransferase - chemistry
Sulfate Adenylyltransferase - genetics
Sulfate Adenylyltransferase - metabolism
Sulfate Transporters
Sulfates
Sulfates - metabolism
Sulfur
SULPHUR
Transcription, Genetic - drug effects
title Cloning sulfur assimilation genes of Brassica juncea L.: cadmium differentially affects the expression of a putative low-affinity sulfate transporter and isoforms of ATP sulfurylase and APS reductase
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-14T03%3A42%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cloning%20sulfur%20assimilation%20genes%20of%20Brassica%20juncea%20L.:%20cadmium%20differentially%20affects%20the%20expression%20of%20a%20putative%20low-affinity%20sulfate%20transporter%20and%20isoforms%20of%20ATP%20sulfurylase%20and%20APS%20reductase&rft.jtitle=Plant%20molecular%20biology&rft.au=Heiss,%20S.%20(Ruprecht-Karls-Universitaet,%20Heidelberg%20(Germany).%20Botanisches%20Inst.)&rft.date=1999-03&rft.volume=39&rft.issue=4&rft.spage=847&rft.epage=857&rft.pages=847-857&rft.issn=0167-4412&rft.eissn=1573-5028&rft_id=info:doi/10.1023/A:1006169717355&rft_dat=%3Cproquest_pubme%3E69788805%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=771453362&rft_id=info:pmid/10350097&rfr_iscdi=true