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...
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Veröffentlicht in: | Plant molecular biology 1999-03, Vol.39 (4), p.847-857 |
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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 |
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(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. 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(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 & 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 & 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>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> |
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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 |
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