Subcellular and tissue localization of NAD kinases from Arabidopsis: compartmentalization of de novo NADP biosynthesis
The de novo biosynthesis of the triphosphopyridine NADP is catalyzed solely by the ubiquitous NAD kinase family. The Arabidopsis (Arabidopsis thaliana) genome contains two genes encoding NAD⁺ kinases (NADKs), annotated as NADK1, NADK2, and one gene encoding a NADH kinase, NADK3, the latter isoform p...
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description | The de novo biosynthesis of the triphosphopyridine NADP is catalyzed solely by the ubiquitous NAD kinase family. The Arabidopsis (Arabidopsis thaliana) genome contains two genes encoding NAD⁺ kinases (NADKs), annotated as NADK1, NADK2, and one gene encoding a NADH kinase, NADK3, the latter isoform preferring NADH as a substrate. Here, we examined the tissue-specific and developmental expression patterns of the three NADKs using transgenic plants stably transformed with NADK promoter::glucuronidase (GUS) reporter gene constructs. We observed distinct spatial and temporal patterns of GUS activity among the NADK::GUS plants. All three NADK::GUS transgenes were expressed in reproductive tissue, whereas NADK1::GUS activity was found mainly in the roots, NADK2::GUS in leaves, and NADK3::GUS was restricted primarily to leaf vasculature and lateral root primordia. We also examined the subcellular distribution of the three NADK isoforms using NADK-green fluorescent protein (GFP) fusion proteins expressed transiently in Arabidopsis suspension-cultured cells. NADK1 and NADK2 were found to be localized to the cytosol and plastid stroma, respectively, consistent with previous work, whereas NADK3 localized to the peroxisomal matrix via a novel type 1 peroxisomal targeting signal. The specific subcellular and tissue distribution profiles among the three NADK isoforms and their possible non-overlapping roles in NADP(H) biosynthesis in plant cells are discussed. |
doi_str_mv | 10.1007/s00425-009-1047-7 |
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The Arabidopsis (Arabidopsis thaliana) genome contains two genes encoding NAD⁺ kinases (NADKs), annotated as NADK1, NADK2, and one gene encoding a NADH kinase, NADK3, the latter isoform preferring NADH as a substrate. Here, we examined the tissue-specific and developmental expression patterns of the three NADKs using transgenic plants stably transformed with NADK promoter::glucuronidase (GUS) reporter gene constructs. We observed distinct spatial and temporal patterns of GUS activity among the NADK::GUS plants. All three NADK::GUS transgenes were expressed in reproductive tissue, whereas NADK1::GUS activity was found mainly in the roots, NADK2::GUS in leaves, and NADK3::GUS was restricted primarily to leaf vasculature and lateral root primordia. We also examined the subcellular distribution of the three NADK isoforms using NADK-green fluorescent protein (GFP) fusion proteins expressed transiently in Arabidopsis suspension-cultured cells. NADK1 and NADK2 were found to be localized to the cytosol and plastid stroma, respectively, consistent with previous work, whereas NADK3 localized to the peroxisomal matrix via a novel type 1 peroxisomal targeting signal. The specific subcellular and tissue distribution profiles among the three NADK isoforms and their possible non-overlapping roles in NADP(H) biosynthesis in plant cells are discussed.</description><identifier>ISSN: 0032-0935</identifier><identifier>EISSN: 1432-2048</identifier><identifier>DOI: 10.1007/s00425-009-1047-7</identifier><identifier>PMID: 19921251</identifier><identifier>CODEN: PLANAB</identifier><language>eng</language><publisher>Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag</publisher><subject>Agriculture ; Amino Acid Motifs ; Arabidopsis - cytology ; Arabidopsis - enzymology ; Arabidopsis - growth & development ; Biological and medical sciences ; Biomedical and Life Sciences ; Biosynthesis ; Cell Compartmentation ; Cell Membrane Permeability ; Cell membranes ; Cytosol ; Ecology ; Enzymes ; Flowers - cytology ; Flowers - enzymology ; Forestry ; Fundamental and applied biological sciences. Psychology ; Germination - physiology ; Green Fluorescent Proteins - metabolism ; Leaves ; Life Sciences ; NADP - biosynthesis ; Organ Specificity ; Original Article ; Oxidative stress ; Peroxisomes ; Phosphotransferases (Alcohol Group Acceptor) - chemistry ; Phosphotransferases (Alcohol Group Acceptor) - metabolism ; Plant cells ; Plant Leaves - cytology ; Plant Leaves - enzymology ; Plant Leaves - growth & development ; Plant Sciences ; Plants ; Protein isoforms ; Protein Transport ; Proteins ; Recombinant Fusion Proteins - metabolism ; Subcellular Fractions - enzymology ; Transgenic plants</subject><ispartof>Planta, 2010-01, Vol.231 (2), p.305-317</ispartof><rights>Springer-Verlag Berlin Heidelberg 2010</rights><rights>Springer-Verlag 2009</rights><rights>2015 INIST-CNRS</rights><rights>Springer-Verlag 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-19d2c776287690286bf31425558a6dcdbc1e67bddb54202d447b4c9bcaa1afb93</citedby><cites>FETCH-LOGICAL-c512t-19d2c776287690286bf31425558a6dcdbc1e67bddb54202d447b4c9bcaa1afb93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/23391027$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/23391027$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27924,27925,41488,42557,51319,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22327250$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19921251$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Waller, Jeffrey C</creatorcontrib><creatorcontrib>Dhanoa, Preetinder K</creatorcontrib><creatorcontrib>Schumann, Uwe</creatorcontrib><creatorcontrib>Mullen, Robert T</creatorcontrib><creatorcontrib>Snedden, Wayne A</creatorcontrib><title>Subcellular and tissue localization of NAD kinases from Arabidopsis: compartmentalization of de novo NADP biosynthesis</title><title>Planta</title><addtitle>Planta</addtitle><addtitle>Planta</addtitle><description>The de novo biosynthesis of the triphosphopyridine NADP is catalyzed solely by the ubiquitous NAD kinase family. The Arabidopsis (Arabidopsis thaliana) genome contains two genes encoding NAD⁺ kinases (NADKs), annotated as NADK1, NADK2, and one gene encoding a NADH kinase, NADK3, the latter isoform preferring NADH as a substrate. Here, we examined the tissue-specific and developmental expression patterns of the three NADKs using transgenic plants stably transformed with NADK promoter::glucuronidase (GUS) reporter gene constructs. We observed distinct spatial and temporal patterns of GUS activity among the NADK::GUS plants. All three NADK::GUS transgenes were expressed in reproductive tissue, whereas NADK1::GUS activity was found mainly in the roots, NADK2::GUS in leaves, and NADK3::GUS was restricted primarily to leaf vasculature and lateral root primordia. We also examined the subcellular distribution of the three NADK isoforms using NADK-green fluorescent protein (GFP) fusion proteins expressed transiently in Arabidopsis suspension-cultured cells. NADK1 and NADK2 were found to be localized to the cytosol and plastid stroma, respectively, consistent with previous work, whereas NADK3 localized to the peroxisomal matrix via a novel type 1 peroxisomal targeting signal. The specific subcellular and tissue distribution profiles among the three NADK isoforms and their possible non-overlapping roles in NADP(H) biosynthesis in plant cells are discussed.</description><subject>Agriculture</subject><subject>Amino Acid Motifs</subject><subject>Arabidopsis - cytology</subject><subject>Arabidopsis - enzymology</subject><subject>Arabidopsis - growth & development</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biosynthesis</subject><subject>Cell Compartmentation</subject><subject>Cell Membrane Permeability</subject><subject>Cell membranes</subject><subject>Cytosol</subject><subject>Ecology</subject><subject>Enzymes</subject><subject>Flowers - cytology</subject><subject>Flowers - enzymology</subject><subject>Forestry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Germination - physiology</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Leaves</subject><subject>Life Sciences</subject><subject>NADP - biosynthesis</subject><subject>Organ Specificity</subject><subject>Original Article</subject><subject>Oxidative stress</subject><subject>Peroxisomes</subject><subject>Phosphotransferases (Alcohol Group Acceptor) - chemistry</subject><subject>Phosphotransferases (Alcohol Group Acceptor) - metabolism</subject><subject>Plant cells</subject><subject>Plant Leaves - cytology</subject><subject>Plant Leaves - enzymology</subject><subject>Plant Leaves - growth & development</subject><subject>Plant Sciences</subject><subject>Plants</subject><subject>Protein isoforms</subject><subject>Protein Transport</subject><subject>Proteins</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Subcellular Fractions - enzymology</subject><subject>Transgenic plants</subject><issn>0032-0935</issn><issn>1432-2048</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kUtv1DAUhS0EoqXwA1gAFhJiFbi2k3jMblSeUgVIpWvLrxQPSTz4JpXKr8dRRoxgwcqW7neO7_Eh5DGDVwxAvkaAmjcVgKoY1LKSd8gpqwWvONSbu-QUoNxBieaEPEDcAZShlPfJCVOKM96wU3JzOVsX-n7uTaZm9HSKiHOgfXKmj7_MFNNIU0c_b9_SH3E0GJB2OQ10m42NPu0x4hvq0rA3eRrCOP2l8oGO6SYt6q_UxoS34_Q9FMlDcq8zPYZHh_OMXL1_9-38Y3Xx5cOn8-1F5RrGp4opz52ULd_IVgHftLYTrERumo1pvfPWsdBK671tag7c17W0tVPWGcNMZ5U4Iy9X331OP-eAkx4iLnnNGNKMWgrRKGBKFvL5P-QuzXksy2kODHhbC1YgtkIuJ8QcOr3PcTD5VjPQSyV6rUSXSvRSiV6Mnx6MZzsEf1QcOijAiwNgsHx6l83oIv7hOBdc8gYKx1cOy2i8Dvm44f9ef7KKdjilfDQVQpVQy_zZOu9M0uY6l4evLktgAUxykIqL37gitqo</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Waller, Jeffrey C</creator><creator>Dhanoa, Preetinder K</creator><creator>Schumann, Uwe</creator><creator>Mullen, Robert T</creator><creator>Snedden, Wayne A</creator><general>Berlin/Heidelberg : Springer-Verlag</general><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>7X2</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>ABUWG</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>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20100101</creationdate><title>Subcellular and tissue localization of NAD kinases from Arabidopsis: compartmentalization of de novo NADP biosynthesis</title><author>Waller, Jeffrey C ; Dhanoa, Preetinder K ; Schumann, Uwe ; Mullen, Robert T ; Snedden, Wayne A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-19d2c776287690286bf31425558a6dcdbc1e67bddb54202d447b4c9bcaa1afb93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Agriculture</topic><topic>Amino Acid Motifs</topic><topic>Arabidopsis - cytology</topic><topic>Arabidopsis - enzymology</topic><topic>Arabidopsis - growth & development</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biosynthesis</topic><topic>Cell Compartmentation</topic><topic>Cell Membrane Permeability</topic><topic>Cell membranes</topic><topic>Cytosol</topic><topic>Ecology</topic><topic>Enzymes</topic><topic>Flowers - cytology</topic><topic>Flowers - enzymology</topic><topic>Forestry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Germination - physiology</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Leaves</topic><topic>Life Sciences</topic><topic>NADP - biosynthesis</topic><topic>Organ Specificity</topic><topic>Original Article</topic><topic>Oxidative stress</topic><topic>Peroxisomes</topic><topic>Phosphotransferases (Alcohol Group Acceptor) - chemistry</topic><topic>Phosphotransferases (Alcohol Group Acceptor) - metabolism</topic><topic>Plant cells</topic><topic>Plant Leaves - cytology</topic><topic>Plant Leaves - enzymology</topic><topic>Plant Leaves - growth & development</topic><topic>Plant Sciences</topic><topic>Plants</topic><topic>Protein isoforms</topic><topic>Protein Transport</topic><topic>Proteins</topic><topic>Recombinant Fusion Proteins - metabolism</topic><topic>Subcellular Fractions - enzymology</topic><topic>Transgenic plants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Waller, Jeffrey C</creatorcontrib><creatorcontrib>Dhanoa, Preetinder K</creatorcontrib><creatorcontrib>Schumann, Uwe</creatorcontrib><creatorcontrib>Mullen, Robert T</creatorcontrib><creatorcontrib>Snedden, Wayne A</creatorcontrib><collection>AGRIS</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>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Agricultural Science Collection</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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Planta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Waller, Jeffrey C</au><au>Dhanoa, Preetinder K</au><au>Schumann, Uwe</au><au>Mullen, Robert T</au><au>Snedden, Wayne A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subcellular and tissue localization of NAD kinases from Arabidopsis: compartmentalization of de novo NADP biosynthesis</atitle><jtitle>Planta</jtitle><stitle>Planta</stitle><addtitle>Planta</addtitle><date>2010-01-01</date><risdate>2010</risdate><volume>231</volume><issue>2</issue><spage>305</spage><epage>317</epage><pages>305-317</pages><issn>0032-0935</issn><eissn>1432-2048</eissn><coden>PLANAB</coden><abstract>The de novo biosynthesis of the triphosphopyridine NADP is catalyzed solely by the ubiquitous NAD kinase family. The Arabidopsis (Arabidopsis thaliana) genome contains two genes encoding NAD⁺ kinases (NADKs), annotated as NADK1, NADK2, and one gene encoding a NADH kinase, NADK3, the latter isoform preferring NADH as a substrate. Here, we examined the tissue-specific and developmental expression patterns of the three NADKs using transgenic plants stably transformed with NADK promoter::glucuronidase (GUS) reporter gene constructs. We observed distinct spatial and temporal patterns of GUS activity among the NADK::GUS plants. All three NADK::GUS transgenes were expressed in reproductive tissue, whereas NADK1::GUS activity was found mainly in the roots, NADK2::GUS in leaves, and NADK3::GUS was restricted primarily to leaf vasculature and lateral root primordia. We also examined the subcellular distribution of the three NADK isoforms using NADK-green fluorescent protein (GFP) fusion proteins expressed transiently in Arabidopsis suspension-cultured cells. NADK1 and NADK2 were found to be localized to the cytosol and plastid stroma, respectively, consistent with previous work, whereas NADK3 localized to the peroxisomal matrix via a novel type 1 peroxisomal targeting signal. The specific subcellular and tissue distribution profiles among the three NADK isoforms and their possible non-overlapping roles in NADP(H) biosynthesis in plant cells are discussed.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><pmid>19921251</pmid><doi>10.1007/s00425-009-1047-7</doi><tpages>13</tpages></addata></record> |
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subjects | Agriculture Amino Acid Motifs Arabidopsis - cytology Arabidopsis - enzymology Arabidopsis - growth & development Biological and medical sciences Biomedical and Life Sciences Biosynthesis Cell Compartmentation Cell Membrane Permeability Cell membranes Cytosol Ecology Enzymes Flowers - cytology Flowers - enzymology Forestry Fundamental and applied biological sciences. Psychology Germination - physiology Green Fluorescent Proteins - metabolism Leaves Life Sciences NADP - biosynthesis Organ Specificity Original Article Oxidative stress Peroxisomes Phosphotransferases (Alcohol Group Acceptor) - chemistry Phosphotransferases (Alcohol Group Acceptor) - metabolism Plant cells Plant Leaves - cytology Plant Leaves - enzymology Plant Leaves - growth & development Plant Sciences Plants Protein isoforms Protein Transport Proteins Recombinant Fusion Proteins - metabolism Subcellular Fractions - enzymology Transgenic plants |
title | Subcellular and tissue localization of NAD kinases from Arabidopsis: compartmentalization of de novo NADP biosynthesis |
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