P-type ATPase heavy metal transporters with roles in essential zinc homeostasis in Arabidopsis
Arabidopsis thaliana has eight genes encoding members of the type 1B heavy metal-transporting subfamily of the P-type ATPases. Three of these transporters, HMA2, HMA3, and HMA4, are closely related to each other and are most similar in sequence to the divalent heavy metal cation transporters of prok...
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description | Arabidopsis thaliana has eight genes encoding members of the type 1B heavy metal-transporting subfamily of the P-type ATPases. Three of these transporters, HMA2, HMA3, and HMA4, are closely related to each other and are most similar in sequence to the divalent heavy metal cation transporters of prokaryotes. To determine the function of these transporters in metal homeostasis, we have identified and characterized mutants affected in each. Whereas the individual mutants exhibited no apparent phenotype, hma2 hma4 double mutants had a nutritional deficiency phenotype that could be compensated for by increasing the level of Zn, but not Cu or Co, in the growth medium. Levels of Zn, but not other essential elements, in the shoot tissues of a hma2 hma4 double mutant and, to a lesser extent, of a hma4 single mutant were decreased compared with the wild type. Together, these observations indicate a primary role for HMA2 and HMA4 in essential Zn homeostasis. HMA2promoter- and HMA4promoter-reporter gene constructs provide evidence that HMA2 and HMA4 expression is predominantly in the vascular tissues of roots, stems, and leaves. In addition, expression of the genes in developing anthers was confirmed by RT-PCR and was consistent with a male-sterile phenotype in the double mutant. HMA2 appears to be localized to the plasma membrane, as indicated by protein gel blot analysis of membrane fractions using isoform-specific antibodies and by the visualization of an HMA2-green fluorescent protein fusion by confocal microscopy. These observations are consistent with a role for HMA2 and HMA4 in Zn translocation. hma2 and hma4 mutations both conferred increased sensitivity to Cd in a phytochelatin-deficient mutant background, suggesting that they may also influence Cd detoxification. |
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Three of these transporters, HMA2, HMA3, and HMA4, are closely related to each other and are most similar in sequence to the divalent heavy metal cation transporters of prokaryotes. To determine the function of these transporters in metal homeostasis, we have identified and characterized mutants affected in each. Whereas the individual mutants exhibited no apparent phenotype, hma2 hma4 double mutants had a nutritional deficiency phenotype that could be compensated for by increasing the level of Zn, but not Cu or Co, in the growth medium. Levels of Zn, but not other essential elements, in the shoot tissues of a hma2 hma4 double mutant and, to a lesser extent, of a hma4 single mutant were decreased compared with the wild type. Together, these observations indicate a primary role for HMA2 and HMA4 in essential Zn homeostasis. HMA2promoter- and HMA4promoter-reporter gene constructs provide evidence that HMA2 and HMA4 expression is predominantly in the vascular tissues of roots, stems, and leaves. In addition, expression of the genes in developing anthers was confirmed by RT-PCR and was consistent with a male-sterile phenotype in the double mutant. HMA2 appears to be localized to the plasma membrane, as indicated by protein gel blot analysis of membrane fractions using isoform-specific antibodies and by the visualization of an HMA2-green fluorescent protein fusion by confocal microscopy. These observations are consistent with a role for HMA2 and HMA4 in Zn translocation. hma2 and hma4 mutations both conferred increased sensitivity to Cd in a phytochelatin-deficient mutant background, suggesting that they may also influence Cd detoxification.</description><identifier>ISSN: 1040-4651</identifier><identifier>EISSN: 1532-298X</identifier><identifier>DOI: 10.1105/tpc.020487</identifier><identifier>PMID: 15100400</identifier><language>eng</language><publisher>England: American Society of Plant Biologists</publisher><subject>Adenosine triphosphatases ; Adenosine Triphosphatases - genetics ; Adenosine Triphosphatases - metabolism ; Alleles ; Amino Acid Sequence ; Anthers ; Arabidopsis - enzymology ; Arabidopsis - genetics ; Arabidopsis - metabolism ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - metabolism ; Arabidopsis thaliana ; Base Sequence ; bioaccumulation ; Cadmium ; Cation Transport Proteins - genetics ; Cation Transport Proteins - metabolism ; Cell membranes ; Detoxification ; Flowers - genetics ; gene expression ; Genotype ; Green Fluorescent Proteins ; Heavy metals ; Homeostasis ; ion transport ; ion transporting ATPases ; leaves ; Luminescent Proteins - genetics ; messenger RNA ; metal tolerance ; Molecular Sequence Data ; mutants ; Phenotype ; Phenotypes ; Plant cells ; Plant roots ; Plant tissues ; Plants ; Plants, Genetically Modified ; plasma membrane ; Proteins ; Recombinant Fusion Proteins - metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - genetics ; roots ; shoots ; stems ; Translocation ; Zinc ; Zinc - metabolism</subject><ispartof>The Plant cell, 2004-05, Vol.16 (5), p.1327-1339</ispartof><rights>Copyright 2004 American Society of Plant Biologists</rights><rights>Copyright American Society of Plant Physiologists May 2004</rights><rights>Copyright © 2004, American Society of Plant Biologists 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c550t-f0a3b69c8785b774de9f11f1a8cfba1c8bf85aaefdfc4af01cf4ad98e45151943</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3872091$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3872091$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,881,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15100400$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hussain, D</creatorcontrib><creatorcontrib>Haydon, M.J</creatorcontrib><creatorcontrib>Wang, Y</creatorcontrib><creatorcontrib>Wong, E</creatorcontrib><creatorcontrib>Sherson, S.M</creatorcontrib><creatorcontrib>Young, J</creatorcontrib><creatorcontrib>Camakaris, J</creatorcontrib><creatorcontrib>Harper, J.F</creatorcontrib><creatorcontrib>Cobbett, C.S</creatorcontrib><title>P-type ATPase heavy metal transporters with roles in essential zinc homeostasis in Arabidopsis</title><title>The Plant cell</title><addtitle>Plant Cell</addtitle><description>Arabidopsis thaliana has eight genes encoding members of the type 1B heavy metal-transporting subfamily of the P-type ATPases. Three of these transporters, HMA2, HMA3, and HMA4, are closely related to each other and are most similar in sequence to the divalent heavy metal cation transporters of prokaryotes. To determine the function of these transporters in metal homeostasis, we have identified and characterized mutants affected in each. Whereas the individual mutants exhibited no apparent phenotype, hma2 hma4 double mutants had a nutritional deficiency phenotype that could be compensated for by increasing the level of Zn, but not Cu or Co, in the growth medium. Levels of Zn, but not other essential elements, in the shoot tissues of a hma2 hma4 double mutant and, to a lesser extent, of a hma4 single mutant were decreased compared with the wild type. Together, these observations indicate a primary role for HMA2 and HMA4 in essential Zn homeostasis. HMA2promoter- and HMA4promoter-reporter gene constructs provide evidence that HMA2 and HMA4 expression is predominantly in the vascular tissues of roots, stems, and leaves. In addition, expression of the genes in developing anthers was confirmed by RT-PCR and was consistent with a male-sterile phenotype in the double mutant. HMA2 appears to be localized to the plasma membrane, as indicated by protein gel blot analysis of membrane fractions using isoform-specific antibodies and by the visualization of an HMA2-green fluorescent protein fusion by confocal microscopy. These observations are consistent with a role for HMA2 and HMA4 in Zn translocation. hma2 and hma4 mutations both conferred increased sensitivity to Cd in a phytochelatin-deficient mutant background, suggesting that they may also influence Cd detoxification.</description><subject>Adenosine triphosphatases</subject><subject>Adenosine Triphosphatases - genetics</subject><subject>Adenosine Triphosphatases - metabolism</subject><subject>Alleles</subject><subject>Amino Acid Sequence</subject><subject>Anthers</subject><subject>Arabidopsis - enzymology</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Arabidopsis thaliana</subject><subject>Base Sequence</subject><subject>bioaccumulation</subject><subject>Cadmium</subject><subject>Cation Transport Proteins - genetics</subject><subject>Cation Transport Proteins - metabolism</subject><subject>Cell membranes</subject><subject>Detoxification</subject><subject>Flowers - genetics</subject><subject>gene expression</subject><subject>Genotype</subject><subject>Green Fluorescent Proteins</subject><subject>Heavy metals</subject><subject>Homeostasis</subject><subject>ion transport</subject><subject>ion transporting ATPases</subject><subject>leaves</subject><subject>Luminescent Proteins - genetics</subject><subject>messenger RNA</subject><subject>metal tolerance</subject><subject>Molecular Sequence Data</subject><subject>mutants</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Plant cells</subject><subject>Plant roots</subject><subject>Plant tissues</subject><subject>Plants</subject><subject>Plants, Genetically Modified</subject><subject>plasma membrane</subject><subject>Proteins</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - genetics</subject><subject>roots</subject><subject>shoots</subject><subject>stems</subject><subject>Translocation</subject><subject>Zinc</subject><subject>Zinc - 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metabolism</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - genetics</topic><topic>roots</topic><topic>shoots</topic><topic>stems</topic><topic>Translocation</topic><topic>Zinc</topic><topic>Zinc - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hussain, D</creatorcontrib><creatorcontrib>Haydon, M.J</creatorcontrib><creatorcontrib>Wang, Y</creatorcontrib><creatorcontrib>Wong, E</creatorcontrib><creatorcontrib>Sherson, S.M</creatorcontrib><creatorcontrib>Young, J</creatorcontrib><creatorcontrib>Camakaris, J</creatorcontrib><creatorcontrib>Harper, J.F</creatorcontrib><creatorcontrib>Cobbett, C.S</creatorcontrib><collection>AGRIS</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>Docstoc</collection><collection>Biotechnology Research 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>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 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>Science 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>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Plant cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hussain, D</au><au>Haydon, M.J</au><au>Wang, Y</au><au>Wong, E</au><au>Sherson, S.M</au><au>Young, J</au><au>Camakaris, J</au><au>Harper, J.F</au><au>Cobbett, C.S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>P-type ATPase heavy metal transporters with roles in essential zinc homeostasis in Arabidopsis</atitle><jtitle>The Plant cell</jtitle><addtitle>Plant Cell</addtitle><date>2004-05-01</date><risdate>2004</risdate><volume>16</volume><issue>5</issue><spage>1327</spage><epage>1339</epage><pages>1327-1339</pages><issn>1040-4651</issn><eissn>1532-298X</eissn><abstract>Arabidopsis thaliana has eight genes encoding members of the type 1B heavy metal-transporting subfamily of the P-type ATPases. Three of these transporters, HMA2, HMA3, and HMA4, are closely related to each other and are most similar in sequence to the divalent heavy metal cation transporters of prokaryotes. To determine the function of these transporters in metal homeostasis, we have identified and characterized mutants affected in each. Whereas the individual mutants exhibited no apparent phenotype, hma2 hma4 double mutants had a nutritional deficiency phenotype that could be compensated for by increasing the level of Zn, but not Cu or Co, in the growth medium. Levels of Zn, but not other essential elements, in the shoot tissues of a hma2 hma4 double mutant and, to a lesser extent, of a hma4 single mutant were decreased compared with the wild type. Together, these observations indicate a primary role for HMA2 and HMA4 in essential Zn homeostasis. HMA2promoter- and HMA4promoter-reporter gene constructs provide evidence that HMA2 and HMA4 expression is predominantly in the vascular tissues of roots, stems, and leaves. In addition, expression of the genes in developing anthers was confirmed by RT-PCR and was consistent with a male-sterile phenotype in the double mutant. HMA2 appears to be localized to the plasma membrane, as indicated by protein gel blot analysis of membrane fractions using isoform-specific antibodies and by the visualization of an HMA2-green fluorescent protein fusion by confocal microscopy. These observations are consistent with a role for HMA2 and HMA4 in Zn translocation. hma2 and hma4 mutations both conferred increased sensitivity to Cd in a phytochelatin-deficient mutant background, suggesting that they may also influence Cd detoxification.</abstract><cop>England</cop><pub>American Society of Plant Biologists</pub><pmid>15100400</pmid><doi>10.1105/tpc.020487</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine triphosphatases Adenosine Triphosphatases - genetics Adenosine Triphosphatases - metabolism Alleles Amino Acid Sequence Anthers Arabidopsis - enzymology Arabidopsis - genetics Arabidopsis - metabolism Arabidopsis Proteins - genetics Arabidopsis Proteins - metabolism Arabidopsis thaliana Base Sequence bioaccumulation Cadmium Cation Transport Proteins - genetics Cation Transport Proteins - metabolism Cell membranes Detoxification Flowers - genetics gene expression Genotype Green Fluorescent Proteins Heavy metals Homeostasis ion transport ion transporting ATPases leaves Luminescent Proteins - genetics messenger RNA metal tolerance Molecular Sequence Data mutants Phenotype Phenotypes Plant cells Plant roots Plant tissues Plants Plants, Genetically Modified plasma membrane Proteins Recombinant Fusion Proteins - metabolism Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - genetics roots shoots stems Translocation Zinc Zinc - metabolism |
title | P-type ATPase heavy metal transporters with roles in essential zinc homeostasis in Arabidopsis |
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