Arabidopsis heavy metal P-type ATPase HMA5 interacts with metallochaperones and functions in copper detoxification of roots

Since copper (Cu) is essential in key physiological oxidation reactions, organisms have developed strategies for handling Cu while avoiding its potentially toxic effects. Among the tools that have evolved to cope with Cu is a network of Cu homeostasis factors such as Cu-transporting P-type ATPases t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Plant journal : for cell and molecular biology 2006, Vol.45 (2), p.225-236
Hauptverfasser: Andrés-Colás, Nuria, Sancenón, Vicente, Rodríguez-Navarro, Susana, Mayo, Sonia, Thiele, Dennis J, Ecker, Joseph R, Puig, Sergi, Peñarrubia, Lola
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 236
container_issue 2
container_start_page 225
container_title The Plant journal : for cell and molecular biology
container_volume 45
creator Andrés-Colás, Nuria
Sancenón, Vicente
Rodríguez-Navarro, Susana
Mayo, Sonia
Thiele, Dennis J
Ecker, Joseph R
Puig, Sergi
Peñarrubia, Lola
description Since copper (Cu) is essential in key physiological oxidation reactions, organisms have developed strategies for handling Cu while avoiding its potentially toxic effects. Among the tools that have evolved to cope with Cu is a network of Cu homeostasis factors such as Cu-transporting P-type ATPases that play a key role in transmembrane Cu transport. In this work we present the functional characterization of an Arabidopsis Cu-transporting P-type ATPase, denoted heavy metal ATPase 5 (HMA5), and its interaction with Arabidopsis metallochaperones. HMA5 is primarily expressed in roots, and is strongly and specifically induced by Cu in whole plants. We have identified and characterized plants carrying two independent T-DNA insertion alleles, hma5-1 and hma5-2. Both mutants are hypersensitive to Cu but not to other metals such as iron, zinc or cadmium. Interestingly, root tips from Cu-treated hma5 mutants exhibit a wave-like phenotype at early stages and later on main root growth completely arrests whereas lateral roots emerge near the crown. Accordingly, these lines accumulate Cu in roots to a greater extent than wild-type plants under Cu excess. Finally, yeast two-hybrid experiments demonstrate that the metal-binding domains of HMA5 interact with Arabidopsis ATX1-like Cu chaperones, and suggest a regulatory role for the plant-specific domain of the CCH Cu chaperone. Based on these findings, we propose a role for HMA5 in Cu compartmentalization and detoxification.
doi_str_mv 10.1111/j.1365-313X.2005.02601.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_20864322</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20864322</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5291-5d617577dc29f17d79e992da9436e16f396a0244409b3382c528d8cc4983acb3</originalsourceid><addsrcrecordid>eNqNkV2L1DAUhoMo7rj6FzQIetearybNhRfDoq6y4oAjeBfOpKmTodPUpHVn8M-b7gwueGVuEnif9-TAgxCmpKT5vNmVlMuq4JR_LxkhVUmYJLQ8PECLv8FDtCBakkIJyi7Qk5R2hFDFpXiMLqjkUmkpF-j3MsLGN2FIPuGtg19HvHcjdHhVjMfB4eV6Bcnh68_LCvt-dBHsmPCtH7cnrgt2C4OLoXcJQ9_gdurt6EOfMo5tGHKGGzeGg2-9hTnBocUxhDE9RY9a6JJ7dr4v0fr9u_XVdXHz5cPHq-VNYSumaVE1kqpKqcYy3VLVKO20Zg1owaWjsuVaAmFCCKI3nNcst-qmtlbomoPd8Ev0-jR2iOHn5NJo9j5Z13XQuzAlw0gtBWcsgy__AXdhin1ezTDKhdaakgzVJ8jGkFJ0rRmi30M8GkrMLMfszOzAzA7MLMfcyTGHXH1-nj9t9q65L55tZODVGYBkoWsj9Nane04JRdQd9_bE3frOHf97AbNefZpfuf_i1G8hGPgR8x_fvrIcEEpqTbjkfwA7K7Pw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>213499910</pqid></control><display><type>article</type><title>Arabidopsis heavy metal P-type ATPase HMA5 interacts with metallochaperones and functions in copper detoxification of roots</title><source>Wiley Free Content</source><source>MEDLINE</source><source>IngentaConnect Free/Open Access Journals</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Andrés-Colás, Nuria ; Sancenón, Vicente ; Rodríguez-Navarro, Susana ; Mayo, Sonia ; Thiele, Dennis J ; Ecker, Joseph R ; Puig, Sergi ; Peñarrubia, Lola</creator><creatorcontrib>Andrés-Colás, Nuria ; Sancenón, Vicente ; Rodríguez-Navarro, Susana ; Mayo, Sonia ; Thiele, Dennis J ; Ecker, Joseph R ; Puig, Sergi ; Peñarrubia, Lola</creatorcontrib><description>Since copper (Cu) is essential in key physiological oxidation reactions, organisms have developed strategies for handling Cu while avoiding its potentially toxic effects. Among the tools that have evolved to cope with Cu is a network of Cu homeostasis factors such as Cu-transporting P-type ATPases that play a key role in transmembrane Cu transport. In this work we present the functional characterization of an Arabidopsis Cu-transporting P-type ATPase, denoted heavy metal ATPase 5 (HMA5), and its interaction with Arabidopsis metallochaperones. HMA5 is primarily expressed in roots, and is strongly and specifically induced by Cu in whole plants. We have identified and characterized plants carrying two independent T-DNA insertion alleles, hma5-1 and hma5-2. Both mutants are hypersensitive to Cu but not to other metals such as iron, zinc or cadmium. Interestingly, root tips from Cu-treated hma5 mutants exhibit a wave-like phenotype at early stages and later on main root growth completely arrests whereas lateral roots emerge near the crown. Accordingly, these lines accumulate Cu in roots to a greater extent than wild-type plants under Cu excess. Finally, yeast two-hybrid experiments demonstrate that the metal-binding domains of HMA5 interact with Arabidopsis ATX1-like Cu chaperones, and suggest a regulatory role for the plant-specific domain of the CCH Cu chaperone. Based on these findings, we propose a role for HMA5 in Cu compartmentalization and detoxification.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/j.1365-313X.2005.02601.x</identifier><identifier>PMID: 16367966</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Science Ltd</publisher><subject>Adenosine Triphosphatases - chemistry ; Adenosine Triphosphatases - genetics ; Adenosine Triphosphatases - metabolism ; Agronomy. Soil science and plant productions ; Amino Acid Sequence ; Arabidopsis ; Arabidopsis - enzymology ; Arabidopsis Proteins - chemistry ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - metabolism ; Base Sequence ; Biological and medical sciences ; Copper - metabolism ; Cu homeostasis ; Cytogenetics ; DNA Primers ; Fundamental and applied biological sciences. Psychology ; Generalities. Genetics. Plant material ; Genes, Plant ; Genetics and breeding of economic plants ; heavy metal P‐type ATPase ; HMA5 ; metal detoxification ; metallochaperones ; Molecular Chaperones - metabolism ; Molecular Sequence Data ; Plant Roots - metabolism ; RNA, Messenger - genetics ; Sequence Homology, Amino Acid</subject><ispartof>The Plant journal : for cell and molecular biology, 2006, Vol.45 (2), p.225-236</ispartof><rights>2006 INIST-CNRS</rights><rights>2005 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5291-5d617577dc29f17d79e992da9436e16f396a0244409b3382c528d8cc4983acb3</citedby><cites>FETCH-LOGICAL-c5291-5d617577dc29f17d79e992da9436e16f396a0244409b3382c528d8cc4983acb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-313X.2005.02601.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-313X.2005.02601.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,4010,27902,27903,27904,45553,45554,46387,46811</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17470766$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16367966$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Andrés-Colás, Nuria</creatorcontrib><creatorcontrib>Sancenón, Vicente</creatorcontrib><creatorcontrib>Rodríguez-Navarro, Susana</creatorcontrib><creatorcontrib>Mayo, Sonia</creatorcontrib><creatorcontrib>Thiele, Dennis J</creatorcontrib><creatorcontrib>Ecker, Joseph R</creatorcontrib><creatorcontrib>Puig, Sergi</creatorcontrib><creatorcontrib>Peñarrubia, Lola</creatorcontrib><title>Arabidopsis heavy metal P-type ATPase HMA5 interacts with metallochaperones and functions in copper detoxification of roots</title><title>The Plant journal : for cell and molecular biology</title><addtitle>Plant J</addtitle><description>Since copper (Cu) is essential in key physiological oxidation reactions, organisms have developed strategies for handling Cu while avoiding its potentially toxic effects. Among the tools that have evolved to cope with Cu is a network of Cu homeostasis factors such as Cu-transporting P-type ATPases that play a key role in transmembrane Cu transport. In this work we present the functional characterization of an Arabidopsis Cu-transporting P-type ATPase, denoted heavy metal ATPase 5 (HMA5), and its interaction with Arabidopsis metallochaperones. HMA5 is primarily expressed in roots, and is strongly and specifically induced by Cu in whole plants. We have identified and characterized plants carrying two independent T-DNA insertion alleles, hma5-1 and hma5-2. Both mutants are hypersensitive to Cu but not to other metals such as iron, zinc or cadmium. Interestingly, root tips from Cu-treated hma5 mutants exhibit a wave-like phenotype at early stages and later on main root growth completely arrests whereas lateral roots emerge near the crown. Accordingly, these lines accumulate Cu in roots to a greater extent than wild-type plants under Cu excess. Finally, yeast two-hybrid experiments demonstrate that the metal-binding domains of HMA5 interact with Arabidopsis ATX1-like Cu chaperones, and suggest a regulatory role for the plant-specific domain of the CCH Cu chaperone. Based on these findings, we propose a role for HMA5 in Cu compartmentalization and detoxification.</description><subject>Adenosine Triphosphatases - chemistry</subject><subject>Adenosine Triphosphatases - genetics</subject><subject>Adenosine Triphosphatases - metabolism</subject><subject>Agronomy. Soil science and plant productions</subject><subject>Amino Acid Sequence</subject><subject>Arabidopsis</subject><subject>Arabidopsis - enzymology</subject><subject>Arabidopsis Proteins - chemistry</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Copper - metabolism</subject><subject>Cu homeostasis</subject><subject>Cytogenetics</subject><subject>DNA Primers</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Generalities. Genetics. Plant material</subject><subject>Genes, Plant</subject><subject>Genetics and breeding of economic plants</subject><subject>heavy metal P‐type ATPase</subject><subject>HMA5</subject><subject>metal detoxification</subject><subject>metallochaperones</subject><subject>Molecular Chaperones - metabolism</subject><subject>Molecular Sequence Data</subject><subject>Plant Roots - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>Sequence Homology, Amino Acid</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV2L1DAUhoMo7rj6FzQIetearybNhRfDoq6y4oAjeBfOpKmTodPUpHVn8M-b7gwueGVuEnif9-TAgxCmpKT5vNmVlMuq4JR_LxkhVUmYJLQ8PECLv8FDtCBakkIJyi7Qk5R2hFDFpXiMLqjkUmkpF-j3MsLGN2FIPuGtg19HvHcjdHhVjMfB4eV6Bcnh68_LCvt-dBHsmPCtH7cnrgt2C4OLoXcJQ9_gdurt6EOfMo5tGHKGGzeGg2-9hTnBocUxhDE9RY9a6JJ7dr4v0fr9u_XVdXHz5cPHq-VNYSumaVE1kqpKqcYy3VLVKO20Zg1owaWjsuVaAmFCCKI3nNcst-qmtlbomoPd8Ev0-jR2iOHn5NJo9j5Z13XQuzAlw0gtBWcsgy__AXdhin1ezTDKhdaakgzVJ8jGkFJ0rRmi30M8GkrMLMfszOzAzA7MLMfcyTGHXH1-nj9t9q65L55tZODVGYBkoWsj9Nane04JRdQd9_bE3frOHf97AbNefZpfuf_i1G8hGPgR8x_fvrIcEEpqTbjkfwA7K7Pw</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Andrés-Colás, Nuria</creator><creator>Sancenón, Vicente</creator><creator>Rodríguez-Navarro, Susana</creator><creator>Mayo, Sonia</creator><creator>Thiele, Dennis J</creator><creator>Ecker, Joseph R</creator><creator>Puig, Sergi</creator><creator>Peñarrubia, Lola</creator><general>Oxford, UK : Blackwell Science Ltd</general><general>Blackwell Science Ltd</general><general>Blackwell Science</general><general>Blackwell Publishing Ltd</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>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>2006</creationdate><title>Arabidopsis heavy metal P-type ATPase HMA5 interacts with metallochaperones and functions in copper detoxification of roots</title><author>Andrés-Colás, Nuria ; Sancenón, Vicente ; Rodríguez-Navarro, Susana ; Mayo, Sonia ; Thiele, Dennis J ; Ecker, Joseph R ; Puig, Sergi ; Peñarrubia, Lola</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5291-5d617577dc29f17d79e992da9436e16f396a0244409b3382c528d8cc4983acb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adenosine Triphosphatases - chemistry</topic><topic>Adenosine Triphosphatases - genetics</topic><topic>Adenosine Triphosphatases - metabolism</topic><topic>Agronomy. Soil science and plant productions</topic><topic>Amino Acid Sequence</topic><topic>Arabidopsis</topic><topic>Arabidopsis - enzymology</topic><topic>Arabidopsis Proteins - chemistry</topic><topic>Arabidopsis Proteins - genetics</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Copper - metabolism</topic><topic>Cu homeostasis</topic><topic>Cytogenetics</topic><topic>DNA Primers</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Generalities. Genetics. Plant material</topic><topic>Genes, Plant</topic><topic>Genetics and breeding of economic plants</topic><topic>heavy metal P‐type ATPase</topic><topic>HMA5</topic><topic>metal detoxification</topic><topic>metallochaperones</topic><topic>Molecular Chaperones - metabolism</topic><topic>Molecular Sequence Data</topic><topic>Plant Roots - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>Sequence Homology, Amino Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andrés-Colás, Nuria</creatorcontrib><creatorcontrib>Sancenón, Vicente</creatorcontrib><creatorcontrib>Rodríguez-Navarro, Susana</creatorcontrib><creatorcontrib>Mayo, Sonia</creatorcontrib><creatorcontrib>Thiele, Dennis J</creatorcontrib><creatorcontrib>Ecker, Joseph R</creatorcontrib><creatorcontrib>Puig, Sergi</creatorcontrib><creatorcontrib>Peñarrubia, Lola</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>Biotechnology Research Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>The Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andrés-Colás, Nuria</au><au>Sancenón, Vicente</au><au>Rodríguez-Navarro, Susana</au><au>Mayo, Sonia</au><au>Thiele, Dennis J</au><au>Ecker, Joseph R</au><au>Puig, Sergi</au><au>Peñarrubia, Lola</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Arabidopsis heavy metal P-type ATPase HMA5 interacts with metallochaperones and functions in copper detoxification of roots</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><addtitle>Plant J</addtitle><date>2006</date><risdate>2006</risdate><volume>45</volume><issue>2</issue><spage>225</spage><epage>236</epage><pages>225-236</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>Since copper (Cu) is essential in key physiological oxidation reactions, organisms have developed strategies for handling Cu while avoiding its potentially toxic effects. Among the tools that have evolved to cope with Cu is a network of Cu homeostasis factors such as Cu-transporting P-type ATPases that play a key role in transmembrane Cu transport. In this work we present the functional characterization of an Arabidopsis Cu-transporting P-type ATPase, denoted heavy metal ATPase 5 (HMA5), and its interaction with Arabidopsis metallochaperones. HMA5 is primarily expressed in roots, and is strongly and specifically induced by Cu in whole plants. We have identified and characterized plants carrying two independent T-DNA insertion alleles, hma5-1 and hma5-2. Both mutants are hypersensitive to Cu but not to other metals such as iron, zinc or cadmium. Interestingly, root tips from Cu-treated hma5 mutants exhibit a wave-like phenotype at early stages and later on main root growth completely arrests whereas lateral roots emerge near the crown. Accordingly, these lines accumulate Cu in roots to a greater extent than wild-type plants under Cu excess. Finally, yeast two-hybrid experiments demonstrate that the metal-binding domains of HMA5 interact with Arabidopsis ATX1-like Cu chaperones, and suggest a regulatory role for the plant-specific domain of the CCH Cu chaperone. Based on these findings, we propose a role for HMA5 in Cu compartmentalization and detoxification.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Science Ltd</pub><pmid>16367966</pmid><doi>10.1111/j.1365-313X.2005.02601.x</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0960-7412
ispartof The Plant journal : for cell and molecular biology, 2006, Vol.45 (2), p.225-236
issn 0960-7412
1365-313X
language eng
recordid cdi_proquest_miscellaneous_20864322
source Wiley Free Content; MEDLINE; IngentaConnect Free/Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adenosine Triphosphatases - chemistry
Adenosine Triphosphatases - genetics
Adenosine Triphosphatases - metabolism
Agronomy. Soil science and plant productions
Amino Acid Sequence
Arabidopsis
Arabidopsis - enzymology
Arabidopsis Proteins - chemistry
Arabidopsis Proteins - genetics
Arabidopsis Proteins - metabolism
Base Sequence
Biological and medical sciences
Copper - metabolism
Cu homeostasis
Cytogenetics
DNA Primers
Fundamental and applied biological sciences. Psychology
Generalities. Genetics. Plant material
Genes, Plant
Genetics and breeding of economic plants
heavy metal P‐type ATPase
HMA5
metal detoxification
metallochaperones
Molecular Chaperones - metabolism
Molecular Sequence Data
Plant Roots - metabolism
RNA, Messenger - genetics
Sequence Homology, Amino Acid
title Arabidopsis heavy metal P-type ATPase HMA5 interacts with metallochaperones and functions in copper detoxification of roots
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T03%3A25%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Arabidopsis%20heavy%20metal%20P-type%20ATPase%20HMA5%20interacts%20with%20metallochaperones%20and%20functions%20in%20copper%20detoxification%20of%20roots&rft.jtitle=The%20Plant%20journal%20:%20for%20cell%20and%20molecular%20biology&rft.au=Andr%C3%A9s-Col%C3%A1s,%20Nuria&rft.date=2006&rft.volume=45&rft.issue=2&rft.spage=225&rft.epage=236&rft.pages=225-236&rft.issn=0960-7412&rft.eissn=1365-313X&rft_id=info:doi/10.1111/j.1365-313X.2005.02601.x&rft_dat=%3Cproquest_cross%3E20864322%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=213499910&rft_id=info:pmid/16367966&rfr_iscdi=true