A Copper-regulated Transporter Required for Copper Acquisition, Pigmentation, and Specific Stages of Development in Drosophila melanogaster

The trace element copper is required for normal growth and development, serving as an essential catalytic co-factor for enzymes involved in energy generation, oxidative stress protection, neuropeptide maturation, and other fundamental processes. In yeast and mammals copper acquisition occurs through...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of biological chemistry 2003-11, Vol.278 (48), p.48210-48218
Hauptverfasser: Zhou, Hao, Cadigan, Ken M, Thiele, Dennis J
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 48218
container_issue 48
container_start_page 48210
container_title The Journal of biological chemistry
container_volume 278
creator Zhou, Hao
Cadigan, Ken M
Thiele, Dennis J
description The trace element copper is required for normal growth and development, serving as an essential catalytic co-factor for enzymes involved in energy generation, oxidative stress protection, neuropeptide maturation, and other fundamental processes. In yeast and mammals copper acquisition occurs through the action of the Ctr1 family of high affinity copper transporters. Here we describe studies using Drosophila melanogaster to investigate the role of copper acquisition through Ctr1 in normal growth and development. Three distinct Drosophila Ctr1 genes (Ctr1A, Ctr1B, and Ctr1C) have been identified, which have unique expression patterns over the course of development. Interestingly, Ctr1B, which is expressed exclusively during the late embryonic and larval stages of development, is transcriptionally activated in response to nutritionally induced copper deprivation and down-regulated in response to copper adequacy. The generation of Ctr1B mutant flies results in decreased larval copper accumulation, marked body pigmentation defects that parallel defects in tyrosinase activity, and specific developmental arrest under conditions of both nutritional copper limitation and excess. These studies establish that copper acquisition through the Drosophila Ctr1B transporter is crucial for normal growth and in early and specific stages of metazoan development.
doi_str_mv 10.1074/jbc.M309820200
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_19203142</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19203142</sourcerecordid><originalsourceid>FETCH-LOGICAL-c436t-89afc2e256e61b518b0abb844ca65fb7bb3fe2d10fe561cb53631b5a0439abc13</originalsourceid><addsrcrecordid>eNpFkN-L1DAQx4Mo3nr66qPkQe7JrjNJ220flz1_wYnineBbSLKTbo626SWt4t_gP22WXbghMGT45Jvhw9hrhDXCpnx_b-z6q4S2ESAAnrAVQiMLWeGvp2wFILBoRdVcsBcp3UOussXn7AJFW9fQ4Ir92_JdmCaKRaRu6fVMe34X9ZimEGeK_Ac9LD7moQvxTPKtzbPkZx_Gd_y77wYaZ3266XHPbyey3nnLb2fdUeLB8Wv6TX2YjiD3I7-OIYXp4HvNB-r1GDqd8mcv2TOn-0Svzv2S_fz44W73ubj59unLbntT2FLWc9G02llBoqqpRlNhY0Ab05Sl1XXlzMYY6UjsERxVNVpTyVpmTkMpW20sykt2dcqdYnhYKM1q8MlSnzehsCSFrQCJpcjg-gTavHCK5NQU_aDjX4WgjvpV1q8e9ecHb87Jixlo_4iffWfg7Qk4-O7wJ4tVxgd7oEGJTaPK4xEI8j-znY-U</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19203142</pqid></control><display><type>article</type><title>A Copper-regulated Transporter Required for Copper Acquisition, Pigmentation, and Specific Stages of Development in Drosophila melanogaster</title><source>MEDLINE</source><source>Free E-Journal (出版社公開部分のみ)</source><source>Alma/SFX Local Collection</source><creator>Zhou, Hao ; Cadigan, Ken M ; Thiele, Dennis J</creator><creatorcontrib>Zhou, Hao ; Cadigan, Ken M ; Thiele, Dennis J</creatorcontrib><description>The trace element copper is required for normal growth and development, serving as an essential catalytic co-factor for enzymes involved in energy generation, oxidative stress protection, neuropeptide maturation, and other fundamental processes. In yeast and mammals copper acquisition occurs through the action of the Ctr1 family of high affinity copper transporters. Here we describe studies using Drosophila melanogaster to investigate the role of copper acquisition through Ctr1 in normal growth and development. Three distinct Drosophila Ctr1 genes (Ctr1A, Ctr1B, and Ctr1C) have been identified, which have unique expression patterns over the course of development. Interestingly, Ctr1B, which is expressed exclusively during the late embryonic and larval stages of development, is transcriptionally activated in response to nutritionally induced copper deprivation and down-regulated in response to copper adequacy. The generation of Ctr1B mutant flies results in decreased larval copper accumulation, marked body pigmentation defects that parallel defects in tyrosinase activity, and specific developmental arrest under conditions of both nutritional copper limitation and excess. These studies establish that copper acquisition through the Drosophila Ctr1B transporter is crucial for normal growth and in early and specific stages of metazoan development.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M309820200</identifier><identifier>PMID: 12966081</identifier><language>eng</language><publisher>United States: American Society for Biochemistry and Molecular Biology</publisher><subject>Amino Acid Motifs ; Animals ; Animals, Genetically Modified ; Biological Transport ; Cation Transport Proteins ; Cloning, Molecular ; Copper - metabolism ; copper transporter ; Copper Transporter 1 ; Ctr1A gene ; Ctr1B gene ; Ctr1C gene ; Dose-Response Relationship, Drug ; Down-Regulation ; Drosophila melanogaster ; Drosophila melanogaster - embryology ; Drosophila Proteins - chemistry ; Drosophila Proteins - physiology ; Female ; Gene Expression Regulation, Developmental ; Genome ; Male ; Membrane Proteins - metabolism ; Membrane Proteins - physiology ; Membrane Transport Proteins - chemistry ; Membrane Transport Proteins - physiology ; Models, Genetic ; Monophenol Monooxygenase - metabolism ; Mutation ; Phenotype ; Protein Structure, Tertiary ; RNA - metabolism ; Saccharomyces cerevisiae - metabolism ; Saccharomyces cerevisiae Proteins ; Time Factors ; Transcriptional Activation</subject><ispartof>The Journal of biological chemistry, 2003-11, Vol.278 (48), p.48210-48218</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-89afc2e256e61b518b0abb844ca65fb7bb3fe2d10fe561cb53631b5a0439abc13</citedby><cites>FETCH-LOGICAL-c436t-89afc2e256e61b518b0abb844ca65fb7bb3fe2d10fe561cb53631b5a0439abc13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12966081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Hao</creatorcontrib><creatorcontrib>Cadigan, Ken M</creatorcontrib><creatorcontrib>Thiele, Dennis J</creatorcontrib><title>A Copper-regulated Transporter Required for Copper Acquisition, Pigmentation, and Specific Stages of Development in Drosophila melanogaster</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>The trace element copper is required for normal growth and development, serving as an essential catalytic co-factor for enzymes involved in energy generation, oxidative stress protection, neuropeptide maturation, and other fundamental processes. In yeast and mammals copper acquisition occurs through the action of the Ctr1 family of high affinity copper transporters. Here we describe studies using Drosophila melanogaster to investigate the role of copper acquisition through Ctr1 in normal growth and development. Three distinct Drosophila Ctr1 genes (Ctr1A, Ctr1B, and Ctr1C) have been identified, which have unique expression patterns over the course of development. Interestingly, Ctr1B, which is expressed exclusively during the late embryonic and larval stages of development, is transcriptionally activated in response to nutritionally induced copper deprivation and down-regulated in response to copper adequacy. The generation of Ctr1B mutant flies results in decreased larval copper accumulation, marked body pigmentation defects that parallel defects in tyrosinase activity, and specific developmental arrest under conditions of both nutritional copper limitation and excess. These studies establish that copper acquisition through the Drosophila Ctr1B transporter is crucial for normal growth and in early and specific stages of metazoan development.</description><subject>Amino Acid Motifs</subject><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Biological Transport</subject><subject>Cation Transport Proteins</subject><subject>Cloning, Molecular</subject><subject>Copper - metabolism</subject><subject>copper transporter</subject><subject>Copper Transporter 1</subject><subject>Ctr1A gene</subject><subject>Ctr1B gene</subject><subject>Ctr1C gene</subject><subject>Dose-Response Relationship, Drug</subject><subject>Down-Regulation</subject><subject>Drosophila melanogaster</subject><subject>Drosophila melanogaster - embryology</subject><subject>Drosophila Proteins - chemistry</subject><subject>Drosophila Proteins - physiology</subject><subject>Female</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Genome</subject><subject>Male</subject><subject>Membrane Proteins - metabolism</subject><subject>Membrane Proteins - physiology</subject><subject>Membrane Transport Proteins - chemistry</subject><subject>Membrane Transport Proteins - physiology</subject><subject>Models, Genetic</subject><subject>Monophenol Monooxygenase - metabolism</subject><subject>Mutation</subject><subject>Phenotype</subject><subject>Protein Structure, Tertiary</subject><subject>RNA - metabolism</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Saccharomyces cerevisiae Proteins</subject><subject>Time Factors</subject><subject>Transcriptional Activation</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkN-L1DAQx4Mo3nr66qPkQe7JrjNJ220flz1_wYnineBbSLKTbo626SWt4t_gP22WXbghMGT45Jvhw9hrhDXCpnx_b-z6q4S2ESAAnrAVQiMLWeGvp2wFILBoRdVcsBcp3UOussXn7AJFW9fQ4Ir92_JdmCaKRaRu6fVMe34X9ZimEGeK_Ac9LD7moQvxTPKtzbPkZx_Gd_y77wYaZ3266XHPbyey3nnLb2fdUeLB8Wv6TX2YjiD3I7-OIYXp4HvNB-r1GDqd8mcv2TOn-0Svzv2S_fz44W73ubj59unLbntT2FLWc9G02llBoqqpRlNhY0Ab05Sl1XXlzMYY6UjsERxVNVpTyVpmTkMpW20sykt2dcqdYnhYKM1q8MlSnzehsCSFrQCJpcjg-gTavHCK5NQU_aDjX4WgjvpV1q8e9ecHb87Jixlo_4iffWfg7Qk4-O7wJ4tVxgd7oEGJTaPK4xEI8j-znY-U</recordid><startdate>20031128</startdate><enddate>20031128</enddate><creator>Zhou, Hao</creator><creator>Cadigan, Ken M</creator><creator>Thiele, Dennis J</creator><general>American Society for Biochemistry and Molecular Biology</general><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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20031128</creationdate><title>A Copper-regulated Transporter Required for Copper Acquisition, Pigmentation, and Specific Stages of Development in Drosophila melanogaster</title><author>Zhou, Hao ; Cadigan, Ken M ; Thiele, Dennis J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-89afc2e256e61b518b0abb844ca65fb7bb3fe2d10fe561cb53631b5a0439abc13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Amino Acid Motifs</topic><topic>Animals</topic><topic>Animals, Genetically Modified</topic><topic>Biological Transport</topic><topic>Cation Transport Proteins</topic><topic>Cloning, Molecular</topic><topic>Copper - metabolism</topic><topic>copper transporter</topic><topic>Copper Transporter 1</topic><topic>Ctr1A gene</topic><topic>Ctr1B gene</topic><topic>Ctr1C gene</topic><topic>Dose-Response Relationship, Drug</topic><topic>Down-Regulation</topic><topic>Drosophila melanogaster</topic><topic>Drosophila melanogaster - embryology</topic><topic>Drosophila Proteins - chemistry</topic><topic>Drosophila Proteins - physiology</topic><topic>Female</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Genome</topic><topic>Male</topic><topic>Membrane Proteins - metabolism</topic><topic>Membrane Proteins - physiology</topic><topic>Membrane Transport Proteins - chemistry</topic><topic>Membrane Transport Proteins - physiology</topic><topic>Models, Genetic</topic><topic>Monophenol Monooxygenase - metabolism</topic><topic>Mutation</topic><topic>Phenotype</topic><topic>Protein Structure, Tertiary</topic><topic>RNA - metabolism</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Saccharomyces cerevisiae Proteins</topic><topic>Time Factors</topic><topic>Transcriptional Activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Hao</creatorcontrib><creatorcontrib>Cadigan, Ken M</creatorcontrib><creatorcontrib>Thiele, Dennis J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Hao</au><au>Cadigan, Ken M</au><au>Thiele, Dennis J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Copper-regulated Transporter Required for Copper Acquisition, Pigmentation, and Specific Stages of Development in Drosophila melanogaster</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2003-11-28</date><risdate>2003</risdate><volume>278</volume><issue>48</issue><spage>48210</spage><epage>48218</epage><pages>48210-48218</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>The trace element copper is required for normal growth and development, serving as an essential catalytic co-factor for enzymes involved in energy generation, oxidative stress protection, neuropeptide maturation, and other fundamental processes. In yeast and mammals copper acquisition occurs through the action of the Ctr1 family of high affinity copper transporters. Here we describe studies using Drosophila melanogaster to investigate the role of copper acquisition through Ctr1 in normal growth and development. Three distinct Drosophila Ctr1 genes (Ctr1A, Ctr1B, and Ctr1C) have been identified, which have unique expression patterns over the course of development. Interestingly, Ctr1B, which is expressed exclusively during the late embryonic and larval stages of development, is transcriptionally activated in response to nutritionally induced copper deprivation and down-regulated in response to copper adequacy. The generation of Ctr1B mutant flies results in decreased larval copper accumulation, marked body pigmentation defects that parallel defects in tyrosinase activity, and specific developmental arrest under conditions of both nutritional copper limitation and excess. These studies establish that copper acquisition through the Drosophila Ctr1B transporter is crucial for normal growth and in early and specific stages of metazoan development.</abstract><cop>United States</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>12966081</pmid><doi>10.1074/jbc.M309820200</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-9258
ispartof The Journal of biological chemistry, 2003-11, Vol.278 (48), p.48210-48218
issn 0021-9258
1083-351X
language eng
recordid cdi_proquest_miscellaneous_19203142
source MEDLINE; Free E-Journal (出版社公開部分のみ); Alma/SFX Local Collection
subjects Amino Acid Motifs
Animals
Animals, Genetically Modified
Biological Transport
Cation Transport Proteins
Cloning, Molecular
Copper - metabolism
copper transporter
Copper Transporter 1
Ctr1A gene
Ctr1B gene
Ctr1C gene
Dose-Response Relationship, Drug
Down-Regulation
Drosophila melanogaster
Drosophila melanogaster - embryology
Drosophila Proteins - chemistry
Drosophila Proteins - physiology
Female
Gene Expression Regulation, Developmental
Genome
Male
Membrane Proteins - metabolism
Membrane Proteins - physiology
Membrane Transport Proteins - chemistry
Membrane Transport Proteins - physiology
Models, Genetic
Monophenol Monooxygenase - metabolism
Mutation
Phenotype
Protein Structure, Tertiary
RNA - metabolism
Saccharomyces cerevisiae - metabolism
Saccharomyces cerevisiae Proteins
Time Factors
Transcriptional Activation
title A Copper-regulated Transporter Required for Copper Acquisition, Pigmentation, and Specific Stages of Development in Drosophila melanogaster
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T07%3A17%3A13IST&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=A%20Copper-regulated%20Transporter%20Required%20for%20Copper%20Acquisition,%20Pigmentation,%20and%20Specific%20Stages%20of%20Development%20in%20Drosophila%20melanogaster&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=Zhou,%20Hao&rft.date=2003-11-28&rft.volume=278&rft.issue=48&rft.spage=48210&rft.epage=48218&rft.pages=48210-48218&rft.issn=0021-9258&rft.eissn=1083-351X&rft_id=info:doi/10.1074/jbc.M309820200&rft_dat=%3Cproquest_cross%3E19203142%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=19203142&rft_id=info:pmid/12966081&rfr_iscdi=true