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...
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Veröffentlicht in: | The Journal of biological chemistry 2003-11, Vol.278 (48), p.48210-48218 |
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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 |
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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> |
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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 |
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