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Identification of Mouse SLC39A8 as the Transporter Responsible for Cadmium-Induced Toxicity in the Testis
Testicular necrosis is a sensitive endpoint for cadmium ( Cd2+, Cd) toxicity across all species tested. Resistance to Cd-induced testicular damage is a recessive trait assigned to the Cdm locus on mouse chromosome 3. We first narrowed the Cdm-gene-containing region to 880 kb. SNP analysis of this re...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2005-03, Vol.102 (9), p.3401-3406 |
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creator | Dalton, Timothy P. He, Lei Wang, Bin Miller, Marian L. Jin, Li Stringer, Keith F. Chang, Xiaoqing Baxter, C. Stuart Nebert, Daniel W. Palmiter, Richard D. |
description | Testicular necrosis is a sensitive endpoint for cadmium ( Cd2+, Cd) toxicity across all species tested. Resistance to Cd-induced testicular damage is a recessive trait assigned to the Cdm locus on mouse chromosome 3. We first narrowed the Cdm-gene-containing region to 880 kb. SNP analysis of this region from two sensitive and two resistant inbred strains demonstrated a 400-kb haplotype block consistent with the Cd-induced toxicity phenotype; in this region is the Slc39a8 gene encoding a member of the solute-carrier superfamily. Slc39a8 encodes SLC39A8 (ZIP8), whose homologs in plant and yeast are putative zinc transporters. We show here that ZRT-, IRT-like protein (ZIP)8 expression in cultured mouse fetal fibroblasts leads to a >10-fold increase in the rate of intracellular Cd influx and accumulation and 30-fold increase in sensitivity to Cd-induced cell death. The complete ZIP8 mRNA and intron-exon splice junctions have no nucleotide differences between two sensitive and two resistant strains of mice; by using situ hybridization, we found that ZIP8 mRNA is prominent in the vascular endothelial cells of the testis of the sensitive strains of mice but absent in these cells of resistant strains. Slc39a8 is therefore the Cdm gene, defining sensitivity to Cd toxicity specifically in vascular endothelial cells of the testis. |
doi_str_mv | 10.1073/pnas.0406085102 |
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Stuart ; Nebert, Daniel W. ; Palmiter, Richard D.</creator><creatorcontrib>Dalton, Timothy P. ; He, Lei ; Wang, Bin ; Miller, Marian L. ; Jin, Li ; Stringer, Keith F. ; Chang, Xiaoqing ; Baxter, C. Stuart ; Nebert, Daniel W. ; Palmiter, Richard D.</creatorcontrib><description>Testicular necrosis is a sensitive endpoint for cadmium ( Cd2+, Cd) toxicity across all species tested. Resistance to Cd-induced testicular damage is a recessive trait assigned to the Cdm locus on mouse chromosome 3. We first narrowed the Cdm-gene-containing region to 880 kb. SNP analysis of this region from two sensitive and two resistant inbred strains demonstrated a 400-kb haplotype block consistent with the Cd-induced toxicity phenotype; in this region is the Slc39a8 gene encoding a member of the solute-carrier superfamily. Slc39a8 encodes SLC39A8 (ZIP8), whose homologs in plant and yeast are putative zinc transporters. We show here that ZRT-, IRT-like protein (ZIP)8 expression in cultured mouse fetal fibroblasts leads to a >10-fold increase in the rate of intracellular Cd influx and accumulation and 30-fold increase in sensitivity to Cd-induced cell death. The complete ZIP8 mRNA and intron-exon splice junctions have no nucleotide differences between two sensitive and two resistant strains of mice; by using situ hybridization, we found that ZIP8 mRNA is prominent in the vascular endothelial cells of the testis of the sensitive strains of mice but absent in these cells of resistant strains. Slc39a8 is therefore the Cdm gene, defining sensitivity to Cd toxicity specifically in vascular endothelial cells of the testis.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0406085102</identifier><identifier>PMID: 15722412</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Alternative Splicing ; Animals ; Antibodies ; Base Sequence ; Biological Sciences ; Blotting, Northern ; Blotting, Western ; Cadmium - toxicity ; Cation Transport Proteins - genetics ; Cation Transport Proteins - metabolism ; Cell lines ; Cloning, Molecular ; DNA Primers ; DNA, Complementary ; Endothelial cells ; Exons ; Genes ; Immunohistochemistry ; In Situ Hybridization ; Inbred strains ; Male ; Medical research ; Messenger RNA ; Metals ; Mice ; Proteins ; Rodents ; Sertoli cells ; Testes ; Testis - drug effects ; Testis - metabolism ; Toxicity</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2005-03, Vol.102 (9), p.3401-3406</ispartof><rights>Copyright 1993/2005 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Mar 1, 2005</rights><rights>Copyright © 2005, The National Academy of Sciences 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c590t-687ab4a3ac9e2213b743b7d67abfffeb0a1711c2a8dab0db5b95b75b8bc4cf5d3</citedby><cites>FETCH-LOGICAL-c590t-687ab4a3ac9e2213b743b7d67abfffeb0a1711c2a8dab0db5b95b75b8bc4cf5d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/102/9.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3374938$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3374938$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15722412$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dalton, Timothy P.</creatorcontrib><creatorcontrib>He, Lei</creatorcontrib><creatorcontrib>Wang, Bin</creatorcontrib><creatorcontrib>Miller, Marian L.</creatorcontrib><creatorcontrib>Jin, Li</creatorcontrib><creatorcontrib>Stringer, Keith F.</creatorcontrib><creatorcontrib>Chang, Xiaoqing</creatorcontrib><creatorcontrib>Baxter, C. Stuart</creatorcontrib><creatorcontrib>Nebert, Daniel W.</creatorcontrib><creatorcontrib>Palmiter, Richard D.</creatorcontrib><title>Identification of Mouse SLC39A8 as the Transporter Responsible for Cadmium-Induced Toxicity in the Testis</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Testicular necrosis is a sensitive endpoint for cadmium ( Cd2+, Cd) toxicity across all species tested. Resistance to Cd-induced testicular damage is a recessive trait assigned to the Cdm locus on mouse chromosome 3. We first narrowed the Cdm-gene-containing region to 880 kb. SNP analysis of this region from two sensitive and two resistant inbred strains demonstrated a 400-kb haplotype block consistent with the Cd-induced toxicity phenotype; in this region is the Slc39a8 gene encoding a member of the solute-carrier superfamily. Slc39a8 encodes SLC39A8 (ZIP8), whose homologs in plant and yeast are putative zinc transporters. We show here that ZRT-, IRT-like protein (ZIP)8 expression in cultured mouse fetal fibroblasts leads to a >10-fold increase in the rate of intracellular Cd influx and accumulation and 30-fold increase in sensitivity to Cd-induced cell death. The complete ZIP8 mRNA and intron-exon splice junctions have no nucleotide differences between two sensitive and two resistant strains of mice; by using situ hybridization, we found that ZIP8 mRNA is prominent in the vascular endothelial cells of the testis of the sensitive strains of mice but absent in these cells of resistant strains. Slc39a8 is therefore the Cdm gene, defining sensitivity to Cd toxicity specifically in vascular endothelial cells of the testis.</description><subject>Alternative Splicing</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Base Sequence</subject><subject>Biological Sciences</subject><subject>Blotting, Northern</subject><subject>Blotting, Western</subject><subject>Cadmium - toxicity</subject><subject>Cation Transport Proteins - genetics</subject><subject>Cation Transport Proteins - metabolism</subject><subject>Cell lines</subject><subject>Cloning, Molecular</subject><subject>DNA Primers</subject><subject>DNA, Complementary</subject><subject>Endothelial cells</subject><subject>Exons</subject><subject>Genes</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>Inbred strains</subject><subject>Male</subject><subject>Medical research</subject><subject>Messenger RNA</subject><subject>Metals</subject><subject>Mice</subject><subject>Proteins</subject><subject>Rodents</subject><subject>Sertoli cells</subject><subject>Testes</subject><subject>Testis - drug effects</subject><subject>Testis - metabolism</subject><subject>Toxicity</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp9kUtvEzEUhS0EoqGwZoOQxYKupr1-zMMLFlXEI1IQEoS1ZXts6mhmHGwPav99HSVqCgsWli37O0fn-iD0msAlgZZd7SaVLoFDA11NgD5BCwKCVA0X8BQtAGhbdZzyM_QipS0AiLqD5-iM1C2lnNAF8qveTtk7b1T2YcLB4a9hThb_WC-ZuO6wSjjfWLyJakq7ELON-Lstpyl5PVjsQsRL1Y9-HqvV1M_G9ngTbr3x-Q776aC1Kfv0Ej1zakj21XE_Rz8_fdwsv1Trb59Xy-t1ZWoBuWq6VmmumDLCUkqYbnlZfVNunXNWgyItIYaqrlcael1rUeu21p023Li6Z-fow8F3N-vR9qaMF9Ugd9GPKt7JoLz8-2XyN_JX-CPrmgpoiv79UR_D77lEl6NPxg6Dmmz5GUnajnaMQwHf_QNuwxynMpukQBgXhO_drg6QiSGlaN1DEAJyX6HcVyhPFRbF28f5T_yxs0fAXnmyo1LIkosU4OK_gHTzMGR7mwv55kBuUw7xAWWs5YJ17B7th7qp</recordid><startdate>20050301</startdate><enddate>20050301</enddate><creator>Dalton, Timothy P.</creator><creator>He, Lei</creator><creator>Wang, Bin</creator><creator>Miller, Marian L.</creator><creator>Jin, Li</creator><creator>Stringer, Keith F.</creator><creator>Chang, Xiaoqing</creator><creator>Baxter, C. 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Stuart</au><au>Nebert, Daniel W.</au><au>Palmiter, Richard D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of Mouse SLC39A8 as the Transporter Responsible for Cadmium-Induced Toxicity in the Testis</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2005-03-01</date><risdate>2005</risdate><volume>102</volume><issue>9</issue><spage>3401</spage><epage>3406</epage><pages>3401-3406</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Testicular necrosis is a sensitive endpoint for cadmium ( Cd2+, Cd) toxicity across all species tested. Resistance to Cd-induced testicular damage is a recessive trait assigned to the Cdm locus on mouse chromosome 3. We first narrowed the Cdm-gene-containing region to 880 kb. SNP analysis of this region from two sensitive and two resistant inbred strains demonstrated a 400-kb haplotype block consistent with the Cd-induced toxicity phenotype; in this region is the Slc39a8 gene encoding a member of the solute-carrier superfamily. Slc39a8 encodes SLC39A8 (ZIP8), whose homologs in plant and yeast are putative zinc transporters. We show here that ZRT-, IRT-like protein (ZIP)8 expression in cultured mouse fetal fibroblasts leads to a >10-fold increase in the rate of intracellular Cd influx and accumulation and 30-fold increase in sensitivity to Cd-induced cell death. The complete ZIP8 mRNA and intron-exon splice junctions have no nucleotide differences between two sensitive and two resistant strains of mice; by using situ hybridization, we found that ZIP8 mRNA is prominent in the vascular endothelial cells of the testis of the sensitive strains of mice but absent in these cells of resistant strains. Slc39a8 is therefore the Cdm gene, defining sensitivity to Cd toxicity specifically in vascular endothelial cells of the testis.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>15722412</pmid><doi>10.1073/pnas.0406085102</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alternative Splicing Animals Antibodies Base Sequence Biological Sciences Blotting, Northern Blotting, Western Cadmium - toxicity Cation Transport Proteins - genetics Cation Transport Proteins - metabolism Cell lines Cloning, Molecular DNA Primers DNA, Complementary Endothelial cells Exons Genes Immunohistochemistry In Situ Hybridization Inbred strains Male Medical research Messenger RNA Metals Mice Proteins Rodents Sertoli cells Testes Testis - drug effects Testis - metabolism Toxicity |
title | Identification of Mouse SLC39A8 as the Transporter Responsible for Cadmium-Induced Toxicity in the Testis |
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