Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1995-4-7
pubmed:databankReference
pubmed:abstractText
A cDNA encoding a zinc transporter (ZnT-1) was isolated from a rat kidney cDNA expression library by complementation of a mutated, zinc-sensitive BHK cell line. This cDNA was used to isolate the homologous mouse ZnT-1 gene. The proteins predicted for these transporters contain six membrane-spanning domains, a large intracellular loop and a C-terminal tail. ZnT-1 is homologous to zinc and cobalt resistance genes of yeast. Immunocytochemistry with an antibody to a myc epitope added to the C-terminus of ZnT-1 revealed localization to the plasma membrane. Transformation of normal cells with a mutant ZnT-1 lacking the first membrane-spanning domain conferred zinc sensitivity on wild-type cells, suggesting that ZnT-1 functions as a multimer. Deletion of the first two membrane-spanning domains resulted in a non-functional molecule, whereas deletion of the C-terminal tail produced a toxic phenotype. Mutant cells have a slightly higher steady-state level of intracellular zinc and high basal expression of a zinc-dependent reporter gene compared with normal cells. Mutant cells have a lower turnover of 65Zn compared with normal cells or mutant cells transformed with ZnT-1. We propose that ZnT-1 transports zinc out of cells and that its absence accounts for the increased sensitivity of mutant cells to zinc toxicity.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-1375058, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-1508175, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-1560036, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-1639868, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-1653172, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-1837150, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-2693940, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-2806412, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-2959555, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-3527054, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-3649277, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-3838360, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-3885271, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-4058587, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-708788, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-7919780, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-8026472, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-8058041, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-8065932, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-8089141, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-8108390, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-8172914, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-8242750, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-8303295, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-8419966, http://linkedlifedata.com/resource/pubmed/commentcorrection/7882967-8467794
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0261-4189
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
14
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
639-49
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:7882967-Amino Acid Sequence, pubmed-meshheading:7882967-Animals, pubmed-meshheading:7882967-Biological Transport, pubmed-meshheading:7882967-Cation Transport Proteins, pubmed-meshheading:7882967-Cell Compartmentation, pubmed-meshheading:7882967-Cell Line, pubmed-meshheading:7882967-Cloning, Molecular, pubmed-meshheading:7882967-Cricetinae, pubmed-meshheading:7882967-Gene Expression, pubmed-meshheading:7882967-Genes, pubmed-meshheading:7882967-Kidney, pubmed-meshheading:7882967-Membrane Proteins, pubmed-meshheading:7882967-Mice, pubmed-meshheading:7882967-Molecular Sequence Data, pubmed-meshheading:7882967-RNA, Messenger, pubmed-meshheading:7882967-Rats, pubmed-meshheading:7882967-Sequence Alignment, pubmed-meshheading:7882967-Sequence Homology, Nucleic Acid, pubmed-meshheading:7882967-Structure-Activity Relationship, pubmed-meshheading:7882967-Transfection, pubmed-meshheading:7882967-Zinc
pubmed:year
1995
pubmed:articleTitle
Cloning and functional characterization of a mammalian zinc transporter that confers resistance to zinc.
pubmed:affiliation
Howard Hughes Medical Institute, University of Washington, Seattle 98195.
pubmed:publicationType
Journal Article, Comparative Study