Source:http://linkedlifedata.com/resource/pubmed/id/12856169
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2003-8-25
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pubmed:abstractText |
The imprinted multimembrane-spanning polyspecific transporter-like gene 1 ( IMPT1) encodes a predicted protein with organic cation transport capabilities. As a first step in understanding the function of IMPT1, we identified the renal structures expressing this gene in knockout mice with adenine phosphoribosyltransferase (APRT) deficiency and 2,8-dihydroxyadenine (DHA) nephrolithiasis. IMPT1 mRNA was not detected using a standard in situ hybridization (ISH) protocol, but we observed intense staining in cortico-medullary tubules and glomeruli in wild-type mice using an improved reverse transcription-polymerase chain reaction (RT-PCR) ISH procedure. IMPT1 mRNA expression was significantly decreased in the cortical region in kidney sections from APRT-deficient male mice. APRT-deficient female mice are less severely affected by DHA-induced kidney stone disease, and we observed only a modest reduction in IMPT1 expression in kidneys from these mice. IMPT1 expression in APRT heterozygous mice was comparable to that in wild-type mice, suggesting imprinting of one of the parental alleles. These findings suggest that decreased IMPT1 mRNA expression may contribute to the impaired renal function in APRT-deficient male mice, and that RT-PCR ISH is a valuable tool for localizing the site of expression of transcripts that are not detectable using standard ISH procedures.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/2,8-dihydroxyadenine,
http://linkedlifedata.com/resource/pubmed/chemical/Adenine,
http://linkedlifedata.com/resource/pubmed/chemical/Adenine Phosphoribosyltransferase,
http://linkedlifedata.com/resource/pubmed/chemical/Organic Cation Transport Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/SLC22A18 protein, human
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0300-5623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
257-61
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:12856169-Adenine,
pubmed-meshheading:12856169-Adenine Phosphoribosyltransferase,
pubmed-meshheading:12856169-Animals,
pubmed-meshheading:12856169-Biological Transport,
pubmed-meshheading:12856169-Female,
pubmed-meshheading:12856169-Gene Dosage,
pubmed-meshheading:12856169-Gene Expression,
pubmed-meshheading:12856169-Genomic Imprinting,
pubmed-meshheading:12856169-Kidney Calculi,
pubmed-meshheading:12856169-Male,
pubmed-meshheading:12856169-Mice,
pubmed-meshheading:12856169-Mice, Knockout,
pubmed-meshheading:12856169-Organic Cation Transport Proteins
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pubmed:year |
2003
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pubmed:articleTitle |
Impaired expression of an organic cation transporter, IMPT1, in a knockout mouse model for kidney stone disease.
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pubmed:affiliation |
Department of Genetics, Rutgers University, 604 Allison Road, NJ 08854-8082, Piscataway, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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