Source:http://linkedlifedata.com/resource/pubmed/id/17379376
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2007-4-9
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pubmed:abstractText |
The aim of this study was to identify the di(n-butyl) phthalate (DBP)-induced differentially expressed genes (DEGs) using a novel annealing control primer system in the testes of Sprague-Dawley male rats. Animals (4 weeks of age) were administered orally either corn oil only (vehicle control) or DBP (250, 500, or 750 mg/kg/day) for 30 days. Total RNA was isolated from the rat testes and GeneFishing PCR was used to determine the differential gene expression levels. Using this technique, a total of 59 DEG mRNA fragments were observed in the testes treated with DBP 750 mg/kg/day compared to vehicle control. Of these 59 genes, 31 genes were significantly altered after exposing rats to high dose DBP (750 mg/kg/day), and their sequences cloned. Based on the Basic Local Alignment Search Tool (BLAST), 4 expressed sequence tags (EST), 27 cloned genes (Insl3, pgrp, H1SHR, etc.) and 3 genes (LDHA, lactate dehydrogenase A; Spag4, sperm associated antigen 4 and PBR, peripheral-type benzodiazepine receptor) were found to be involved in spermatogenesis and steroidogenesis. In addition, the expression patterns of the steroidogenesis-related genes such as scavenger receptor class B-1 (SR-B1), steroidogenic acute regulated protein (StAR), P450 side chain cleavage (P450scc), CYP17, and CYP19 were further analyzed by RT-PCR. Significant increases in the mRNA levels of steroidogenesis-related genes (PBR, SR-B1, StAR, P450scc, and CYP17) were observed in the high dose DBP-treated rats. However, DBP significantly decreased the CYP19 mRNA levels compared with controls. DBP (750 mg/kg/day) significantly increased the TR-alpha1 and PPARgamma expression in testes, whereas the AR and ERbeta protein levels were significantly reduced in the same group. These data indicate that the steroidogenesis- or spermatogenesis-related genes identified in this study may provide insights into the molecular mechanisms underlying environmental pollutants-mediated male infertility.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Dibutyl Phthalate,
http://linkedlifedata.com/resource/pubmed/chemical/Estrogen Receptor beta,
http://linkedlifedata.com/resource/pubmed/chemical/PPAR alpha,
http://linkedlifedata.com/resource/pubmed/chemical/Plasticizers,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Androgen
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0300-483X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
5
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pubmed:volume |
234
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
103-12
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pubmed:meshHeading |
pubmed-meshheading:17379376-Administration, Oral,
pubmed-meshheading:17379376-Age Factors,
pubmed-meshheading:17379376-Animals,
pubmed-meshheading:17379376-Blotting, Western,
pubmed-meshheading:17379376-Dibutyl Phthalate,
pubmed-meshheading:17379376-Dose-Response Relationship, Drug,
pubmed-meshheading:17379376-Estrogen Receptor beta,
pubmed-meshheading:17379376-Gene Expression Profiling,
pubmed-meshheading:17379376-Gene Expression Regulation,
pubmed-meshheading:17379376-Genes, erbA,
pubmed-meshheading:17379376-Male,
pubmed-meshheading:17379376-Organ Size,
pubmed-meshheading:17379376-PPAR alpha,
pubmed-meshheading:17379376-Plasticizers,
pubmed-meshheading:17379376-RNA, Messenger,
pubmed-meshheading:17379376-Rats,
pubmed-meshheading:17379376-Rats, Sprague-Dawley,
pubmed-meshheading:17379376-Receptors, Androgen,
pubmed-meshheading:17379376-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:17379376-Spermatogenesis,
pubmed-meshheading:17379376-Testis
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pubmed:year |
2007
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pubmed:articleTitle |
Identification of differentially expressed genes in the testis of Sprague-Dawley rats treated with di(n-butyl) phthalate.
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pubmed:affiliation |
Laboratory of Molecular Toxicology, College of Pharmacy, Pusan National University, San 30, Jangjun-Dong, Gumjung-Ku, Busan, South Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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