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首页> 外文期刊>Molecular reproduction and development >Toxicogenomic effects of neonatal exposure to diethylstilbestrol on mouse testicular gene expression in the long term: A study using cDNA microarray analysis.
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Toxicogenomic effects of neonatal exposure to diethylstilbestrol on mouse testicular gene expression in the long term: A study using cDNA microarray analysis.

机译:新生儿长期暴露于己烯雌酚对小鼠睾丸基因表达的毒物基因组学影响:一项使用cDNA微阵列分析的研究。

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We examined the effect of neonatal exposure to diethylstilbestrol (DES) on mouse testicular gene expression, using in-house mouse fetus (day 14.5) cDNA microarrays. Newborn male ICR mice were exposed to DES (50 &mgr;g/mouse/day) from neonatal day 1 to 5. Differential expression was detected in 14 genes in 4-week-old (day 28) mouse testes by cDNA microarray analysis; 11 genes (AI035263, AU080565, AU080361, AU080678, AI131681, AU080631, AA986882, AI037066, AA986537, AI156816, and AI596237) were up-regulated and three genes (AI131656, AI118968, and AI117606) were down-regulated in DES-treated mouse testes. Higher expression levels of the former eight genes, out of the up-regulated genes picked-up by the microarray, were also confirmed by reverse transcription and real-time polymerase chain reaction (real-time RT-PCR) analysis. However, the differential expression of other genes could not be confirmed. Real-time RT-PCR analysis also revealed that expression levels of the eight genes were still higher in DES-treated testes at 8 and 12 weeks of age. Our results suggest that cDNA microarray analysis is a useful method by which a large number of gene expressions are simultaneously detected and changes in gene expression are screened. In addition, our results suggest that these genes, whose expressions are changed in the testes of adult mice by fetal or neonatal exposure to exogenous chemicals, might be candidates for predictive biological markers. Mol. Reprod. Dev. 63: 17-23, 2002. Copyright 2002 Wiley-Liss, Inc.
机译:我们使用室内小鼠胎儿(第14.5天)cDNA微阵列检查了新生儿暴露于己烯雌酚(DES)对小鼠睾丸基因表达的影响。从新生儿的第1天到第5天,将新生的雄性ICR小鼠暴露于DES(50 mg /小鼠/天)。通过cDNA微阵列分析,在4周龄(第28天)的小鼠睾丸中的14个基因中检测到差异表达。 DES处理的小鼠中有11个基因(AI035263,AU080565,AU080361,AU080678,AI131681,AU080631,AA986882,AI037066,AA986537,AI156816和AI596237)被上调,而三个基因(AI131656,AI118968和AI117606)被下调。睾丸。通过逆转录和实时聚合酶链反应(实时RT-PCR)分析也证实了微阵列拾取的上调基因中前八个基因的较高表达水平。但是,无法确认其他基因的差异表达。实时RT-PCR分析还显示,在8周和12周龄的经DES处理的睾丸中,八个基因的表达水平仍然更高。我们的结果表明,cDNA微阵列分析是一种有用的方法,通过该方法可以同时检测大量基因表达并筛选基因表达的变化。此外,我们的研究结果表明,这些基因的表达在成年小鼠的睾丸中会因胎儿或新生儿暴露于外源性化学物质而发生改变,这些基因可能是预测性生物标志物的候选基因。大声笑责备。开发人员63:17-23,2002。版权所有2002 Wiley-Liss,Inc.。

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