Ciprian Gheorghe, Subburaman Mohan, Lawrence D Longo
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We analyzed and functionally annotated those genes regulated during development.</p><p><strong>Results: </strong>In comparing E10.5 to E12.5 we found that angiogenesis and fatty acid metabolism and transport related genes were up-regulated at E10.5, while genes involved in hormonal control and ribosomal proteins were up-regulated at E12.5. When comparing E12.5 to E15.5 we noted that genes involved in the cell cycle and RNA metabolism were strongly up-regulated at E12.5, while genes involved in cellular transport were up-regulated at E15.5. Finally, when comparing E15.5 to E17.5, we found genes related to cell cycle control, genes expressed in the nucleus and involved in RNA metabolism were up-regulated at E17.5.</p><p><strong>Conclusion: </strong>Microarray analysis has allowed us to describe gene expression patterns and profiles in the developing mouse placenta. Further analysis has demonstrated that several functional classes are up- and down-regulated at specific time points in placental development. These changes may have significant implications for placental development in the human.</p>","PeriodicalId":17373,"journal":{"name":"Journal of the Society for Gynecologic Investigation","volume":"13 4","pages":"256-62"},"PeriodicalIF":0.0000,"publicationDate":"2006-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jsgi.2006.02.007","citationCount":"23","resultStr":"{\"title\":\"Gene expression patterns in the developing murine placenta.\",\"authors\":\"Ciprian Gheorghe, Subburaman Mohan, Lawrence D Longo\",\"doi\":\"10.1016/j.jsgi.2006.02.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Successful placental development is crucial for optimal growth, maturation, and survival of the embryo/fetus. 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When comparing E12.5 to E15.5 we noted that genes involved in the cell cycle and RNA metabolism were strongly up-regulated at E12.5, while genes involved in cellular transport were up-regulated at E15.5. Finally, when comparing E15.5 to E17.5, we found genes related to cell cycle control, genes expressed in the nucleus and involved in RNA metabolism were up-regulated at E17.5.</p><p><strong>Conclusion: </strong>Microarray analysis has allowed us to describe gene expression patterns and profiles in the developing mouse placenta. Further analysis has demonstrated that several functional classes are up- and down-regulated at specific time points in placental development. 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引用次数: 23
摘要
目的:成功的胎盘发育对胚胎/胎儿的最佳生长、成熟和存活至关重要。为了研究胎盘发育的遗传方面,我们研究了胚胎10.5天(E10.5)、E12.5、E15.5和E17.5天小鼠胎盘的基因表达模式。方法:使用Affymetrix MU74A阵列(Affymetrix, Santa Clara, CA),我们测量了12,473个探针集的表达水平。通过两两分析,我们选择了622个探针组,对应599个基因,在E10.5和E12.5、E12.5和E15.5、E15.5和E17.5时间点之间上调或下调4倍以上。我们对发育过程中调控的基因进行了分析和功能注释。结果:对比E10.5和E12.5,我们发现血管生成和脂肪酸代谢转运相关基因在E10.5上调,而激素调控和核糖体蛋白相关基因在E12.5上调。当比较E12.5和E15.5时,我们注意到参与细胞周期和RNA代谢的基因在E12.5时被强烈上调,而参与细胞运输的基因在E15.5时被上调。最后,将E15.5与E17.5进行比较,我们发现E17.5上调了与细胞周期控制相关的基因、细胞核中表达的基因以及参与RNA代谢的基因。结论:微阵列分析使我们能够描述发育中的小鼠胎盘的基因表达模式和谱。进一步的分析表明,在胎盘发育的特定时间点,几个功能类别被上调和下调。这些变化可能对人类胎盘发育有重要影响。
Gene expression patterns in the developing murine placenta.
Objective: Successful placental development is crucial for optimal growth, maturation, and survival of the embryo/fetus. To examine genetic aspects of placental development, we investigated gene expression patterns in the murine placenta at embryonic day 10.5 (E10.5), E12.5, E15.5, and E17.5.
Methods: By use of the Affymetrix MU74A array (Affymetrix, Santa Clara, CA), we measured expression levels for 12,473 probe sets. Using pairwise analysis we selected 622 probe sets, corresponding to 599 genes, that were up- or down-regulated by more than fourfold between time points E10.5 and E12.5, E12.5 and E15.5, E15.5 and E17.5. We analyzed and functionally annotated those genes regulated during development.
Results: In comparing E10.5 to E12.5 we found that angiogenesis and fatty acid metabolism and transport related genes were up-regulated at E10.5, while genes involved in hormonal control and ribosomal proteins were up-regulated at E12.5. When comparing E12.5 to E15.5 we noted that genes involved in the cell cycle and RNA metabolism were strongly up-regulated at E12.5, while genes involved in cellular transport were up-regulated at E15.5. Finally, when comparing E15.5 to E17.5, we found genes related to cell cycle control, genes expressed in the nucleus and involved in RNA metabolism were up-regulated at E17.5.
Conclusion: Microarray analysis has allowed us to describe gene expression patterns and profiles in the developing mouse placenta. Further analysis has demonstrated that several functional classes are up- and down-regulated at specific time points in placental development. These changes may have significant implications for placental development in the human.