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发育中的小鼠胎盘的基因表达模式。

Gene expression patterns in the developing murine placenta.

作者信息

Gheorghe Ciprian, Mohan Subburaman, Longo Lawrence D

机构信息

Center for Perinatal Biology, Department of Physiology, Loma Linda University, Loma Linda, California 92350, USA.

出版信息

J Soc Gynecol Investig. 2006 May;13(4):256-62. doi: 10.1016/j.jsgi.2006.02.007.

Abstract

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.

摘要

目的

成功的胎盘发育对于胚胎/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,我们调查了胚胎第10.5天(E10.5)、E12.5、E15.5和E17.5时小鼠胎盘的基因表达模式。

方法

使用Affymetrix MU74A芯片(Affymetrix,加利福尼亚州圣克拉拉),我们测量了12473个探针组的表达水平。通过成对分析,我们选择了622个探针组,对应于599个基因,这些基因在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超过四倍。我们对发育过程中调控的那些基因进行了分析和功能注释。

结果

在比较E10.5和E12.5时,我们发现血管生成以及脂肪酸代谢和转运相关基因在E10.5时上调,而参与激素控制和核糖体蛋白的基因在E12.5时上调。在比较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时强烈上调,而参与细胞转运的基因在E15.5时上调。最后,在比较E15.5和E17.5时,我们发现与细胞周期控制相关的基因、在细胞核中表达并参与RNA代谢的基因在E17.5时上调。

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概况。进一步分析表明,在胎盘发育的特定时间点,几个功能类别上调和下调。这些变化可能对人类胎盘发育具有重要意义。

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