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F9胚胎癌细胞分化为滋养层内胚层过程中的全基因组表达模式。

Global gene expression patterns during differentiation of F9 embryonal carcinoma cells into parietal endoderm.

作者信息

Harris Thomas M, Childs Geoffrey

机构信息

Department of Molecular Genetics, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.

出版信息

Funct Integr Genomics. 2002 Aug;2(3):105-19. doi: 10.1007/s10142-002-0062-6. Epub 2002 Jun 5.

Abstract

Expression levels of over 8,900 murine genes were examined, using cDNA microarrays, during the differentiation of F9 cells into parietal endoderm following exposure to retinoic acid/dibutyryl cAMP. Gene induction and repression over the time course exhibited a biphasic pattern consistent with a transition from undifferentiated F9 cells to primitive endoderm and finally parietal endoderm. A 6-h induction with retinoic acid/cAMP/cycloheximide resulted in 109 candidate immediate response genes. During a 9-day time course 516 genes were selected as being significantly induced/repressed. Several of these genes had been previously identified as having altered expression patterns in F9 cells undergoing differentiation by retinoic acid/cAMP. Functional characterization of these genes demonstrated that the majority were transcription factors while others included surface antigens and genes involved in intracellular transport. Cluster analysis, utilizing both a hierarchical algorithm and self-organizing map, resulted in very similar gene clusters. Our studies revealed an extremely complex set of interacting signals that decide between cell death, differentiation, cell cycle withdrawal, and ultimately the traits associated with the terminal differentiated parietal endoderm cell type. The sets of genes identified here can now be modulated in a rational way to try to understand their role in differentiation.

摘要

利用cDNA微阵列检测了8900多个小鼠基因在视黄酸/二丁酰环磷腺苷诱导F9细胞分化为壁内胚层过程中的表达水平。在整个时间进程中,基因的诱导和抑制呈现出双相模式,这与未分化的F9细胞向原始内胚层进而最终向壁内胚层的转变相一致。用视黄酸/环磷腺苷/环己酰亚胺诱导6小时产生了109个候选即时反应基因。在9天的时间进程中,516个基因被选为有显著诱导/抑制作用的基因。其中一些基因先前已被确定在经视黄酸/环磷腺苷诱导分化的F9细胞中表达模式发生了改变。对这些基因的功能表征表明,大多数是转录因子,而其他包括表面抗原和参与细胞内运输的基因。利用层次算法和自组织映射进行的聚类分析产生了非常相似的基因簇。我们的研究揭示了一组极其复杂的相互作用信号,这些信号决定了细胞死亡、分化、细胞周期停滞,以及最终与终末分化的壁内胚层细胞类型相关的特征。现在可以合理地调节这里鉴定出的基因集,以试图了解它们在分化中的作用。

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