Brar A K, Handwerger S, Kessler C A, Aronow B J
Department of Endocrinology, Children's Hospital Research Foundation, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229, USA.
Physiol Genomics. 2001 Dec 21;7(2):135-48. doi: 10.1152/physiolgenomics.00061.2001.
Gene induction and categorical reprogramming during in vitro human endometrial fibroblast decidualization. Physiol Genomics 7: 135-148, 2001. First published September 21, 2001; 10.1152/physiolgenomics.00061.2001.-Human decidual fibroblasts undergo a differentiative commitment to the acquisition of endocrine, metabolic, and structural cell functions in a process known as decidualization. Decidualization is critical for embryo implantation and placental function. We characterized gene expression pattern kinetics during decidual fibroblast differentiation by microarray analysis. Of 6,918 genes analyzed, 121 genes were induced by more than twofold, 110 were downregulated, and 50 showed biphasic behavior. Dynamically regulated genes were could be fit into nine K-means algorithm-based kinetic pattern groups, and by biologic classification, into five categories: cell and tissue function, cell and tissue structure, regulation of gene expression, expressed sequence tag (EST), and "function unknown." Reprogramming of genes within specific functional groups and gene families was a prominent feature that consisted of simultaneous induction and downregulation of a set of genes with related function. We previously observed a conceptually similar process during fetal trophoblast differentiation, in which the same phenomena applied to different genes. Of the 569 dynamically regulated genes regulated by either model, only 81 of these were in common. These results suggest that reprogramming of gene expression within focused functional categories represents a fundamental aspect of cellular differentiation.
体外人子宫内膜成纤维细胞蜕膜化过程中的基因诱导和类别重编程。《生理基因组学》7: 135 - 148, 2001年。首次发表于2001年9月21日;10.1152/physiolgenomics.00061.2001。- 人蜕膜成纤维细胞在一个被称为蜕膜化的过程中经历分化,获得内分泌、代谢和结构细胞功能。蜕膜化对胚胎着床和胎盘功能至关重要。我们通过微阵列分析表征了蜕膜成纤维细胞分化过程中的基因表达模式动力学。在分析的6918个基因中,121个基因被诱导超过两倍,110个基因被下调,50个基因表现出双相行为。动态调节的基因可分为基于K均值算法的九个动力学模式组,按生物学分类可分为五类:细胞和组织功能、细胞和组织结构、基因表达调控、表达序列标签(EST)和“功能未知”。特定功能组和基因家族内基因的重编程是一个突出特征,包括一组相关功能基因的同时诱导和下调。我们之前在胎儿滋养层细胞分化过程中观察到一个概念上类似的过程,其中相同的现象适用于不同的基因。在这两种模型调节的569个动态调节基因中,只有81个是相同的。这些结果表明,特定功能类别内基因表达的重编程是细胞分化的一个基本方面。