Chen Caifu, Ridzon Dana, Lee Chung-Tien, Blake Julie, Sun Yongming, Strauss William M
R&D, Applied Biosystems, Foster City, California 94404, USA.
Mamm Genome. 2007 May;18(5):316-27. doi: 10.1007/s00335-007-9032-6. Epub 2007 Jul 3.
Defining the identity of embryonic stem (ES) cells in quantitative molecular terms is a prerequisite to understanding their functional characteristics. Little is known about the role of microRNAs (miRNAs) in the regulation of ES cell identity. Statistical analysis of miRNA expression revealed unique expression signatures that could definitively classify mouse ES (mES), embryoid bodies (mEB), and somatic tissues. Analysis of these data sets also provides further confirmation of the nonrestrictive expression of miRNAs during murine development. Using combined genome-wide expression analyses of both miRNAs and mRNAs, we observed both negative and positive correlations in gene expression between miRNAs and their predicted targets. ES-specific miRNAs were positively correlated with their predicted targets, suggesting that mES-specific miRNAs may have a different role or mechanism in regulating their targets in mES maintenance or differentiation. The concept of cellular identity has changed with technology; this study redefines cellular identity by a generic statistical method of known dimension.
从定量分子角度定义胚胎干细胞(ES细胞)的特性是理解其功能特征的前提。关于微小RNA(miRNA)在ES细胞特性调控中的作用,人们所知甚少。对miRNA表达的统计分析揭示了独特的表达特征,这些特征能够明确区分小鼠ES细胞(mES)、胚状体(mEB)和体细胞组织。对这些数据集的分析也进一步证实了miRNA在小鼠发育过程中的非限制性表达。通过对miRNA和mRNA进行全基因组联合表达分析,我们观察到miRNA与其预测靶点之间在基因表达上存在负相关和正相关。ES细胞特异性miRNA与其预测靶点呈正相关,这表明mES细胞特异性miRNA在调控mES细胞维持或分化过程中的靶点时可能具有不同的作用或机制。细胞特性的概念随着技术的发展而改变;本研究通过一种已知维度的通用统计方法重新定义了细胞特性。