Defining embryonic stem cell identity using differentiation-related microRNAs and their potential targets

被引:95
作者
Chen, Caifu
Ridzon, Dana
Lee, Chung-Tien
Blake, Julie
Sun, Yongming
Strauss, William M. [1 ]
机构
[1] Univ Colorado, MCD Biol, Boulder, CO 80309 USA
[2] Appl Biosyst Inc, R&D, Foster City, CA 94404 USA
关键词
GENE-EXPRESSION; MESSENGER-RNAS; C-ELEGANS; TRANSCRIPTION FACTOR; MOUSE; DICER; IDENTIFICATION; CANCER; LIN-14; PLURIPOTENCY;
D O I
10.1007/s00335-007-9032-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:316 / 327
页数:12
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