Unveiling the principle of microRNA-mediated redundancy in cellular pathway regulation

被引:59
作者
Fischer, Simon [1 ,2 ]
Handrick, Rene [1 ]
Aschrafi, Armaz [3 ]
Otte, Kerstin [1 ]
机构
[1] Univ Appl Sci Biberach, Inst Appl Biotechnol, Biberach, Germany
[2] Univ Ulm, Fac Med, D-89069 Ulm, Germany
[3] Radboud Univ Nijmegen, Dept Neuroinformat, Donders Inst Brain Funct Cognit & Behav, NL-6525 ED Nijmegen, Netherlands
关键词
chinese hamster ovary; microRNA; pathway regulation; redundancy; screen; PROGRAMMED NECROSIS; CELLS; MIRNA; PROLIFERATION; EXPRESSION; CANCER; GROWTH; RNA; TRANSFORMATION; PRODUCTIVITY;
D O I
10.1080/15476286.2015.1017238
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
Understanding the multifaceted nature of microRNA (miRNA) function in mammalian cells is still a challenge. Commonly accepted principles of cooperativity and multiplicity of miRNA function imply that individual mRNAs can be targeted by several miRNAs whereas a single miRNA may concomitantly regulate a subset of different genes. However, there is a paucity of information whether multiple miRNAs regulate critical cellular events and thereby acting redundantly. To gain insight into this notion, we conducted an unbiased high-content miRNA screen by individually introducing 1139 miRNA mimics into Chinese hamster ovary (CHO) cells. We discovered that 66% of all miRNAs significantly impacted on proliferation, protein expression, apoptosis and necrosis. In summary, we provide evidence for a substantial degree of redundancy among miRNAs to maintain cellular homeostasis.
引用
收藏
页码:238 / 247
页数:10
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