Transcripts Targeted by the MicroRNA-16 Family Cooperatively Regulate Cell Cycle Progression

Peter S. Linsley(Rosetta Stone (United States)), Janell M. Schelter(Rosetta Stone (United States)), Julja Burchard(Rosetta Stone (United States)), Miho Kibukawa(Rosetta Stone (United States)), Melissa M. Martin(Rosetta Stone (United States)), Steven R. Bartz(Rosetta Stone (United States)), Jason M. Johnson(Rosetta Stone (United States)), Jordan M. Cummins(Howard Hughes Medical Institute), Christopher K. Raymond(Rosetta Stone (United States)), Hongyue Dai(Rosetta Stone (United States)), Nelson Chau(Rosetta Stone (United States)), Michele A. Cleary(Rosetta Stone (United States)), Aimee L. Jackson(Rosetta Stone (United States)), Michael Carleton(Rosetta Stone (United States)), Lee P. Lim(Rosetta Stone (United States))
Molecular and Cellular Biology
January 22, 2007
Cited by 558Open Access
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Abstract

microRNAs (miRNAs) are abundant, approximately 21-nucleotide, noncoding regulatory RNAs. Each miRNA may regulate hundreds of mRNA targets, but the identities of these targets and the processes they regulate are poorly understood. Here we have explored the use of microarray profiling and functional screening to identify targets and biological processes triggered by the transfection of human cells with miRNAs. We demonstrate that a family of miRNAs sharing sequence identity with miRNA-16 (miR-16) negatively regulates cellular growth and cell cycle progression. miR-16-down-regulated transcripts were enriched with genes whose silencing by small interfering RNAs causes an accumulation of cells in G(0)/G(1). Simultaneous silencing of these genes was more effective at blocking cell cycle progression than disruption of the individual genes. Thus, miR-16 coordinately regulates targets that may act in concert to control cell cycle progression.


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