Journal
PHYSICAL BIOLOGY
Volume 8, Issue 5, Pages -Publisher
IOP PUBLISHING LTD
DOI: 10.1088/1478-3975/8/5/055002
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Funding
- NEI NIH HHS [EY019303, R01 EY019303, R01 EY019303-01A1] Funding Source: Medline
- NIDA NIH HHS [DA027807, R01 DA027807-01, R01 DA027807] Funding Source: Medline
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Micro-RNAs (miRNAs) play a crucial role in post-transcriptional gene regulation by pairing with target mRNAs to repress protein production. It has been shown that over one-third of human genes are targeted by miRNA. Although hundreds of miRNAs have been identified in mammalian genomes, the function of miRNA-based repression in the context of gene regulation networks still remains unclear. In this study, we explore the functional roles of feedback regulation by miRNAs. In a model where repression of translation occurs by sequestration of mRNA by miRNA, we find that miRNA and mRNA levels are anti-correlated, resulting in larger fluctuation in protein levels than theoretically expected assuming no correlation between miRNA and mRNA levels. If miRNA repression is due to a catalytic suppression of translation rates, we analytically show that the protein fluctuations can be strongly repressed with miRNA regulation. We also discuss how either of these modes may be relevant for cell function.
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