MicroRNAs function as cis- and trans-acting modulators of peripheral circadian clocks |
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Authors: | Vikram R. Shende Sam-Moon Kim Nichole Neuendorff David J. Earnest |
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Affiliation: | 1. Department of Biology, Texas A&M University, College Station, TX, USA;2. Center for Biological Clocks Research, Texas A&M University, College Station, TX, USA;3. Department of Neuroscience and Experimental Therapeutics, Texas A&M Health Science Center, College of Medicine, Bryan, TX, USA |
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Abstract: | ![]() Based on their extracellular expression and targeting of the clock gene Bmal1, miR-142-3p and miR-494 were analyzed for evidence of vesicle-mediated communication between cells and intracellular functional activity. Our studies demonstrate that: miR-142-3p + miR-494 overexpression decreases endogenous BMAL1 levels, increases the period of Per2 oscillations, and increases extracellular miR-142-3p/miR-494 abundance in conditioned medium; miRNA-enriched medium increases intracellular expression of miR-142-3p and represses Bmal1 3′-UTR activity in naïve cells; and inhibitors of vesicular trafficking modulate intercellular communication of these miRNAs and ensemble Per2 rhythms. Thus, miR-142-3p and miR-494 may function as cis- and trans-acting signals contributing to local temporal coordination of cell-autonomous circadian clocks. |
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Keywords: | Circadian Pacemaker Oscillation 3&prime -UTR E-box Period 1 Period 2 Clock miRNA-recognition element |
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