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A microRNA in a Multiple-Turnover RNAi Enzyme Complex
Abstract
In animals, the double-stranded RNA-specific endonuclease Dicer produces two classes of functionally distinct, tiny RNAs: microRNAs (miRNAs) and small interfering RNAs (siRNAs). miRNAs regulate mRNA translation, whereas siRNAs direct RNA destruction via the RNA interference (RNAi) pathway. Here we show that, in human cell extracts, the miRNA let - 7 naturally enters the RNAi pathway, which suggests that only the degree of complementarity between a miRNA and its RNA target determines its function. Human let - 7 is a component of a previously identified, miRNA-containing ribonucleoprotein particle, which we show is an RNAi enzyme complex. Each let - 7 –containing complex directs multiple rounds of RNA cleavage, which explains the remarkable efficiency of the RNAi pathway in human cells.
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Base-pairing interactions between a miRNA and its mRNA target allow targeting of the mRNA for degradation or repression of translation.
“Base-pairing interactions between the miRNA and mRNA target, allow for targeting of the mRNA for degradation or repression of translation42,46.”
From Pathways and Molecular Mechanisms Governing LDL Receptor Regulation (2025) · cites this paper as [46]
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Metadata
- Authors
- Hutvágner, G., & Zamore, P. D.
- Affiliations
- Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Lazare Research Building, Room 825, 364 Plantation Street, Worcester, MA 01605, USA.
- Venue
- Science
- Published
- 2002-09-20
- Volume
- 297
- Issue
- 5589
- Pages
- 2056-2060
- ISSN
- 0036-8075
- 1095-9203
- Cited by
- 1,674
- References
- 2
- Language
- en
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