Literature DB >> 16764866

Mismatched siRNAs downregulate mRNAs as a function of target site location.

Scott E Martin1, Natasha J Caplen.   

Abstract

In mammalian cells, RNA interference can be mediated by synthetic duplex RNAs, termed small interfering RNAs (siRNAs), which assist in cleaving completely complementary mRNA transcripts. MicroRNAs (miRNAs) are endogenous small RNAs that assist in translationally repressing mRNAs with regions of partial complementarity, but may also reduce transcript levels. Since miRNAs predominantly interact with the 3' UTRs of transcripts, we sought to ask if mismatched siRNAs mimicking miRNAs affect cognate mRNA levels as a function of target site location. We find that mismatched siRNAs targeting the 3' UTRs of two endogenous transcripts yield a greater reduction in mRNA levels than those targeting the coding region. Our findings demonstrate the importance of target site location within endogenous mRNAs for small RNAs associated with RNAi.

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Year:  2006        PMID: 16764866     DOI: 10.1016/j.febslet.2006.05.056

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  10 in total

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7.  Pilocarpine-induced seizures trigger differential regulation of microRNA-stability related genes in rat hippocampal neurons.

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9.  Multiplexing siRNAs to compress RNAi-based screen size in human cells.

Authors:  Scott E Martin; Tamara L Jones; Cheryl L Thomas; Philip L Lorenzi; Dac A Nguyen; Timothy Runfola; Michele Gunsior; John N Weinstein; Paul K Goldsmith; Eric Lader; Konrad Huppi; Natasha J Caplen
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  10 in total

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