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Endogenous RNA interference is driven by copy number.

Authors:
Cristina Cruz Jonathan Houseley

Elife 2014 Feb 11;3:e01581. Epub 2014 Feb 11.

Epigenetics Programme, The Babraham Institute, Cambridge, United Kingdom.

A plethora of non-protein coding RNAs are produced throughout eukaryotic genomes, many of which are transcribed antisense to protein-coding genes and could potentially instigate RNA interference (RNAi) responses. Here we have used a synthetic RNAi system to show that gene copy number is a key factor controlling RNAi for transcripts from endogenous loci, since transcripts from multi-copy loci form double stranded RNA more efficiently than transcripts from equivalently expressed single-copy loci. Selectivity towards transcripts from high-copy DNA is therefore an emergent property of a minimal RNAi system. The ability of RNAi to selectively degrade transcripts from high-copy loci would allow suppression of newly emerging transposable elements, but such a surveillance system requires transcription. We show that low-level genome-wide pervasive transcription is sufficient to instigate RNAi, and propose that pervasive transcription is part of a defense mechanism capable of directing a sequence-independent RNAi response against transposable elements amplifying within the genome. DOI: http://dx.doi.org/10.7554/eLife.01581.001.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918874PMC
http://dx.doi.org/10.7554/eLife.01581DOI Listing
February 2014

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