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Nucleic Acids Research Advance Access originally published online on October 2, 2008
Nucleic Acids Research 2008 36(19):6260-6268; doi:10.1093/nar/gkn511
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Nucleic Acids Research, 2008, Vol. 36, No. 19 6260-6268
© 2008 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Genomics

G-quadruplexes: the beginning and end of UTRs

Julian Leon Huppert1,*, Anthony Bugaut2, Sunita Kumari2 and Shankar Balasubramanian2

1Cavendish Laboratory, University of Cambridge, JJ Thompson Ave, Cambridge CB3 0HE and 2University Chemical Laboratory, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK

*To whom correspondence should be addressed. Tel: +44 1223 337 256; Fax: +44 1223 337 000; Email: jlh29{at}cam.ac.uk

Correspondence may also be addressed to Shankar Balasubramanian. Tel: +44 1223 336 347; Fax: +44 1223 336 913; Email: sbl0031{at}cam.ac.uk

Received April 18, 2008. Revised July 20, 2008. Accepted July 25, 2008.

Molecular mechanisms that regulate gene expression can occur either before or after transcription. The information for post-transcriptional regulation can lie within the sequence or structure of the RNA transcript and it has been proposed that G-quadruplex nucleic acid sequence motifs may regulate translation as well as transcription. Here, we have explored the incidence of G-quadruplex motifs in and around the untranslated regions (UTRs) of mRNA. We observed a significant strand asymmetry, consistent with a general depletion of G-quadruplex-forming RNA. We also observed a positional bias in two distinct regions, each suggestive of a specific function. We observed an excess of G-quadruplex motifs towards the 5'-ends of 5'-UTRs, supportive of a hypothesis linking 5'-UTR RNA G-quadruplexes to translational control. We then analysed the vicinity of 3'-UTRs and observed an over-representation of G-quadruplex motifs immediately after the 3'-end of genes, especially in those cases where another gene is in close proximity, suggesting that G-quadruplexes may be involved in the termination of gene transcription.


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