MBE Advance Access originally published online on November 4, 2008
Molecular Biology and Evolution 2009 26(2):327-334; doi:10.1093/molbev/msn249
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Research Articles |
Using Alu Elements as Polyadenylation Sites: A Case of Retroposon Exaptation


* Institut de Génétique et Microbiologie, Université Paris-Sud 11, CNRS UMR 8621, Orsay, France
Key Laboratory of Gene Engineering of the Ministry of Education, State Key Laboratory for Biocontrol, Zhongshan University, Guangzhou, People's republic of China
Kazusa DNA Research Institute, Kisarazu, Chiba, Japan
E-mail: daniel.gautheret{at}u-psud.fr.
Accepted for publication October 27, 2008.
Of the 1.1 million Alu retroposons in the human genome, about 10,000 are inserted in the 3' untranslated regions (UTR) of protein-coding genes and 1% of these (107 events) are active as polyadenylation sites (PASs). Strikingly, although Alus in 3' UTR are indifferently inserted in the forward or reverse direction, 99% of polyadenylation-active Alu sequences are forward oriented. Consensus Alu+ sequences contain sites that can give rise to polyadenylation signals and enhancers through a few point mutations. We found that the strand bias of polyadenylation-active Alus reflects a radical difference in the fitness of sense and antisense Alus toward cleavage/polyadenylation activity. In contrast to previous beliefs, Alu inserts do not necessarily represent weak or cryptic PASs; instead, they often constitute the major or the unique PAS in a gene, adding to the growing list of Alu exaptations. Finally, some Alu-borne PASs are intronic and produce truncated transcripts that may impact gene function and/or contribute to gene remodeling.
Key Words: polyadenylation retroposons Alu SINE
Dan Graur, Associate Editor