Journal of Virology, November 2008, p. 11480-11483, Vol. 82, No. 22
0022-538X/08/$08.00+0 doi:10.1128/JVI.01353-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.
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Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, Bethesda, Maryland,1 HIV Drug Resistance Program, National Cancer Institute at Frederick, Frederick, Maryland 21702-1201,2 Office of Technology Transfer, NIH, Rockville, Maryland3
Received 27 June 2008/ Accepted 22 August 2008
The two ends of RSV linear DNA are independently inserted into host DNA by integrase in vivo. We previously showed that the range of U3 sequences that are acceptable substrates for integrase appeared to be greater than the range of acceptable U5 sequences in vivo. We have done additional experiments to determine which U3 sequences are good integrase substrates. On the U3 end, there does not appear to be a stringent requirement for the canonical CA, integrase can efficiently remove three nucleotides, and six nucleotides are sufficient to allow integration with reasonable, albeit reduced, efficiency.
Published ahead of print on 3 September 2008.
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