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Journal of Virology, July 2006, p. 6706-6711, Vol. 80, No. 13
0022-538X/06/$08.00+0 doi:10.1128/JVI.00273-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Sayandip Mukherjee,1,2,
Yacov Ron,1 and
Joseph P. Dougherty1*
Department of Molecular Genetics, Microbiology and Immunology, Robert Wood Johnson Medical School, 675 Hoes Lane, Piscataway, New Jersey 08854,1 Graduate Program in Molecular Biosciences, Rutgers University, New Brunswick, New Jersey 089012
Received 7 February 2006/ Accepted 12 April 2006
A significant difference in the recombination rates between human immunodeficiency virus type 1 (HIV-1) and the gammaretroviruses was previously reported, with the former being 10 to 100 times more recombinogenic. It is possible that preferential copackaging of homodimers in the case of gammaretroviruses, like murine leukemia virus (MLV), led to the underestimation of their rates of recombination. To reexamine the recombination rates for MLV, experiments were performed to control for nonrandom copackaging of viral RNA, and it was found that MLV and HIV-1 exhibit similar crossover rates. The implications for control of proviral ploidy and preferential recombination during minus-strand DNA synthesis are discussed.
These authors contributed equally to the work.
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