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Journal of Virology, April 2007, p. 3652-3656, Vol. 81, No. 7
0022-538X/07/$08.00+0 doi:10.1128/JVI.02105-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Experimental Hematology, Hannover Medical School, D-30625 Hanover, Germany
Received 26 September 2006/ Accepted 5 January 2007
Alternative splicing has been recognized as a major mechanism for creating proteomic diversity from a limited number of genes. However, not all determinants regulating this process have been characterized. Using subviral human immunodeficiency virus (HIV) env constructs we observed an enhanced splicing of the RNA when expression was under control of the cytomegalovirus (CMV) promoter instead of the HIV long terminal repeat (LTR). We extended these observations to LTR- or CMV-driven murine leukemia proviruses, suggesting that retroviral LTRs are adapted to inefficient alternative splicing at most sites in order to maintain balanced gene expression.
Published ahead of print on 17 January 2007.
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