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J. Virol., Sep 1996, 5998-6011, Vol 70, No. 9
C Tabernero, AS Zolotukhin, A Valentin, GN Pavlakis and BK Felber
It was previously shown that a 240-nucleotide (nt) RNA element (cis- acting
transactivation element [CTE]) located between the env gene and the 3' long
terminal repeat of simian retrovirus type 1 (SRV-1) can functionally
replace posttranscriptional activation directed by Rev and the
Rev-responsive element (RRE) when inserted into a Rev- and RRE- deficient
molecular clone of human immunodeficiency virus type 1, resulting in
efficient virus replication. Here, we analyze the molecular and structural
requirements for function of this RNA element. Deletion mutagenesis
demonstrated that the core element spans 173 nt. SRV-2 and Mason-Pfizer
monkey virus have highly homologous elements, which function similarly when
inserted into the Rev/RRE-deficient human immunodeficiency virus type 1.
Computer prediction indicated that the core CTEs of all three viruses have
similar extensive secondary structures. Mutagenesis of the SRV-1 CTE
revealed that both sequence and secondary structure are essential for
function. Nuclease probing of the SRV-1 CTE further supported the genetic
analysis and confirmed the predicted structural features of the RNA
element. Sequence analysis of the 240-nt SRV-1 CTE, after continuous
long-term propagation of the Rev- independent viruses, revealed that the
genetically defined core element remained unchanged, while regions outside
the core CTE underwent deletions or duplications. These data further
support our in vitro mutagenesis data and demonstrate the importance of the
sequence and structure of the SRV-1 CTE for appropriate function.
Copyright © 1996, American Society for Microbiology
The posttranscriptional control element of the simian retrovirus type 1 forms an extensive RNA secondary structure necessary for its function
Human Retrovirus Pathogenesis Group, ABL-Basic Research Program, National Cancer Institute-Frederick Cancer Research and Development Center, Maryland 21702-1201, USA.
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