Mj. Martiney et al., Selection of reversions and suppressors of a mutation in the CBF binding site of a lymphomagenic retrovirus, J VIROLOGY, 73(9), 1999, pp. 7599-7606
The retrovirus SL3 induces T-cell lymphomas in mice. The transcriptional en
hancer in the long terminal repeat (LTR) of SL3 contains two 72-bp repeats.
Each repeat contains a binding site for the transcription factor CBF (also
called AML1). The CBF binding sites are called core elements. SAA is a mut
ant that is identical to SL3 except for the presence of a single-base-pair
substitution in each of the two core elements. This mutation significantly
attenuates viral lymphomagenicity. Most lymphomas that occur in SAA-infecte
d mice contain proviruses with reversions or second-site suppressor mutatio
ns within the core element. We examined the selective pressures that might
account for the predominance of the reversions and suppressor mutations in
tumor proviruses by analyzing when proviruses with altered core sequences b
ecame abundant during the course of lymphomagenesis. Altered core sequences
were easily detected in thymus DNAs by 4 to 6 weeks after SAA infection of
mice, well before lymphomas were grossly evident. This result is consisten
t with the hypothesis that viruses with the core sequence alterations emerg
ed because they replicated more effectively in mice than SAA. The number of
72-bp tandem, repeats in the viral LTR was found to vary, presumably as a
consequence of reverse transcriptase slippage during polymerization. Provir
uses with two repeats predominated in the thymuses of SAA- and SL3-infected
mice before lymphomas developed, although LTRs with one or three repeats w
ere also present. This suggested that two was the optimal number of 72-bp r
epeats for viral replication. However, in lymphomas, proviruses with three
or four repeats usually predominated. This suggested that a late step in th
e process of lymphomagenesis led to the abundance of proviruses with additi
onal repeats. We hypothesize that proviruses with additional 72-bp repeats
endowed the cells containing them with a selective growth advantage.