Selection of reversions and suppressors of a mutation in the CBF binding site of a lymphomagenic retrovirus

Citation
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
Citations number
30
Categorie Soggetti
Microbiology
Journal title
JOURNAL OF VIROLOGY
ISSN journal
0022538X → ACNP
Volume
73
Issue
9
Year of publication
1999
Pages
7599 - 7606
Database
ISI
SICI code
0022-538X(199909)73:9<7599:SORASO>2.0.ZU;2-X
Abstract
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.