S. Kubota et al., LONG CELLULAR REPEATS FLANKING A DEFECTIVE HTLV-I PROVIRUS - IMPLICATION FOR SITE-TARGETED INTEGRATION, Oncogene, 8(10), 1993, pp. 2873-2877
Retroviruses generally integrate as proviruses which are flanked by lo
ng-terminal repeats (LTRs) on both 5' and 3' ends. Since these LTRs ar
e required for the efficient integration mediated by the viral integra
se, it is believed that defective proviruses with a single LTR are nor
mally formed by deletion after integration. However, we found no delet
ion of cellular sequences around the integration site of such a defect
ive HTLV-1. Rather, we identified 99 bp-long direct repeats adjacent t
o both ends of the defective provirus. The repeated cellular sequences
contained a potential poly(A) signal followed by a retroviral primer-
binding-site-like sequence. The presence of the direct repeats of cell
ular sequences can be explained by the integration of the defective vi
rus through homologous recombination between cellular and viral read-t
hrough sequences.