Tomato leaf curl virus (TLCV) satellite DNA (sat-DNA) is a 682 nt, circular, single-stranded molecule that lacks an open reading frame (ORF) or an apparent promoter. It contains binding motifs for the TLCV replication-associated protein, but these are dispensable for replication. To identify the regions of the sat-DNA critical for replication, the entire sequence was scanned by deletion/replacement mutagenesis. Transient assays using Nicotiana benthamiana revealed that sequences within nt 296-35 (through nt 682) are essential for replication. Sequence deletions and replacements between nt 35 and 296 were tolerated but with a significant loss of infectivity, indicating that genome size strongly influences replication efficiency. Within the permissible region, inserts of 100-700 nt were retained in transient assays although with a slight reduction in replication. In addition, sat-DNA constructs containing short non-viral DNAs replicated and spread in tobacco plants, indicating their potential as gene-delivery vectors.Plant viruses in the family Geminiviridae are characterized by small, twinned, isometric particles containing either one or two circular, single-stranded DNA species. The family comprises four genera: Mastrevirus, Curtovirus, Topocuvirus and Begomovirus, distinguished by insect vector, host range and genomic characteristics (Stanley et al., 2005). The majority of geminiviruses fall into the genus Begomovirus. Members of this genus are transmitted by the whitefly Bemisia tabaci, infect dicotyledonous plants and have either monopartite or bipartite genomes. Tomato leaf curl virus (TLCV) is a monopartite begomovirus containing a covalently closed, single-stranded DNA genome of 2766 nt that encodes six open reading frames (ORFs), two on the virion-sense strand (V1 and V2) and four on the complementary-sense strand (C1, C2, C3 and C4), interspersed by an intergenic region. The C1 ORF encodes the replication-associated protein (Rep), the only viral gene product absolutely required for virus replication.The first viral satellite associated with a DNA virus (sat-DNA) was found in TLCV-infected plants from Australia (Dry et al., 1997). This 682 nt, circular, single-stranded DNA depends on TLCV for its replication and encapsidation, but can also be supported by some other geminiviruses (Dry et al., 1997). TLCV sat-DNA does not encode any proteins and has no discernible effect on the helper virus replication or on symptom development in the hosts studied. TLCV and its sat-DNA share two copies of the sequence motif (GGTGTCT) essential for binding the viral Rep in vitro. However, mutants of both TLCV and sat-DNA impaired in Rep binding were infectious (Lin et al., 2003). These results suggested that, in contrast to other geminiviruses studied (Fontes et al., 1994;Orozco et al., 1998), TLCV and sat-DNA replication is independent of high-affinity in vitro Rep binding (Lin et al., 2003). More recently, we have observed that TLCV Rep-binding-site mutants could support the replication of both wild-type and TLCV sat-D...