Complete sequence data for the RNA 3 of both citrus leaf rugose (CiLRV) and citrus variegation (CVV) ilarviruses have been determined. The RNAs are 2289 nt (CiLRV) and 2309 nt (CVV) in length and both contain the typical Bromoviridae arrangement of two open reading frames (ORFs) which, when translated, code for proteins that correspond to the M r 32 000 (32K) putative movement proteins (ORF 1) and the coat proteins (ORF 2) of the respective viruses. The 3' termini of both viruses can be folded to form a secondary structure similar to those reported for other ilarviruses. These are the first complete nucleotide sequences for RNA 3 of members of subgroup 2 of the ilarviruses. The two viruses share substantial homology in nucleic acid sequence, code for identically sized coat proteins and share high levels of identity in the translated products of both ORFs. Although related, these viruses differ sufficiently to be considered distinct. The RNA 3s of CiLRV and CVV appear to be distinct from those of other ilarviruses for which comparable sequence data are available and also from the closely related alfalfa mosaic virus.Citrus leaf rugose virus (CiLRV) and citrus variegation virus (CVV) are two serologically related but biologically distinct ilarviruses that infect citrus (Garnsey, 1975). Genomes of ilarviruses consist typically of three RNA species of approx. 3.4 kb (RNA 1), 2.9 kb (RNA 2) and 2"2 kb (RNA 3). While RNA 1 and RNA 2 are both monocistronic, RNA 3 is bicistronic with ORF 1 coding for a putative movement protein and ORF 2 coding for the viral coast protein. The coat protein gene in RNA 3 is not expressed directly but as a subgenomic, highly effective message -RNA 4 -of approx. 0"9 kb (Symons, 1985). CiLRV and CVV both have coat proteins with an M r of 26000 which are serologically related to each other (Garnsey, 1975). As groupings within the ilarviruses are based on serological relationships both are members of subgroup 2 which also includes elm mottle virus, Tulare apple mosaic virus and asparagus virus II (Francki et al., 1991).