We completely sequenced 13,936 nucleotides (nt) of a double-stranded RNA (dsRNA) of wild rice (W-dsRNA). A single long open reading frame (13,719 nt) containing the conserved motifs of RNA-dependent RNA polymerase and RNA helicase was located in the coding strand. The identity between entire nucleotide sequence of WdsRNA and that of the dsRNA of temperate japonica rice (J-dsRNA, 13,952 nt) was 75.5%. A site-specific discontinuity (nick) was identified at nt 1,197 from the 5 end of the coding strand of W-dsRNA. This nick is also located at nt 1,211 from the 5 end in the coding strand of JdsRNA. The dsRNA copy number was increased more than 10-fold in pollen grains of both rice plants. This remarkable increase may be responsible for the highly efficient transmission of J-dsRNA via pollen that we already reported. J-dsRNA and W-dsRNA were also efficiently transmitted to interspecific F1 hybrids. Seedmediated dsRNA transmission to F2 plants was also highly efficient when the maternal parent was wild rice. The efficiency of dsRNA transmission to F2 plants was reduced when the maternal parent was temperate japonica rice; however, the reduced rates in F2 plants were returned to high levels in F3 plants.Linear large (more than 10 kb 1 ) double-stranded RNAs (dsRNAs) have frequently been identified in healthy plants such as alfalfa (1), barley (2, 3), broad bean (Vicia faba (4, 5)), cassava (6), common bean (Phaseolus vulgaris (7, 8)), pepper (9, 10) and rice (11-13). Most of these dsRNAs have no obvious effect on the phenotype of the host plant, with the exception of the dsRNA in V. faba, that is associated with cytoplasmic male sterility (4,14). These large dsRNAs are not associated with distinct virus-like particles (2, 13). They are present at a (low) constant concentration in host plants (15) and replicate using their own RNA-dependent RNA polymerase (5). Although they are usually found in the cytoplasm of host plant cells, they are effectively transmitted to progeny plants via pollen as much as by ova (2, 15). Because all attempts (mechanical inoculation, graft transmission, and aphid transmission) other than by seeds failed to transmit dsRNA to dsRNA-free plants, dsRNA is probably transmitted to progeny plants via seeds alone (2, 9, 15). Thus, these endogenous dsRNAs have some intriguing plasmid-like properties that differ from those of conventional plant RNA viruses (16).Double-stranded RNA (about 14 kb) is a feature of many strains of temperate and tropical japonica rice (cultivated rice, Oryza sativa) and of one strain of wild rice (Oryza rufipogon W-1714, an ancestor of O. sativa). It is not found in any strains of indica rice (cultivated rice, O. sativa), which rarely hybridizes with japonica rice in the field (13). These dsRNAs occur in every tissue as well as at every developmental stage, and they are transmitted very efficiently (more than 98%) to progeny plants via seeds (15). The dsRNAs are maintained at an almost constant concentration (100 copies/cell) by host plants from generation to generation (15)....