Mature seed-derived calli from two elite Chinese Japonica rice (Oryza sativ
a L.) cultivars Eyi 105 and Ewan 5 were co-transformed with two plasmids, p
WRG1515 and pRSSGNA1, containing the selectable marker hygromycin phosphotr
ansferase gene (hpt), the reporter beta -glu-curonidase gene (gusA) and the
snowdrop (Galanthus nivalis) lectin gene (gna) via particle bombardment. 6
1 independent transgenic rice plants were regenerated from 329 bombarded ca
lli. 79% transgenic plants contained all the three genes, revealed by PCR/S
outhern blot analysis. Western blot analysis revealed that 36 out of 48 gna
-containing transgenic plants expressed GNA (75%) at various levels with th
e highest expression being approximately 0.5% of total soluble protein. Gen
etic analysis confirmed Mendelian segregation of transgenes in progeny. Fro
m the R2 generations whose R1 parent plants showing 3:1 Mendelian segregati
on patterns, we identified five independent homozygous lines containing and
expressing all the three transgenes. Insect bioassay and feeding tests sho
wed that these homozygous lines had significant inhibition to rice brown pl
anthopper (Nilaparvata lugens, BPH) by decreasing BPH survival and overall
fecundity, retarding BPH development and declining BPH feeding. These BPH-r
esistant lines have been incorporated into rice insect resistance breeding
program. This is the first report that homozygous transgenic rice lines exp
ressing GNA, developed by genetic transformation and through genetic analys
is-based selection, conferred enhanced resistance to BPH, one of the most d
amaging insect pests in rice.