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Contents - Faperta

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172 Biotechnological Approaches for Pest Management and Ecological Sustainability<br />

Rice<br />

The complete genetic linkage map of rice was published by the end of the twentieth<br />

century (Kurata et al., 1994, 1997; Palevitz, 2000), can be used for identifi cation of<br />

genomic regions associated with resistance to insects. Considerable progress has<br />

been made in identifi cation of molecular markers/QTLs associated with resistance to<br />

insect pests in rice. Several RAPD markers linked to yellow stem borer, S. incertulas<br />

resistance have been identifi ed; the chromosome location of these genes is unknown<br />

(Selvi et al., 2002).<br />

Much progress has been made in tagging and mapping the genes conferring resistance<br />

to rice gall midge, O. oryzae. Resistance to O. oryzae is linked with RG329 (1.3 cM) and<br />

RG476 (3.4 cM) markers on chromosome 4 (Mohan et al., 1994). RAPD fragment F8 1700 is<br />

associated with susceptibility and F10 600 with resistance to O. oryzae (Nair et al., 1995),<br />

while RAPD fragment E20 570 is associated with resistance and E20 583 with susceptibility to<br />

gall midge (Nair et al., 1996). Behura et al. (2000) reported an AFLP marker, which is amplifi<br />

ed in biotypes 1, 2, and 5 of rice gall midge, but not in biotype 4. The former are avirulent<br />

on hosts bearing the Gm2 resistance gene (e.g., Phalguna), while biotype 4 is avirulent to<br />

hosts with Gm2 gene. Avirulence to Gm2 gene is sex-linked. An AFLP marker SA598 linked<br />

to Gm7, conferring resistance to biotypes 1, 2, and 4, has also been identifi ed (Sardesai<br />

et al., 2002). Gm7 is a dominant gene and is nonallelic to Gm2. A dominant resistance gene,<br />

Gm1, has been tagged and mapped on chromosome 9 (Biradar et al., 2004). The SSR markers<br />

RM316, RM444, and RM219 located on chromosome 9 are linked to Gm1 at genetic<br />

distances of 8.0, 4.9, and 5.9 cM, respectively. Gm8 has been tagged and mapped on the rice<br />

chromosome 8 ( Jain et al., 2004). Two fragments, AR257 and AS168, were linked to the<br />

resistant and susceptible phenotypes, respectively. Another resistant phenotype-specifi c<br />

marker, AP19(587) was also identifi ed using RAPDs. There is a tight linkage between the<br />

markers and the Gm8 locus. Many of these markers can be used in MAS to develop rice<br />

cultivars with resistance to gall midge.<br />

For brown planthopper, N. lugens, genomic regions on chromosomes 3 and 4 contain<br />

genes for resistance (Z. Huang et al., 2001). Two QTLs are associated with resistance to<br />

N. lugens (Alam and Cohen, 1998), of which one QTL is linked to antixenosis and second to<br />

tolerance. In another population, Xu et al. (2002) found that a main effect QTL for N. lugens<br />

resistance maps to the vicinity of a major rice gene controlling leaf and stem pubescence,<br />

suggesting that this QTL may explain antixenosis to N. lugens. The N. lugens resistance<br />

genes bph11 and Bph13 map to chromosome 3 (Kawaguchi et al., 2001; Renganayaki et al.,<br />

2002). The N. lugens resistance genes Bph1, bph2, bph9, and Bph10 have been mapped to a<br />

25 cM block on rice chromosome 12 (Ishii et al., 1994; Hirabayashi and Ogawa, 1995; Murata<br />

et al., 2000; P.N. Sharma et al., 2003), while bph4 and bph12 map to chromosomes 6 and 4,<br />

respectively (Hirabayashi and Ogawa, 1999; Kawaguchi et al., 2001). A major resistance<br />

gene, Bph18(t), has been identifi ed in the introgression lines IR 65482-7-216-1-2, which had<br />

been derived from the wild rice, Oryza australiensis Domin. ( Jena et al., 2006). It is nonallelic<br />

to Bph10 and is located on the long arm terminal region of chromosome 12, fl anked by SSR<br />

marker RM463 and STS marker S15552.<br />

QTLs linked to green rice leafhopper, Nephotettix cincticeps (Uhler) resistance genes in<br />

rice have been identifi ed in progeny from doubled haploid populations involving indica<br />

and japonica rice crosses. Oryza sativa L. O. offi cinalis Wall ex Watt. crosses have also been<br />

used to identify QTLs for resistance to green leafhopper (N. Huang et al., 1997; Y. Fukuta<br />

et al., 1998; Z. Huang et al., 2001). Chromosomal location of the gene linked to early panicle<br />

initiation and resistance to green leafhopper resistance [Grh3(t)] have been used to identify

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