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SSR markers targeting (GATA) n motifs are known to be highly polymorphic and useful in many organisms. (GATA) n motif specific SSR markers covering the whole rice genome are not available. The present study was carried out with an objective to identify class I rice microsatellites in the rice genome with (GATA)n motifs, in-silico, and validate their potential as molecular markers. A total of 243 such motifs were identified; 65 of these were present in the genic region, 59 were in the upstream region and the remaining motifs were found in the intergenic regions. Many of the (GATA) n motifs were found within and/or upstream of genes associated with biotic or abiotic stress tolerance. A total of 230 PCR-based markers targeting all the class I (GATA) n microsatellites were developed and 35 of these markers spread across the rice genome were validated in a set of 24 representative rice varieties belonging to five distinct cultivar groups. All the markers were polymorphic, with average polymorphism information content (PIC) value of 0.61, and the rice cultivars could be uniquely distinguished into different cultivar groups based on marker analysis. These informative markers targeting (GATA) n motifs representing a new set of markers in rice will be highly useful for genetic studies and marker-assisted selection.Not Availabl

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Not AvailableThis study was undertaken to assess the comparative potential of 25 Expressed Sequence Tag derived simple sequence repeats (EST-SSRs) and 25 genomic SSRs in the prediction of grain yield heterosis using a set of nine cytoplasmic male sterile (CMS) lines and 32 restorer lines of rice. EST-SSRs and genomic SSRs exhibited an average Polymorphism Information Content value of 0.37 and 0.45, respectively. The coefficient of marker polymorphism among parental lines with respect to a set of hypervariable EST and genomic SSRs was correlated with standard heterosis for grain yield of six public bred rice hybrids. ESTSSRs gave a better correlation (r = 0.75) as compared with genomic SSRs (r = 0.09). When 10 key informative EST-SSR markers which showed a higher positive correlation with grain yield heterosis were validated in a new set of 14 experimental hybrids, the markers exhibited a higher correlation (r = 0.79), indicating the predictive value of these EST-SSRs. We recommend these 10 key informative EST-SSR markers for analysis of genetic diversity of parental lines and prediction of heterosis in hybrid rice breeding programmes.Not Availabl

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Not AvailableKMR-3R is a stable restorer line with medium-bold grain type and is the male parent of the popular public-bred Indian rice hybrid, KRH2. As both KMR-3R and KRH2 are highly susceptible to bacterial blight (BB) and possess undesirable bold-grain type, we crossed KMR-3R with a high-yielding, BB resistant, fine-grain-type variety, Improved Samba Mahsuri, possessing the major BB resistant gene, Xa21. The F1s were backcrossed to KMR-3R, and the BC1F1 plants were subjected to marker-assisted selection (MAS) for Xa21 and two major fertility restorer genes, Rf3 and Rf4. Triple positive BC1F1 plants were selfed and their progeny were subjected to MAS for Xa21 coupled with phenotype-based visual selection for agromorphological and grainquality traits. At BC1F5 generation, three backcross derived lines (BK9, BK49 and BK61) possessing higher yield than KMR-3R, tall plant stature along with fine-grain type were identified and crossed with IR598025A, the female parent of KRH2. The hybrids were completely fertile, possessed long-slender grain type, exhibited resistance to BB and displayed a yield advantage of 24% over KRH2 under BB infectionIndian Council of Agricultural Research (ICAR) and Department of Biotechnology (DBT

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Not AvailableThe cultivar Ajaya (IET 8585) exhibits durable broad-spectrum resistance to bacterial blight (BB) disease of rice and is widely used as a resistance donor. The present study was carried out to decipher the genetics of BB resistance in Ajaya and map the gene(s) conferring resistance. Genetic analysis in the F2 indicated a quantitative/additive nature of resistance governed by two loci with equal effects. Linked marker analysis and allelic tests revealed that one of the resistance genes is xa5. Sequence analysis of a 244 bp region of the second exon of the gene-encoding Transcription factor IIAγ (the candidate gene for xa5) confirmed the presence of xa5. Bulked-segregant analysis (BSA) revealed the putative location of the two quantitative trait loci (QTLs)/genes associated with resistance on chromosomes 5 and 8. Composite interval mapping located the first locus on Chr. 5S exactly in the genomic region spanned by xa5 and the second locus (qtl BBR 8.1) on Chr. 8L. Owing to its differential disease reaction with a set of seven hyper-virulent isolates of Xanthomonas oryzae, a map location on Chr. 8L, which was distinct from xa13 and data from allelism tests, the second resistance locus in Ajaya was determined to be novel and was designated as xaAj. A contig map spanning xaAj was constructed in silico and the genomic region was delimited to a 13·5 kb physical interval. In silico analysis of the genomic region spanning xaAj identified four putatively expressed candidate genes, one of which could be involved in imparting BB resistance in Ajaya along with xa5.Council for Scientific and Industrial Research (CSIR), Government of IndiaDepartment of Biotechnology, Government of IndiaIndian Council for Agricultural Research, Government of Indi

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Not AvailableIR 58025A is a very popular wild-abortive cytoplasmic male sterile (WA-CMS) line of rice and is extensively used for hybrid rice breeding. However, IR 58025A and many hybrids derived from it possess mild aroma (undesirable in some parts of India) and are highly susceptible to bacterial blight (BB) and blast diseases. To improve IR 58025A for BB and blast resistance, we have introgressed a major dominant gene conferring resistance against BB (i.e. Xa21) and blast (i.e. Pi54) into IR 58025B, the maintainer line of IR 58025A. An introgression line of Samba Mahsuri (i.e. SM2154) possessing Xa21 and Pi54 genes in homozygous condition and fine-grain type was used as donor parent, and backcross breeding strategy was adopted for targeted introgression of the resistance genes. PCR-based molecular markers tightly linked to Xa21 and Pi54 were used for selection of BB- and blast-resistant lines, while closely linked markers were used for identification of backcross-derived plants devoid of Rf4 and aroma. At BC2F5, four backcross-derived lines possessing resistance against BB and blast, devoid of aroma, high yield, short plant stature, long-slender grain type and with recurrent parent genome recovery ranging from 88.8% to 98.6% were selected and advanced for further evaluation. The improved versions of IR 58025B, viz. SB54-11-143-9-44-5, SB54-11-143-9-44-98, SB54-11-143-9-44-111 and SB54-11-143-9-44-171, behaved as perfect maintainers when test-crossed with WA-CMS lines. Agronomically superior lines of improved IR 58025B are being converted to CMS line through backcrossing for developing high-yielding and biotic stress-resistant rice hybrids.Not Availabl

BB & BL resistance into IR58025B

Not AvailableIR 58025A is a very popular wild-abortive cytoplasmic male sterile (WA-CMS) line of rice and is extensively used for hybrid rice breeding. However, IR 58025A and many hybrids derived from it possess mild aroma (undesirable in some parts of India) and are highly susceptible to bacterial blight (BB) and blast diseases. To improve IR 58025A for BB and blast resistance, we have introgressed a major dominant gene confer- ring resistance against BB (i.e. Xa21) and blast (i.e. Pi54) into IR 58025B, the maintainer line of IR 58025A. An introgression line of Samba Mahsuri (i.e. SM2154) possessing Xa21 and Pi54 genes in homo- zygous condition and fine-grain type was used as donor parent, and backcross breeding strategy was adopted for targeted introgression of the resistance genes. PCR-based molecular markers tightly linked to Xa21 and Pi54 were used for selection of BB- and blast-resistant lines, while closely linked markers were used for identification of backcross-derived plants devoid of Rf4 and aroma. At BC2F5, four backcross-derived lines possessing resistance against BB and blast, devoid of aroma, high yield, short plant stature, long-slender grain type and with recurrent parent genome recovery ranging from 88.8% to 98.6% were selected and advanced for further evaluation. The improved versions of IR 58025B, viz. SB54-11-143-9-44-5, SB54-11-143-9-44-98, SB54-11-143-9-44-111 and SB54-11-143-9-44-171, behaved as perfect maintainers when test- crossed with WA-CMS lines. Agronomically superior lines of improved IR 58025B are being converted to CMS line through backcrossing for developing high-yielding and biotic stress-resistant rice hybrids.Not Availabl

Recent advances in rapid and sensitive screening for abiotic stress tolerance

Traditionally, screening for abiotic stress tolerance at field level was based on necrosis scores and shoot biomass reduction on stress exposure, relative to unstressed controls. However, such a measure of tolerance screening is laborious, destructive, and time consuming, and results are subjected to environmental variation. Recently, noninvasive, high-throughput screening techniques have been developed for screening abiotic stress tolerance in crops. In this direction, some physiological, biochemical, and/or molecular indicators/markers have been identified for rapid and sensitive indirect screening of germplasm. Physiological markers like membrane damage based on electrolyte leakage, stomatal conductance, chlorophyll content and so on are currently available. In addition, quick and sensitive screening in crop plants is possible with biochemical markers like status of reactive oxygen species and oxidative damage to biological macromolecules like lipids, proteins, and nucleic acids. Identification of molecular markers associated with the tolerance response has also made rapid and sensitive indirect selection possible in a few crop species. Thus, development of such methods is valuable in breeding for abiotic stress tolerance in plants