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Book of Abstracts <strong>First</strong> <strong>Legume</strong> <strong>Society</strong> <strong>Conference</strong> 2013: A <strong>Legume</strong> Odyssey Novi Sad, Serbia, 9-11 May 2013<br />
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Development of genomic resources for improvement of food legumes<br />
N Nadarajan 1 , Sanjeev Gupta 1 , Shiv Kumar 2 , Ashutosh Sarkar 3<br />
1 Indian Institute of Pulses Research, Kanpur, India<br />
2 International Center for Agricultural Research in the Dry Areas, Morocco<br />
3 International Center for Agricultural Research in the Dry Areas, New Delhi, India<br />
Among food legumes, chickpea, pigeon pea, lentil, peas, mungbean and common bean are<br />
assuming significance in terms of production at global level. Efforts have been made to develop<br />
genomic resources for improvement of these food legumes for their effective use in marker<br />
assisted breeding for important traits. Different types of molecular markers such as RFLPs,<br />
AFLPs, SSRs, CAPS, RGAs and ESTs have been developed for identification and mapping of<br />
genes and QTLs for many agriculturally important traits and occasionally for germplasm<br />
screening, fingerprinting, and marker-assisted breeding. A large number of microsatellites which<br />
are known to be abundant and uniformly distributed in the chickpea genome have been used to<br />
develop a genotyping kit, analyze genetic relationships among Cicer species and assess levels of<br />
cross-transferability. Further, these markers have also been applied for the construction of<br />
intraspecific and interspecific genetic linkage maps and for mapping genes of agronomic<br />
importance such as disease resistance and yield related traits, t<strong>here</strong>by demonstrating that SSRs are<br />
ideal tools for chickpea. Additionally, in chickpea only about 800 STMS markers have also been<br />
reported and only 30-40% is expected to be polymorphic. Similar has been the case for the ESTs,<br />
however, at present about 30,000 ESTs are available in public domain which can be used in<br />
chickpea improvement. The genome sequence of pigeon pea developed by two separate groups<br />
in recent has provided sufficient number of practical markers for improvement of this crop.<br />
Total 47,004 protein coding genes and 12,511 transposable elements related genes were<br />
postulated by one group while other group predicted 48,680 genes on 11 chromosomes of pigeon<br />
pea. At least 25 mapping populations of pigeon pea for a number of biotic and abiotic stresses<br />
are being currently developed. In terms of genomic resources, lentil is relatively under developed<br />
with limited available data. At present lentil specific 9,513 EST sequences are available in the<br />
public domain. T<strong>here</strong> is consequently a pressing need for significant efforts to either develop<br />
markers capable of cross-species transfer, in order to enrich existing genetic maps, or generate<br />
more informative species-specific genetic and genomic tools which can enable the identification<br />
of orthologous genes through genome synteny analysis in lentils. Comparatively, genomic<br />
resources for common bean are mostly available. Eleven BAC libraries and 83,000 ESTs and<br />
over 25 linkage maps, mostly low density (markers on average every 10 cM), have been developed<br />
for common bean. To maximize molecular polymorphism, the majority of mapping populations<br />
were derived from crosses between domesticated parents belonging to the Andean vs. Middle<br />
American gene pools. The development of genomic resources in Mungbean has been<br />
comparatively slow as only eight linkage maps are available and gene for bruchids tolerance and<br />
powdery mildew were mapped on chromosomes. Relatively very few markers are available in<br />
public domain, however, markers from other Vigna species like azukibean and blackgram showed<br />
polymorphism for Mungbean germplasm. This paper describes the current status of availability<br />
of genomic resources and focused the need of development of more practical markers for<br />
genomic enabled improvement in food legumes.<br />
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