Varshney, R K and Penmetsa, R V and Dutta, S and Kulwal, P L and Saxena, R K and Datta, S and Sharma, T R and Rosen, B and Carrasquilla-Garcia, N and Farmer, A D and Dubey, A and Saxena, K B and Gao, J and Fakrudin, B and Singh, M N and Singh, B P and Wanjari, K B and Yuan, M and Srivastava, R K and Kilian, A and Upadhyaya, H D and Mallikarjuna, N and Town, C D and Bruening, G E and He, G and May, G D and McCombie, R and Jackson, S A and Singh, N K and Cook, D R (2010) Pigeonpea genomics initiative (PGI): an international effort to improve crop productivity of pigeonpea (Cajanus cajan L.). Molecular Breeding, 26 (3). pp. 393-408. ISSN 1380-3743
|
PDF (Author pay open access)
Download (2MB) | Preview |
Abstract
Pigeonpea (Cajanus cajan), an important food legume crop in the semi-arid regions of the world and the second most important pulse crop in India, has an average crop productivity of 780 kg/ha. The relatively low crop yields may be attributed to non-availability of improved cultivars, poor crop husbandry and exposure to a number of biotic and abiotic stresses in pigeonpea growing regions. Narrow genetic diversity in cultivated germplasm has further hampered the effective utilization of conventional breeding as well as development and utilization of genomic tools, resulting in pigeonpea being often referred to as an 'orphan crop legume'. To enable genomics-assisted breeding in this crop, the pigeonpea genomics initiative (PGI) was initiated in late 2006 with funding from Indian Council of Agricultural Research under the umbrella of Indo-US agricultural knowledge initiative, which was further expanded with financial support from the US National Science Foundation's Plant Genome Research Program and the Generation Challenge Program. As a result of the PGI, the last 3 years have witnessed significant progress in development of both genetic as well as genomic resources in this crop through effective collaborations and coordination of genomics activities across several institutes and countries. For instance, 25 mapping populations segregating for a number of biotic and abiotic stresses have been developed or are under development. An 11X-genome coverage bacterial artificial chromosome (BAC) library comprising of 69,120 clones have been developed of which 50,000 clones were end sequenced to generate 87,590 BAC-end sequences (BESs). About 10,000 expressed sequence tags (ESTs) from Sanger sequencing and ca. 2 million short ESTs by 454/FLX sequencing have been generated. A variety of molecular markers have been developed from BESs, microsatellite or simple sequence repeat (SSR)-enriched libraries and mining of ESTs and genomic amplicon sequencing. Of about 21,000 SSRs identified, 6,698 SSRs are under analysis along with 670 orthologous genes using a GoldenGate SNP (single nucleotide polymorphism) genotyping platform, with large scale SNP discovery using Solexa, a next generation sequencing technology, is in progress. Similarly a diversity array technology array comprising of ca. 15,000 features has been developed. In addition, > 600 unique nucleotide binding site (NBS) domain containing members of the NBS-leucine rich repeat disease resistance homologs were cloned in pigeonpea; 960 BACs containing these sequences were identified by filter hybridization, BES physical maps developed using high information content fingerprinting. To enrich the genomic resources further, sequenced soybean genome is being analyzed to establish the anchor points between pigeonpea and soybean genomes. In addition, Solexa sequencing is being used to explore the feasibility of generating whole genome sequence. In summary, the collaborative efforts of several research groups under the umbrella of PGI are making significant progress in improving molecular tools in pigeonpea and should significantly benefit pigeonpea genetics and breeding. As these efforts come to fruition, and expanded (depending on funding), pigeonpea would move from an 'orphan legume crop' to one where genomics-assisted breeding approaches for a sustainable crop improvement are routine.
Item Type: | Article |
---|---|
Divisions: | UNSPECIFIED |
CRP: | UNSPECIFIED |
Uncontrolled Keywords: | Molecular markers; Genetic mapping; Trait mapping;Genomics;Next generation;sequencing; Gene discovery;Crop improvement |
Agro Tags: | <b>Agrotags</b> - chickpeas | genetics | genomes | dna | genes | polymorphism | apples | genotypes | containers | locus <br><b>Fishtags</b> - roes <br><b>Geopoliticaltags</b> - india | turkey | usa | germany | andhra pradesh | syria | afghanistan | nepal | pakistan | maine |
Subjects: | Mandate crops > Pigeonpea |
Depositing User: | Siva Shankar |
Date Deposited: | 09 Jun 2011 06:24 |
Last Modified: | 01 Sep 2011 12:47 |
URI: | http://oar.icrisat.org/id/eprint/72 |
Official URL: | http://dx.doi.org/10.1007/s11032-009-9327-2 |
Projects: | UNSPECIFIED |
Funders: | Indian Council of Agricultural Research, Generation Challenge Programme, National Science Foundation (NSF), USA |
Acknowledgement: | Authors are thankful to several research scholars and post-doctoral fellows working in the laboratories of collaborating research institutes of PGI as well as a number of collaborators engaged directly or indirectly in research activities of PGI. Authors would like to extend their sincere thanks to Dr. Mangla Rai, Director General, Indian Council of Agricultural Research (ICAR) and Secretary, Department of Agricultural Research and Extension (DARE) for his support in initiating the PGI under the Indo-US Agricultural Knowledge Initiative (AKI). Thanks are also due to Dr. Satya Prakash Tiwari, Deputy Director General (Education), ICAR; Dr. Jean- Marcel Ribaut, Director, Generation Challenge Programme (GCP, www.generationcp.org); Dr. William Dar, Director General, ICRISAT and Dr. Dave Hoisington, Deputy Director General-Research, ICRISAT for their strong support for pigeonpea genomics activities. Research in the laboratories of authors presented in this article is supported by ICAR under the umbrella of Indo-US AKI, Generation Challenge Program (GCP), and the National Science Foundation (USA). |
Links: |
Actions (login required)
View Item |