Simple sequence repeat (SSR) markers survey of the cassava (Manihot esculenta Crantz) genome: towards an SSR-based molecular genetic map of cassava |
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| Authors: | R. E. C. Mba P. Stephenson K. Edwards S. Melzer J. Nkumbira U. Gullberg K. Apel M. Gale J. Tohme M. Fregene |
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| Affiliation: | (1) Biotechnology Research Unit, International Center for Tropical Agriculture (CIAT), AA6713 Cali, Colombia and National Root Crops Research Institute, Umudike, Abia State, Nigeria e-mail: C.Mba@cgiar.org, NG;(2) John Innes Center for Plant Sciences, Norwich Research Park, Coloney, Norwich NR4 7UJ, UK, GB;(3) IARC-Long Ashton Research Station, Department of Agricultural Sciences, University of Bristol, Long Ashton, Bristol BS18 9AF, UK, GB;(4) Institute for Plant Sciences, Swiss Institute of Technology, Zurich, Switzerland, CH;(5) Department of Plant Biolology, Swedish Agricultural University (SLU), Uppsala, Sweden, SE;(6) Biotechnology, Research Unit, International Center for Tropical Agriculture, Cali, Colombia, CO |
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| Abstract: | The development of PCR-based, easily automated molecular genetic markers, such as SSR markers, are required for realistic cost-effective marker-assisted selection schemes. This paper describes the development and characterization of 172 new SSR markers for the cassava genome. The placement of 36 of these markers on the existing RFLP framework map of cassava is also reported. Two similar enrichment methods were employed. The first method yielded 35 SSR loci, for which primers could be designed, out of 148 putative DNA clones. A total of 137 primer pairs could be designed from 544 putative clones sequenced for the second enrichment. Most of the SSRs (95%) were di-nucleotide repeats, and 21% were compound repeats. A major drawback of these methods of SSR discovery is the redundancy – 20% duplication; in addition, primers could not be designed for many SSR loci that were too close to the cloning site – 45% of the total. All 172 SSRs amplified the corresponding loci in the parents of the mapping progeny, with 66% of them revealing a unique allele in at least one of the parents, and 26% having unique alleles in both of the parents. Of the 36 SSRs that have been mapped, at least 1 was placed on 16 out of the 18 linkage groups of the framework map, indicating a broad coverage of the cassava genome. This preliminary mapping of the 36 markers has led to the joining of a few small groups and the creation of one new group. The abundance of allelic bridges as shown by these markers will lead to the development of a consensus map of the male- and female-derived linkage groups. In addition, the relatively higher number of these allelic bridges, 30% as against 10% for RFLPs in cassava, underscores SSR as the marker of choice for cassava. The 100% primer amplification obtained for this set of primers also confirms the appropriateness of SSR markers for use in cassava genome analysis and the transferability of the technology as a low-cost approach to increasing the efficiency of cassava breeding. Current efforts are geared towards the generation of more SSR markers to attain a goal of 200 SSR markers, or 1 SSR marker every 10 cM. Received: 15 November 1999 / Accepted: 14 April 2000 |
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| Keywords: | Cassava Molecular genetic markers Simple sequence repeats Enriched libraries Molecular genetic map |
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