Development of microsatellite markers and analysis of intraspecific genetic variability in chickpea (Cicer arietinum L.)

Publication Overview
TitleDevelopment of microsatellite markers and analysis of intraspecific genetic variability in chickpea (Cicer arietinum L.)
AuthorsSethy NK, Shokeen B, Edwards KJ, Bhatia S
TypeJournal Article
Journal NameTheor Appl Genet
Volume112
Year2006
Page(s)1416-1428
CitationSethy NK, Shokeen B, Edwards KJ, Bhatia S. Development of microsatellite markers and analysis of intraspecific genetic variability in chickpea (Cicer arietinum L.). Theor Appl Genet. 2006; 112:1416-1428.

Abstract

Paucity of polymorphic molecular markers in chickpea (Cicer arietinum L.) has been a major limitation in the improvement of this important legume. Hence, in an attempt to develop sequence-tagged microsatellite sites (STMS) markers from chickpea, a microsatellite enriched library from the C. arietinum cv. Pusa362 nuclear genome was constructed for the identification of (CA/GT)n and (CT/GA)n microsatellite motifs. A total of 92 new microsatellites were identified, of which 74 functional STMS primer pairs were developed. These markers were validated using 9 chickpea and one C. reticulatum accession. Of the STMS markers developed, 25 polymorphic markers were used to analyze the intraspecific genetic diversity within 36 geographically diverse chickpea accessions. The 25 primer pairs amplified single loci producing a minimum of 2 and maximum of 11 alleles. A total of 159 alleles were detected with an average of 6.4 alleles per locus. The observed and expected heterozygosity values averaged 0.32 (0.08-0.91) and 0.74 (0.23-0.89) respectively. The UPGMA based dendrogram was able to distinguish all the accessions except two accessions from Afghanistan establishing that microsatellites could successfully detect intraspecific genetic diversity in chickpea. Further, cloning and sequencing of size variant alleles at two microsatellite loci revealed that the variable numbers of AG repeats in different alleles were the major source of polymorphism. Point mutations were found to occur both within and immediately upstream of the long tracts of perfect repeats, thereby bringing about a conversion of perfect motifs into imperfect or compound motifs. Such events possibly occurred in order to limit the expansion of microsatellites and also lead to the birth of new microsatellites. The microsatellite markers developed in this study will be useful for genetic diversity analysis, linkage map construction as well as for depicting intraspecific microsatellite evolution.
Features
This publication contains information about 74 features:
Feature NameUniquenameType
NCPGR51NCPGR51genetic_marker
NCPGR52NCPGR52genetic_marker
NCPGR53NCPGR53genetic_marker
NCPGR54NCPGR54genetic_marker
NCPGR55NCPGR55genetic_marker
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NCPGR57NCPGR57genetic_marker
NCPGR58NCPGR58genetic_marker
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NCPGR64NCPGR64genetic_marker
NCPGR65NCPGR65genetic_marker
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NCPGR67NCPGR67genetic_marker
NCPGR68NCPGR68genetic_marker
NCPGR69NCPGR69genetic_marker
NCPGR70NCPGR70genetic_marker
NCPGR71NCPGR71genetic_marker
NCPGR72NCPGR72genetic_marker
NCPGR73NCPGR73genetic_marker
NCPGR74NCPGR74genetic_marker
NCPGR75NCPGR75genetic_marker

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URLhttp://link.springer.com/article/10.1007%2Fs00122-006-0243-0