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
NCPGR100NCPGR100genetic_marker
NCPGR21NCPGR21genetic_marker
NCPGR23NCPGR23genetic_marker
NCPGR27NCPGR27genetic_marker
NCPGR28NCPGR28genetic_marker
NCPGR29NCPGR29genetic_marker
NCPGR30NCPGR30genetic_marker
NCPGR32NCPGR32genetic_marker
NCPGR33NCPGR33genetic_marker
NCPGR34NCPGR34genetic_marker
NCPGR36NCPGR36genetic_marker
NCPGR37NCPGR37genetic_marker
NCPGR38NCPGR38genetic_marker
NCPGR39NCPGR39genetic_marker
NCPGR40NCPGR40genetic_marker
NCPGR41NCPGR41genetic_marker
NCPGR42NCPGR42genetic_marker
NCPGR43NCPGR43genetic_marker
NCPGR44NCPGR44genetic_marker
NCPGR45NCPGR45genetic_marker
NCPGR46NCPGR46genetic_marker
NCPGR47NCPGR47genetic_marker
NCPGR48NCPGR48genetic_marker
NCPGR49NCPGR49genetic_marker
NCPGR50NCPGR50genetic_marker

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