Integration of novel SSR and gene-based SNP marker loci in the chickpea genetic map and establishment of new anchor points with Medicago truncatula genome

被引:172
|
作者
Nayak, Spurthi N. [1 ,2 ]
Zhu, Hongyan [3 ,4 ]
Varghese, Nicy [1 ]
Datta, Subhojit [3 ,5 ]
Choi, Hong-Kyu [3 ,6 ]
Horres, Ralf [7 ]
Juengling, Ruth [7 ]
Singh, Jagbir [1 ,8 ]
Kishor, P. B. Kavi [2 ]
Sivaramakrishnan, S. [8 ]
Hoisington, Dave A. [1 ]
Kahl, Guenter [7 ,9 ]
Winter, Peter [9 ]
Cook, Douglas R. [3 ]
Varshney, Rajeev K. [1 ,10 ]
机构
[1] Int Crops Res Inst Semi Arid Trop, Ctr Excellence Genom, Patancheru 502324, Andhra Pradesh, India
[2] Osmania Univ, Dept Genet, Hyderabad 500007, Andhra Pradesh, India
[3] Univ Calif Davis, Dept Plant Pathol, Davis, CA 95616 USA
[4] Univ Kentucky, Dept Plant & Soil Sci, Lexington, KY 40546 USA
[5] Indian Inst Pulses Res, Kanpur 208024, Uttar Pradesh, India
[6] Dong A Univ, Dept Genet Engn, Pusan 604714, South Korea
[7] Goethe Univ Frankfurt, D-60439 Frankfurt, Germany
[8] Acharya NG Ranga Agr Univ, Dept Agr Biotechnol, Hyderabad 500030, Andhra Pradesh, India
[9] GenXPro GmbH, Frankfurter Innovat Zentrum Biotechnol FIZ, D-60438 Frankfurt, Germany
[10] CIMMYT, GCP, Genom Gene Discovery Subprogramme, Mexico City 06600, DF, Mexico
基金
美国国家科学基金会;
关键词
TAGGED MICROSATELLITE SITES; RESISTANCE GENE; DISEASE RESISTANCE; CICER-RETICULATUM; FUSARIUM-WILT; L; IDENTIFICATION; EVOLUTION; FREQUENCY; LINKAGE;
D O I
10.1007/s00122-010-1265-1
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
This study presents the development and mapping of simple sequence repeat (SSR) and single nucleotide polymorphism (SNP) markers in chickpea. The mapping population is based on an inter-specific cross between domesticated and non-domesticated genotypes of chickpea (Cicer arietinum ICC 4958 x C. reticulatum PI 489777). This same population has been the focus of previous studies, permitting integration of new and legacy genetic markers into a single genetic map. We report a set of 311 novel SSR markers (designated ICCM-ICRISAT chickpea microsatellite), obtained from an SSR-enriched genomic library of ICC 4958. Screening of these SSR markers on a diverse panel of 48 chickpea accessions provided 147 polymorphic markers with 2-21 alleles and polymorphic information content value 0.04-0.92. Fifty-two of these markers were polymorphic between parental genotypes of the inter-specific population. We also analyzed 233 previously published (H-series) SSR markers that provided another set of 52 polymorphic markers. An additional 71 gene-based SNP markers were developed from transcript sequences that are highly conserved between chickpea and its near relative Medicago truncatula. By using these three approaches, 175 new marker loci along with 407 previously reported marker loci were integrated to yield an improved genetic map of chickpea. The integrated map contains 521 loci organized into eight linkage groups that span 2,602 cM, with an average inter-marker distance of 4.99 cM. Gene-based markers provide anchor points for comparing the genomes of Medicago and chickpea, and reveal extended synteny between these two species. The combined set of genetic markers and their integration into an improved genetic map should facilitate chickpea genetics and breeding, as well as translational studies between chickpea and Medicago.
引用
收藏
页码:1415 / 1441
页数:27
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