Transferability of molecular markers from major legumes to Lathyrus spp. for their application in mapping and diversity studies

被引:24
|
作者
Almeida, Nuno Felipe [1 ]
Leitao, Susana Trindade [1 ]
Caminero, Constantino [2 ]
Maria Torres, Ana [3 ]
Rubiales, Diego [4 ]
Vaz Patto, Maria Carlota [1 ]
机构
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol, P-2780157 Oeiras, Portugal
[2] Consejeria Agr & Ganaderia, Inst Tecnol Agr, Valladolid 47071, Spain
[3] Ctr Alameda Obispo, IFAPA, Cordoba 14080, Spain
[4] CSIC, Inst Sustainable Agr, Cordoba 14080, Spain
关键词
Lathyrus spp; Microsatellite; Intron-targeted amplified polymorphic; Resistance gene analogue; Single nucleotide polymorphism; Cross-genera amplification; Legumes; EST-SSR MARKERS; CROSS-SPECIES AMPLIFICATION; MILDEW ERYSIPHE-PISI; MEDICAGO-TRUNCATULA; GENETIC DIVERSITY; SATIVUS L; MICROSATELLITE MARKERS; GERMPLASM COLLECTION; MYCOSPHAERELLA-PINODES; PHYLOGENETIC ANALYSIS;
D O I
10.1007/s11033-013-2860-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lathyrus cicera L. (chickling pea) and L. sativus L. (grass pea) have great potential among grain legumes due to their adaptability to inauspicious environments, high protein content and resistance to serious diseases. Nevertheless, due to its past underused, further activities are required to exploit this potential and to capitalise on the advances in molecular biology that enable improved Lathyrus spp. breeding programmes. In this study we evaluated the transferability of molecular markers developed for closely related legume species to Lathyrus spp. (Medicago truncatula, pea, lentil, faba bean and lupin) and tested the application of those new molecular tools on Lathyrus mapping and diversity studies. Genomic and expressed sequence tag microsatellite, intron-targeted amplified polymorphic, resistance gene analogue and defence-related gene markers were tested. In total 128 (27.7 %) and 132 (28.6 %) molecular markers were successfully cross-amplified, respectively in L. cicera and L. sativus. In total, the efficiency of transferability from genomic microsatellites was 5 %, and from gene-based markers, 55 %. For L. cicera, three cleaved amplified polymorphic sequence markers and one derived cleaved amplified polymorphic sequence marker based on the cross-amplified markers were also developed. Nine of those molecular markers were suitable for mapping in a L. cicera recombinant inbred line population. From the 17 molecular markers tested for diversity analysis, six (35 %) in L. cicera and seven (41 %) in L. sativus were polymorphic and discriminate well all the L. sativus accessions. Additionally, L. cicera accessions were clearly distinguished from L. sativus accessions. This work revealed a high number of transferable molecular markers to be used in current genomic studies in Lathyrus spp. Although their usefulness was higher on diversity studies, they represent the first steps for future comparative mapping involving these species.
引用
收藏
页码:269 / 283
页数:15
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