A High-Density Integrated DArTseq SNP-Based Genetic Map of Pisum fulvum and Identification of QTLs Controlling Rust Resistance

被引:53
作者
Barilli, Eleonora [1 ]
Cobos, Maria J. [1 ]
Carrillo, Estefania [1 ]
Kilian, Andrzej [2 ]
Carling, Jason [2 ]
Rubiales, Diego [1 ]
机构
[1] CSIC, Inst Sustainable Agr, Cordoba, Spain
[2] Univ Canberra, Divers Arrays Technol Pty Ltd, Canberra, ACT, Australia
来源
FRONTIERS IN PLANT SCIENCE | 2018年 / 9卷
关键词
DArT; Pisum fulvum; genetic linkage map; QTL; rust resistance; Uromyces pisi; QUANTITATIVE TRAIT LOCI; UROMYCES-FABAE RESISTANCE; OROBANCHE-CRENATA FORSK; SATIVUM L; LINKAGE MAP; GENOMIC REGIONS; CANDIDATE GENES; POWDERY MILDEW; PEA; MARKERS;
D O I
10.3389/fpls.2018.00167
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Pisum fulvum, a wild relative of pea is an important source of allelic diversity to improve the genetic resistance of cultivated species against fungal diseases of economic importance like the pea rust caused by Uromyces pisi. To unravel the genetic control underlying resistance to this fungal disease, a recombinant inbred line (RIL) population was generated from a cross between two P. fulvum accessions, IFPI3260 and IFPI3251, and genotyped using Diversity Arrays Technology. A total of 9,569 high-quality DArT-Seq and 8,514 SNPs markers were generated. Finally, a total of 12,058 markers were assembled into seven linkage groups, equivalent to the number of haploid chromosomes of P. fulvum and P. sativum. The newly constructed integrated genetic linkage map of P. fulvum covered an accumulated distance of 1,877.45 cM, an average density of 1.19 markers cM(-1) and an average distance between adjacent markers of 1.85 cM. The composite interval mapping revealed three QTLs distributed over two linkage groups that were associated with the percentage of rust disease severity (DS%). QTLs UpDSII and UpDSIV were located in the LGs II and IV respectively and were consistently identified both in adult plants over 3 years at the field (Cordoba, Spain) and in seedling plants under controlled conditions. Whenever they were detected, their contribution to the total phenotypic variance varied between 19.8 and 29.2. A third QTL (UpDSIV. 2) was also located in the LGIVand was environmentally specific as was only detected for DS % in seedlings under controlled conditions. It accounted more than 14% of the phenotypic variation studied. Taking together the data obtained in the study, it could be concluded that the expression of resistance to fungal diseases in P. fulvum originates from the resistant parent IFPI3260.
引用
收藏
页数:13
相关论文
共 59 条
  • [11] Identification of quantitative trait loci and candidate genes for specific cellular resistance responses against Didymella pinodes in pea
    Carrillo, E.
    Satovic, Z.
    Aubert, G.
    Boucherot, K.
    Rubiales, D.
    Fondevilla, S.
    [J]. PLANT CELL REPORTS, 2014, 33 (07) : 1133 - 1145
  • [12] Identification and characterization of slow rusting components in pea (Pisum sativum L.)
    Chand, R
    Srivastava, CP
    Singh, BD
    Sarode, SB
    [J]. GENETIC RESOURCES AND CROP EVOLUTION, 2006, 53 (02) : 219 - 224
  • [13] A linkage map of chickpea (Cicer arietinum L.) based on populations from Kabuli x Desi crosses:: location of genes for resistance to fusarium wilt race 0
    Cobos, MJ
    Fernández, M
    Rubio, J
    Kharrat, M
    Moreno, MT
    Gil, J
    Millán, T
    [J]. THEORETICAL AND APPLIED GENETICS, 2005, 110 (07) : 1347 - 1353
  • [14] Identification of QTL controlling high levels of partial resistance to Fusarium solani f. sp pisi in pea
    Coyne, Clarice J.
    Pilet-Nayel, Marie-Laure
    McGee, Rebecca J.
    Porter, Lyndon D.
    Smykal, Petr
    Gruenwald, Niklaus J.
    [J]. PLANT BREEDING, 2015, 134 (04) : 446 - 453
  • [15] Distorted segregation resulting from pea chromosome reconstructions with alien segments from Pisum fulvum
    De Martino, T
    Errico, A
    Lassandro, A
    Conicella, C
    [J]. JOURNAL OF HEREDITY, 2000, 91 (04) : 322 - 325
  • [16] Highly-multiplexed SNP genotyping for genetic mapping and germplasm diversity studies in pea
    Deulvot, Chrystel
    Charrel, Helene
    Marty, Amandine
    Jacquin, Francoise
    Donnadieu, Cecile
    Lejeune-Henaut, Isabelle
    Burstin, Judith
    Aubert, Gregoire
    [J]. BMC GENOMICS, 2010, 11
  • [17] DOYLE J. J., 1987, PHYTOCHEMISTRY B, V19, P1
  • [18] An integrated and comparative view of pea genetic and cytogenetic maps
    Ellis, THN
    Poyser, SJ
    [J]. NEW PHYTOLOGIST, 2002, 153 (01) : 17 - 25
  • [19] Development of DArT-based PCR markers for selecting drought-tolerant spring barley
    Fiust, Anna
    Rapacz, Marcin
    Wojcik-Jagla, Magdalena
    Tyrka, Miroslaw
    [J]. JOURNAL OF APPLIED GENETICS, 2015, 56 (03) : 299 - 309
  • [20] Mapping of quantitative trait loci for resistance to Mycosphaerella pinodes in Pisum sativum subsp syriacum
    Fondevilla, S.
    Satovic, Z.
    Rubiales, D.
    Moreno, M. T.
    Torres, A. M.
    [J]. MOLECULAR BREEDING, 2008, 21 (04) : 439 - 454