Mapping QTL tolerance to Phytophthora root rot in soybean using microsatellite and RAPD/SCAR derived markers

被引:72
|
作者
Han, Yingpeng [1 ]
Teng, Weili [1 ]
Yu, Kangfu [2 ]
Poysa, Vaino [2 ]
Anderson, Terry [2 ]
Qiu, Lijuan [3 ]
Lightfoot, David A. [4 ]
Li, Wenbin [1 ]
机构
[1] NE Agr Univ, Biol Chinese Educ Minist, Soybean Res Inst, Key Lab Soybean, Harbin 150030, Peoples R China
[2] Agr & Agri Food Canada, Green & Processing Crops Res Ctr, Harrow, ON N0R 1G0, Canada
[3] Chinese Acad Sci, Inst Crop Sci, Beijing 100081, Peoples R China
[4] So Illinois Univ, Ctr Excellence Soybean Res, Carbondale, IL 62901 USA
基金
美国国家科学基金会;
关键词
quantitative trait loci; SSR marker; SCAR marker; marker-assistant selection; phytophthora root rot; soybean;
D O I
10.1007/s10681-007-9558-4
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Broad tolerance to phytophthora root rot (PRR) caused by Phytophthora sojae has become an important goal for the improvement of soybean (Glycine max) because of the rapid spread of races that defeat the available resistance genes. The aim of this research was to identify the location of quantitative trait loci (QTL) in 'Conrad', a soybean cultivar with broad tolerance to many races of P. sojae. A PRR susceptible breeding line 'OX760-6-1' was crossed with Conrad. Through single-seed-descent, 112, F-2 derived, F-7 recombinant inbred lines (RILs) were advanced. A total of 39 random amplified polymorphic DNA bands (RAPDs) and 89 type 1 microsatellite (simple sequence repeat; SSR) markers were used to construct a genetic linkage map. In the greenhouse, RILs were inoculated with four P. sojae isolates (three from China and one from Canada). Disease was measured as the percent of dead plants 20 days after germination in P. sojae inoculated vermiculite in the greenhouse. Three QTLs (QGP1, QGP2, QGP3) for PRR tolerance in the greenhouse were detected using WinQTLCart 2.0 with a log-likelihood (LOD) score 27.14 acquired through permutations (1,000 at P <= 0.05). QGP1 (near Satt509) was located at linkage group F and explained 13.2%, 5.9%, and 6.7% of the phenotypic variance for tolerance to the JiXi, JianSanJiang and ShuangYaShan isolates, respectively. QGP2 (near Satt334) was located in a different interval on linkage group F and explained 5.1% and 2.4% of the phenotypic variance for JiXi and ShuangYaShan isolates, respectively. QGP3 was located on linkage group D1b + W (near OPL18(800)/SCL18(659)) and explained 10.2% of the phenotypic variance for Woodslee isolate. QGP1 and QGP2 appeared to be associated with PRR tolerance across a range of isolates but QGP3 was active only against the Woodslee isolate. At Woodslee and Weaver (in Ontario) in 2000, the interval associated with QGP3 explained 21.6% and 16.7% of phenotypic variance in resistance to PRR, respectively and was referred as QFP1. The identified QTLs would be beneficial for marker assistant selection of PRR tolerance varieties against both China and North America P. sojae races.
引用
收藏
页码:231 / 239
页数:9
相关论文
共 50 条
  • [31] Enhanced tolerance to Phytophthora root and stem rot by over-expression of the plant antimicrobial peptide CaAMP1 gene in soybean
    Lu Niu
    Xiaofang Zhong
    Yuanyu Zhang
    Jing Yang
    Guojie Xing
    Haiyun Li
    Dongbo Liu
    Rui Ma
    Yingshan Dong
    Xiangdong Yang
    BMC Genetics, 21
  • [32] Mapping of partial resistance to Phytophthora sojae in soybean PIs using whole-genome sequencing reveals a major QTL
    de Ronne, Maxime
    Santhanam, Parthasarathy
    Cinget, Benjamin
    Labbe, Caroline
    Lebreton, Amandine
    Ye, Heng
    Vuong, Tri D.
    Hu, Haifei
    Valliyodan, Babu
    Edwards, David
    Nguyen, Henry T.
    Belzile, Francois
    Belanger, Richard
    PLANT GENOME, 2022, 15 (01):
  • [33] Mapping QTL associated with partial resistance to Aphanomyces root rot in pea (Pisum sativum L.) using a 13.2 K SNP array and SSR markers
    Longfei Wu
    Rudolph Fredua-Agyeman
    Sheau-Fang Hwang
    Kan-Fa Chang
    Robert L. Conner
    Debra L. McLaren
    Stephen E. Strelkov
    Theoretical and Applied Genetics, 2021, 134 : 2965 - 2990
  • [34] Mapping QTL associated with partial resistance to Aphanomyces root rot in pea (Pisum sativum L.) using a 13.2 K SNP array and SSR markers
    Wu, Longfei
    Fredua-Agyeman, Rudolph
    Hwang, Sheau-Fang
    Chang, Kan-Fa
    Conner, Robert L.
    McLaren, Debra L.
    Strelkov, Stephen E.
    THEORETICAL AND APPLIED GENETICS, 2021, 134 (09) : 2965 - 2990
  • [35] Mapping the QTL and tagging yield traits in bitter gourd (Momordica charantia L.) using microsatellite markers
    Lavale, Shivaji Ajinath
    Mathew, Deepu
    Pradeepkumar, T.
    John, K. Joseph
    Joseph, Jiji
    BIOCATALYSIS AND AGRICULTURAL BIOTECHNOLOGY, 2023, 47
  • [36] IDENTIFICATION AND MAPPING OF GROWTH-RELATED QTL USING MICROSATELLITE AND AFLP MARKERS FOR THE PACIFIC OYSTER, CRASSOSTREA GIGAS
    Stick, David A.
    Camara, Mark D.
    JOURNAL OF SHELLFISH RESEARCH, 2012, 31 (01): : 349 - 349
  • [37] FINE MAPPING OF MILK YIELD QTL ON CHROMOSOMES 6 AND 20 IN GERMAN HOLSTEIN POPULATION USING MICROSATELLITE MARKERS
    Peter, Reinecke
    Monika, Reissmann
    Uwe, Mueller
    Salah, Abdel-Rahman
    JOURNAL OF CENTRAL EUROPEAN AGRICULTURE, 2005, 6 (04): : 501 - 507
  • [38] Genetic Variability and Relationships among Seventeen Trichoderma Isolates to Control Dry Root Rot Disease Using RAPD Markers
    Gopal, Kuruba
    Sreenivasulu, Yasodam
    Gopi, Venati
    Prasadbabu, Gundala
    Kumar, Teruvai Bharat
    Madhusudhan, Puchakayala
    Ahemed, Shaik Khayum
    Palanivel, Sellappa Gounder
    ZEITSCHRIFT FUR NATURFORSCHUNG SECTION C-A JOURNAL OF BIOSCIENCES, 2008, 63 (9-10): : 740 - 746
  • [39] Differentiation of isolates of cotton root rot pathogens Rhizioctonia solani and R-bataticola using pathogenicity and RAPD markers
    Monga, D
    Rathore, SS
    Mayee, CD
    Sharma, TR
    JOURNAL OF PLANT BIOCHEMISTRY AND BIOTECHNOLOGY, 2004, 13 (02) : 135 - 139
  • [40] Differentiation of Isolates of Cotton Root Rot Pathogens Rhizoctonia solani and R. bataticola Using Pathogenicity and RAPD Markers
    D. Monga
    S. S. Rathore
    C. D. Mayee
    T. R. Sharma
    Journal of Plant Biochemistry and Biotechnology, 2004, 13 : 135 - 139