MSU Dry Bean Breeding and Genetics Program
PROGRAM OBJECTIVES

The Role of RAPD Markers in Breeding for Disease Resistance in Common Bean

James D. Kelly1* and Phillip N. Miklas2

1Crop and Soil Sciences, Michigan State University,
East Lansing, MI 48824, USA

2USDA-ARS-IAREC, 24106 N. Bunn Rd.,
Prosser WA 99350, USA.

ABSTRACT

Diseases are regarded as the leading constraint to increased common bean (Phaseolus vulgaris) production worldwide. Despite the range in variability and complexity among bean pathogens, single gene and quantitative resistance sources are known. Combining these resistance sources into commercial cultivars is a major challenge for bean breeders. To assist breeders, a major effort to identify RAPD markers tightly linked to different genes was undertaken. To date, 30 RAPD and six SCAR markers linked to 18 different genes have been identified, in addition to QTL conditioning resistance to seven major pathogens of common bean. [A complete list of SCAR markers in beans can be found at P. Miklas’ web site www.usda.prosser.wsu.edu ] We review the feasibility of using marker-assisted selection to incorporate disease resistance into common bean. Indirect selection of single resistance genes in the absence of the pathogen and the opportunity afforded breeders to pyramid these genes to improve their longevity and retain valuable hypostatic genes is discussed. The role of markers linked to the QTL controlling complex resistance and the potential to combine resistance sources using marker based selection is reviewed. Improved levels of selection efficiency are demonstrated using flanking markers, repulsion-phase linkages, co-dominant marker pairs, recombination-facilitated markers and RAPD-derived ASAP and SCAR markers. Marker-assisted selection for disease resistance in common bean clearly provides opportunities to breeders which were not feasible with traditional breeding methods.

Abstracted from: Kelly, J.D., and P.N. Miklas. 1998. The role of RAPD markers in breeding for disease resistance in common bean. Molecular Breeding 4:1-11.


Tagging and Mapping of Genes and QTL and Molecular Marker-Assisted Selection for Traits of Economic Importance in Bean and Cowpea

J. D. Kellya*, P. Geptsb, P.N. Miklasc, and D.P. Coyned

aCrop and Soil Sciences, Michigan State University, East Lansing MI 48824;

* Corresponding author. Tel: 517-355-0205; fax: 517-353-3955. Email address: kellyj@msu.edu

bAgronomy and Range Science, University of California, 1 Shields Avenue, Davis, CA 95616-8515;

cUSDA-ARS-IAREC, 24106 N. Bunn Rd., Prosser WA 99350;

dDept. of Agronomy and Horticulture, University of Nebraska, Lincoln, NE 68583

Key words: domestication, disease resistance, epistasis, indirect selection, introgression, linkage, pathogens, Phaseolus vulgaris, plant breeding, Vigna unguiculata

ABSTRACT

Bean/Cowpea Collaborative Research Support Program (B/C CRSP) scientists have successfully developed integrated consensus maps of the 11 linkage groups in both bean (Phaseolus vulgaris L.) and cowpea (Vigna unguiculata L. Walp). The bean map is approximately 1200 cM with some 500 markers and an additional 500 markers shared with other bean maps. The cowpea map spans 2670 cM with over 400 markers. In addition to molecular markers, both maps include map locations of defense genes and phenotypic traits for disease and insect resistance, seed size, color and storage proteins, pod color and those traits associated with the domestication syndrome in bean. Since the bean and cowpea maps were developed independently, linkage groups with the same number probably refer to non-syntenic groups. Map locations of major resistance genes in bean are revealing gene clusters on linkage groups B1, B4, B7, and B11 for resistance to bean rust, anthracnose, common bacterial blight and white mold. Gene tagging and marker assisted selection for disease resistance has progressed to a point where the indirect selection for resistance to a number of major diseases is now routine in bean breeding programs both in the U.S. and overseas.

Abstracted from: Kelly, J.D., P. Gepts, P.N. Miklas, and D.P. Coyne. 2003. Tagging and mapping of genes and QTL and molecular marker-assisted selection for traits of economic importance in bean and cowpea. Field Crops Res. 82:135-154.

Table 1. RAPD markers linked to major disease resistance genes in common bean.


Resistance genes Germplasm source Gene pool1 Pathogen2 RAPD marker3 Size (bp) Linkage distance (cM) & orientation4
Ur-3 NEP-II

Sierra

MA

MA

Rust OK14

OG15

OL16

 620

1600

1000

2.23 coupling-phase

7.9 coupling-phase

Ur-32 PI 181996

 

MA Rust OAC20

OAE19

 490

 890

No recombinants

6.2 repulsion-phase

Ur-4 Early Gallatin Andean Rust OA14 1100 No recombinants
Ur-5

 

Mexico309

 

MA  Rust OF10

OI19

 970

 460

2.15 coupling-phase

No recombinants

Ur-6 Olathe Andean Rust OV12  950 10.4 coupling-phase5
Ur-9 Pompadour Checa Andean Rust OJ13 1800 5.0 coupling-phase5
Co-1 Michigan DRK Andean Anthracnose OF10  530 1.9 repulsion-phase
Co-2 Cornell 49-242 MA Anthracnose OQ4

B355

OH20

1440

1000

 450

2.0 - 5.5 coupling-phase

5.4 - 7.7 flanking marker

Co-dominant SCAR

Co-42 SEL 1308

G 2333

MA Anthracnose OAS13

OAL9

SAS13

950

740

950

No recombinants

3.1 - 4.5 coupling-phase

SCAR

Co-5 TU, G 2333

SEL 1360

MA Anthracnose OAB3  450 5.9 coupling-phase

 

Co-6 AB136, Catrachita MA Anthracnose OAH1

OAK20

 780

 890

12.3 flanking & co-dominant

 7.3 repulsion-phase

I Seafarer

Montcalm

MA

Andean

BCMV OW13  690 1.3 - 5.0 coupling-phase

Dominant SCAR

bc-3 B85009

MCM3031

MCR2205

MA

MA

Andean

BCMV OAD19

OS13

OC20

OC11

OC11

 690

 660

 460

 350

 420

1.9 repulsion-phase

7.1 coupling-phase

No recombinants, repulsion

No recombinants,

co-dominant, SCAR

bc-12 Olathe MA BCMV OY6

OH19

1200

1000

26.8 coupling-phase5

16.3 flanking markers

bc-u Olathe MA BCMV OG15

OC4

1600

1300

29.4 coupling-phase5

31.6 flanking markers

bgm-1 Garrapato,

A429

MA BGMV OR2

OR2

530

570

4.2 repulsion-phase

coupling & co-dominant

Mp-1

Mp-2

BAT 477

BAT 477

MA

MA

Macrophomina B386

B459

 900

1600

coupling-phase

repulsion-phase


1 MA, Middle American;2 BCMV, Bean Common Mosaic Virus; BGMV, Bean Golden Mosaic Virus; 3 >O= and >B= were derived by decamer primers from Operon Technologies (Alameda, CA) and the University of British Columbia (Vancouver, Canada), respectively;4 SCAR, Sequence Characterized Amplified Region; 5 Recombination within a RIL mapping population, all other represent linkage distances with F2 segregating populations.

MarkersFig1.pdf




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