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Theor Appl Genet (2013) 126:2451–2465
DOI 10.1007/s00122-013-2146-1
ORIGINAL PAPER
Increasing the density of markers around a major QTL
controlling resistance to angular leaf spot in common bean
Paula Rodrigues Oblessuc · Juliana Morini Kupper Cardoso Perseguini · Renata Moro Baroni ·
Alisson Fernando Chiorato · Sérgio Augusto Morais Carbonell · Jorge Mauricio Costa Mondego ·
Ramon Oliveira Vidal · Luis Eduardo Aranha Camargo · Luciana Lasry Benchimol-Reis
Received: 1 February 2013 / Accepted: 14 June 2013 / Published online: 6 July 2013
© Springer-Verlag Berlin Heidelberg 2013
3.0 cM. The position of the SSR ATA220 coincided with the
maximum LOD score of the QTL. Moreover, a new QTL
(ALS10.2
UC
) was identified at the end of the same link-
age group. Sequence analysis using the P. vulgaris genome
located ten SSRs and seven STS-DArT on chromosome 10
(Pv10). Coincident linkage and genome positions of five
markers enabled the definition of a core region for ALS10.1
spanning 5.3 Mb. These markers are linked to putative
genes related to disease resistance such as glycosyl trans-
ferase, ankyrin repeat-containing, phospholipase, and squa-
mosa-promoter binding protein. Synteny analysis between
ALS10.1 markers and the genome of soybean suggested a
dynamic evolution of this locus in the common bean. The
present study resulted in the identification of new candidate
genes and markers closely linked to a major ALS disease
resistance QTL, which can be used in marker-assisted selec-
tion, fine mapping and positional QTL cloning.
Abstract Angular leaf spot (ALS) causes major yield
losses in the common bean (Phaseolus vulgaris L.), an
important protein source in the human diet. This study
describes the saturation around a major quantitative trait
locus (QTL) region, ALS10.1, controlling resistance to ALS
located on linkage group Pv10 and explores the genomic
context of this region using available data from the P. vul-
garis genome sequence. DArT-derived markers (STS-DArT)
selected by bulk segregant analysis and SCAR and SSR
markers were used to increase the resolution of the QTL,
reducing the confidence interval of ALS10.1 from 13.4 to
Communicated by B. Diers.
Electronic supplementary material The online version of this
article (doi:10.1007/s00122-013-2146-1) contains supplementary
material, which is available to authorized users.
P. R. Oblessuc (*) · J. M. K. Cardoso Perseguini · R. M. Baroni
Departamento de Genética e Evolução e Bioagentes, Instituto
de Biologia, Universidade Estadual de Campinas (UNICAMP),
Campinas, São Paulo 13083-970, Brazil
e-mail: parobl@gmail.com
J. M. K. Cardoso Perseguini
e-mail: jukupper@gmail.com
R. M. Baroni
e-mail: renatabaroni19@gmail.com
P. R. Oblessuc · J. M. K. Cardoso Perseguini · R. M. Baroni ·
J. M. C. Mondego · L. L. Benchimol-Reis
Centro de Recursos Genéticos Vegetais, Instituto Agronômico de
Campinas (IAC), Campinas, São Paulo 13001-970, Brazil
J. M. C. Mondego
e-mail: jmcmondego@iac.sp.gov.br
L. L. Benchimol-Reis
e-mail: llasry@iac.sp.gov.br
A. F. Chiorato · S. A. M. Carbonell
Centro de Grãos e Fibras, Instituto Agronômico de Campinas
(IAC), Campinas, São Paulo 13001-970, Brazil
e-mail: afchiorato@iac.sp.gov.br
S. A. M. Carbonell
e-mail: carbonel@iac.sp.gov.br
R. O. Vidal
CHU Sainte-Justine Research Center,
Université de Montréal,
Montréal, QC, Canada
e-mail: ramon.vidal@gmail.com
L. E. A. Camargo
Departamento de Fitopatologia e Nematologia,
Universidade de São Paulo, Escola Superior de Agricultura
Luiz de Queiroz (USP-ESALQ), Piracicaba,
São Paulo 13418-900, Brazil
e-mail: leacamar@usp.br