April
2004
, Volume
94
, Number
4
Pages
320
-
325
Authors
Richard C.
Larsen
and
Phillip N.
Miklas
Affiliations
U.S. Department of Agriculture-Agriculture Research Service, Vegetable and Forage Crop Research Unit, 24106 North Bunn Road, Prosser, WA 99350
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Accepted for publication 9 December 2003.
Abstract
ABSTRACT
A random amplified polymorphic DNA (RAPD) marker directly linked (0.0 cM) with a resistance gene was identified in a snap bean recombinant inbred population (Moncayo × Primo) consisting of 94 F5:7 recombinant inbred lines that had uniform segregation for disease reaction to Beet curly top virus (BCTV) across three field locations. Resistance was conditioned by a single dominant allele tentatively designated Bct. Seven hundred and fifty decamer primers were screened to obtain the linked RAPD marker that was then converted to a sequence characterized amplified region (SCAR) marker SAS8.1550. The SCAR mapped within a cluster of resistance genes on linkage group B7 of the core map. A survey of 103 BCTV-resistant and -susceptible snap and dry bean genotypes was conducted using SAS8.1550. Results showed that the SCAR would be highly useful for marker-assisted selection of Bct in snap and dry bean originating from the Andean gene pool. Marker-assisted selection for Bct will expedite the development of BCTV-resistant cultivars and minimize the need for cumbersome pathogen tests.
JnArticleKeywords
Additional keywords:
begomovirus,
bulked-segregant analysis,
polymerase chain reaction-based DNA marker.
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ArticleCopyright
The American Phytopathological Society, 2004