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Fine Mapping of Leaf Rust Resistance Gene LrZH84 Using Expressed Sequence Tag and Sequence-Tagged Site Markers, and Allelism with Other Genes on Wheat Chromosome 1B

February 2013 , Volume 103 , Number  2
Pages  169 - 174

Yue Zhou, Xianchun Xia, Zhonghu He, Xing Li, Zaifeng Li, and Daqun Liu

First author: Department of Plant Pathology, College of Plant Protection, Agricultural University of Hebei, Biological Control Center for Plant Diseases and Plant Pests of Hebei, 289 Lingyusi Street, Baoding 071001, Hebei, China; second author: Institute of Crop Science, National Wheat Improvement Center, Chinese Academy of Agricultural Sciences, 12 Zhongguancun South Street, Beijing 100081, China; third author: Institute of Crop Science, National Wheat Improvement Center, Chinese Academy of Agricultural Sciences and CIMMYT China Office, 12 Zhongguancun South Street, Beijing 100081, China; and fourth, fifth, and sixth authors: Department of Plant Pathology, College of Plant Protection, Agricultural University of Hebei, Biological Control Center for Plant Diseases and Plant Pests of Hebei, 289 Lingyusi Street, Baoding 071001, Hebei, China.


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Accepted for publication 28 September 2012.
ABSTRACT

Zhou 8425B, possessing the leaf rust resistance gene LrZH84, is an elite wheat (Triticum aestivum) parental line in the Yellow-Huai Valley region of China. In the present study, 2,086 F2 plants derived from Zhou 8425B/Chinese Spring were used for fine mapping of LrZH84 with expressed sequence tag (EST) and sequence-tagged site (STS) markers. Seventy inter-simple sequence repeat EST and STS markers on 1BL were used to screen the two parents and resistant and susceptible bulks; those polymorphic were used to analyze the entire F2 population. Three EST markers (BF474863, BE497107, and CD373538) were closely linked to LrZH84, with genetic distances of 0.7, 0.7, and 1.7 cM, respectively. STS marker Hbsf-1 was developed from the sequences of polymerase chain reaction fragments amplified from EST marker BF474863. LrZH84 was 8.19 cM proximal to Lr44, but may be allelic to LrXi and LrG98 although they showed different reactions with some Puccinia triticina pathotypes.


Additional keywords: allelism test, genetic mapping, molecular markers.

© 2013 The American Phytopathological Society