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A high-density linkage map with 2560 markers and its application for the localization of the male-sterile genes ms3 and ms4 in Cryptomeria japonica D. Don
Authors:Yoshinari Moriguchi  Kentaro Uchiyama  Saneyoshi Ueno  Tokuko Ujino-Ihara  Asako Matsumoto  Junji Iwai  Daisuke Miyajima  Maki Saito  Masaya Sato  Yoshihiko Tsumura
Affiliation:1.Graduate School of Science and Technology,Niigata University,Nishi-ku,Japan;2.Department of Forest Genetics,Forestry and Forest Products Research Institute,Tsukuba,Japan;3.Niigata Prefectural Forest Research Institute,Murakami,Japan;4.Toyama Prefectural Agricultural Forestry and Fisheries Research Center,Forestry Research Institute,Nakashinkawagun,Japan;5.Faculty of Agriculture,Niigata University,Nishi-ku,Japan;6.Faculty of Life and Environmental Sciences,University of Tsukuba,Tsukuba,Japan
Abstract:Cryptomeria japonica pollinosis is one of the most serious allergic diseases in Japan; this is a social problem because C. japonica is the most important Japanese forestry species. In order to reduce the amount of pollen dispersed, breeding programs using trees with male-sterile genes have been implemented. High-density linkage maps with stable ordering of markers facilitate the localization of male-sterile genes and the construction of partial linkage maps around them in order to develop markers for use in marker-assisted selection. In this study, a high-density linkage map for C. japonica with 2560 markers was constructed. The observed map length was 1266.2 cM and the mean distance between adjacent markers was 0.49 cM. Using information from this high-density map, we newly located two male-sterile genes (ms3 and ms4) on the first and fourth linkage groups, respectively, and constructed partial linkage maps around these loci. We also constructed new partial linkage maps around the ms1 and ms2 loci using additional SNP markers. The closest markers to the ms1, ms2, ms3, and ms4 male-sterile loci were estSNP04188 (1.8 cM), estSNP00695 (7.0 cM), gSNP05415 (3.1 cM), and estSNP01408 (7.0 cM) respectively. These results allowed us to develop SNP markers tightly linked to the male sterile genes for use in MAS; this will accelerate the future isolation of these genes by map-based cloning approaches.
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