Genetics, Vol. 165, 1551-1568, November 2003, Copyright © 2003
A Consensus Linkage Map for Sugi (Cryptomeria japonica) From Two Pedigrees, Based on Microsatellites and Expressed Sequence Tags
Naoki Tania,
Tomokazu Takahashib,
Hiroyoshi Iwataa,
Yuzuru Mukaic,
Tokuko Ujino-Iharaa,
Asako Matsumotoa,
Kensuke Yoshimuraa,
Hiroshi Yoshimarua,
Masafumi Muraia,
Kazutoshi Nagasakaa, and
Yoshihiko Tsumuraa
a Department of Forest Genetics, Forestry and Forest Products Research Institute, Tsukuba, Ibaraki 305-8687, Japan,
b Graduate School of Science and Technology, Niigata University, Igarashi, Niigata 950-2181, Japan
c Faculty of Agriculture, Shizuoka University, Ohya, Shizuoka 422-8529, Japan
Corresponding author:
Yoshihiko Tsumura, Forestry and Forest Products Research Institute, Tsukuba, Ibaraki 305-8687, Japan., ytsumu{at}ffpri.affrc.go.jp (E-mail)
Communicating editor: S. MCCOUCH
A consensus map for sugi (Cryptomeria japonica) was constructed by integrating linkage data from two unrelated third-generation pedigrees, one derived from a full-sib cross and the other by self-pollination of F1 individuals. The progeny segregation data of the first pedigree were derived from cleaved amplified polymorphic sequences, microsatellites, restriction fragment length polymorphisms, and single nucleotide polymorphisms. The data of the second pedigree were derived from cleaved amplified polymorphic sequences, isozyme markers, morphological traits, random amplified polymorphic DNA markers, and restriction fragment length polymorphisms. Linkage analyses were done for the first pedigree with JoinMap 3.0, using its parameter set for progeny derived by cross-pollination, and for the second pedigree with the parameter set for progeny derived from selfing of F1 individuals. The 11 chromosomes of C. japonica are represented in the consensus map. A total of 438 markers were assigned to 11 large linkage groups, 1 small linkage group, and 1 nonintegrated linkage group from the second pedigree; their total length was 1372.2 cM. On average, the consensus map showed 1 marker every 3.0 cM. PCR-based codominant DNA markers such as cleaved amplified polymorphic sequences and microsatellite markers were distributed in all linkage groups and occupied about half of mapped loci. These markers are very useful for integration of different linkage maps, QTL mapping, and comparative mapping for evolutional study, especially for species with a large genome size such as conifers.
