Genetics, Vol. 163, 699-710, February 2003, Copyright © 2003

A Linkage Map of an F2 Hybrid Population of Antirrhinum majus and A. molle

Zsuzsanna Schwarz-Sommera, Eugenia de Andrade Silvaa, Rita Berndtgena, Wolf-Ekkehard Lönniga, Andreas Müllera, Ingo Nindla, Kurt Stübera, Jörg Wundera, Heinz Saedlera, Thomas Gübitzb, Amanda Borkingb, John F. Golzb, Enrique Ritterc, and Andrew Hudsonb
a Max Planck Institut für Züchtungsforschung, Carl-von-Linné-Weg 10, 50829 Köln, Germany,
b Institute of Cell and Molecular Biology, University of Edinburgh, Edinburgh EH9 3JH, United Kingdom
c Neiker, 01080 Vitoria, Spain

Corresponding author: Andrew Hudson, University of Edinburgh, King's Bldgs., Mayfield Rd., Edinburgh EH9 3JH, UK., andrew.hudson{at}ed.ac.uk (E-mail)

Communicating editor: V. L. CHANDLER

To increase the utility of Antirrhinum for genetic and evolutionary studies, we constructed a molecular linkage map for an interspecific hybrid A. majus x A. molle. An F2 population (n = 92) was genotyped at a minimum of 243 individual loci. Although distorted transmission ratios were observed at marker loci throughout the genome, a mapping strategy based on a fixed framework of codominant markers allowed the loci to be placed into eight robust linkage groups consistent with the haploid chromosome number of Antirrhinum. The mapped loci included 164 protein-coding genes and a similar number of unknown sequences mapped as AFLP, RFLP, ISTR, and ISSR markers. Inclusion of sequences from mutant loci allowed provisional alignment of classical and molecular linkage groups. The total map length was 613 cM with an average interval of 2.5 cM, but most of the loci were aggregated into clusters reducing the effective distance between markers. Potential causes of transmission ratio distortion and its effects on map construction were investigated. This first molecular linkage map for Antirrhinum should facilitate further mapping of mutations, major QTL, and other coding sequences in this model genus.





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