Genetic Linkage Mapping of Allozyme Loci in Even- and Odd-year Pink Salmon (Oncorhynchus gorbuscha)

We constructed genetic linkage maps of allozyme loci in even- and odd-year pink salmon (Oncorhynchus gorbuscha), using the total of 320 families (each female was crossed with two different males, and 80 females and 160 males were used for each of even year and odd year). The maps include eight linka...

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Bibliographic Details
Main Authors: M. P. Matsuoka, A. J. Gharrett, R. L. Wilmot, W. W. Smoker
Other Authors: The Pennsylvania State University CiteSeerX Archives
Format: Text
Language:English
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Online Access:http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.495.2042
http://jhered.oxfordjournals.org/content/95/5/421.full.pdf
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Summary:We constructed genetic linkage maps of allozyme loci in even- and odd-year pink salmon (Oncorhynchus gorbuscha), using the total of 320 families (each female was crossed with two different males, and 80 females and 160 males were used for each of even year and odd year). The maps include eight linkage groups involving 22 loci. We observed substantial variation in recombination frequencies among different families within broodline and between sexes within broodlines. In the linkage analysis between sAAT-3 * and sMDH-B1,2*, two even-year families and one odd-year family exhibited evidence of association, but two even-year and one odd-year families did not. Recombination rate tends to be reduced in males in pink salmon. The ratio of recombination rate (female/male), which ranged from 1.7 to infinity, averaged 2.8 in the even-year crosses and 3.2 in the odd-year crosses. The linkage groups (LG) I and II involving sAAT and mAH loci, which probably duplicated in the recent tetraploidization event, and the orders of loci in the LGs I (sAAT-3*fi mAH-4*) and II (mAH-3* fi sAAT-4*) were reversed, suggesting the possible paracentric inversion during salmonid evolution after the duplication. A linkage map can be constructed with information from joint segregation analysis and gene-centromere (G-C) distances. G-C distance can be estimated in gynogenetic progeny as the recombination frequency between a centro-