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United States Department of Agriculture

Agricultural Research Service


item Phillips, Ruth
item Noakes, Marc
item Dekoning, Jenefer
item Morasch, Matthew
item Keatley, Kimberly
item Rexroad, Caird
item Palti, Yniv
item Danzmann, Roy
item Nichols, Krista
item Drew, Robert
item Thorgaard, Gary

Submitted to: Plant and Animal Genome VX Conference Abstracts
Publication Type: Abstract Only
Publication Acceptance Date: 3/19/2005
Publication Date: 3/19/2005
Citation: Phillips, R., Noakes, M., Dekoning, J., Morasch, M., Keatley, K., Rexroad III, C.E., Palti, Y., Danzmann, R., Nichols, K., Drew, R., Thorgaard, G. 2005. Assignment of rainbow trout linkage groups to specific chromosomes. Plant and Animal Genome XIII Abstracts W034, page 13.

Interpretive Summary:

Technical Abstract: The genetic map of rainbow trout has been linked to specific chromosomes and chromosome arms of the OSU (2N=60) strain using fluorescence in situ hybridization (FISH) with BACs containing markers from each genetic linkage group. These markers included type I genes, microsatellite loci and random BACs linked to the genetic map by SNPs. The resulting cytogenetic map helps explain differences in genetic maps based on crosses with parents of different karyotypes and chromosome-specific variation found in the recombination rates between male and female maps. Chromosome structure has a major effect on recombination rate differences between the sexes. Linkage groups of uni-armed (acrocentric) chromosomes had lower female:male recombination rates than linkage groups of biarmed (metacentric) chromosomes. Localization of selective BACs to chromosomes of hybrids between OSU and Clearwater (2N=58) and OSU and Swanson (2N=58) clonal lines showed that the strains with 58 chromosomes had a chromosome fusion involving chromosome pairs 25 and 29 from the OSU strain. BAC clones were obtained by screening the OSU and Swanson libraries. DNA was extracted, clones labeled using nick translation and hybridizations carried out according to standard methods. Images were captured with a Sensys camera and analyzed with Cytovision software (Applied Imaging, Inc.). Chromosomes were identified by size, chromosome arm ratios and using centromere probes. Supported by Grant 2002-00466 from USDA.

Last Modified: 06/26/2017
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