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203 Swingle Hall, Department of Fisheries and Allied Aquaculture, Auburn University, Auburn, AL 36849
The chromosome number (2N) of ictalurid catfish in North America ranges
from 40 to 72 with the two major aquaculture species, channel catfish
(Ictalurus punctatus) and blue catfish (I. furcatus), having virtually
identical karyotypes (2N = 58). The haploid genome size of channel
catfish is approximately a billion base pairs. Although several genes
important for growth, reproduction, and disease defense have been isolated
from catfish, genetic linkage mapping in catfish is at the initial stage.
Six linkage groups have been established utilizing isozymes. Catfish vary
considerably for quantitative traits. Genetic variability has been
detected at 70 isozyme loci for catfish. Large numbers of polymorphic
markers have been recently developed including 700 random amplification of
polymorphic DNA (RAPD), 1200 amplified fragment length polymorphism
(AFLP), and over 300 microsatellite markers, available for construction of
the catfish genetic linkage map. Reference mapping populations using
channel catfish x blue catfish hybrid system have been produced at Auburn
University, and reference families using channel catfish intraspecific
mating plans have been produced in the USDA ARS Catfish Genetics Research
Unit at Stoneville, for both quantitative traits (QTLs) and genetic
linkage analysis. Important catfish QTLs include disease resistance, feed
conversion efficiency, growth rate, processing yields, tolerance to low
oxygen and low water quality, and seinability. The genetic linkage and
QTL mapping is important for both marker-assisted selection (MAS) and for
isolation of economically important genes from catfish. Progress and
arrangements for collaboration in construction of the catfish genetic map
will be discussed.