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Linkage analysis of the myosin heavy chain gene in Dictyostelium discoideum using a mutation generated by homologous recombination
Authors:Dennis L Welker  Arturo De Lozanne and James A Spudich
Institution:(1) Molecular Biology/Biochemistry Program, Department of Biology, Utah State University, 84322-5500 Logan, UT, USA;(2) Department of Cell Biology, Stanford University School of Medicine, 94305 Stanford, CA, USA;(3) Present address: Department of Molecular Genetics, University of Texas, Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, 75235 Dallas, TX, USA
Abstract:Summary A mutation (mhcA1 in strain HMM) created by insertional gene inactivation was used to map the Dictyostelium discoideum myosin heavy chain gene (mhcA) to linkage group IV. Three phenotypic traits associated with this mutation (slow colony growth, inability of the mutant to develop past aggregation, and the presence of five to ten integrated vector copies) cosegregated as expected for the consequences of a single insertional event. This linkage was confirmed using a restriction fragment length polymorphism. The mhcA1 mutation was recessive to wild type and was nonallelic with mutations at the following loci on linkage group IV: aggJ, aggL, couH, minA, phgB and tsgB. This work demonstrates the ability to apply standard techniques developed for D. discoideum parasexual genetic analyses to mutants generated by transformation, which is of particular relevance to analysis of genes for which no classical mutations or restriction fragment length polymorphisms are available.
Keywords:Dictyostelium discoideum  Myosin  Linkage analysis  Gene disruption
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