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Vol. 14, Issue 1, 14-25, January 2003
Department of Biology, Clark University, Worcester,
Massachusetts 01610
Here, we describe the identification and characterization of the
cytokinesis-deficient mutant cell line 17HG5, which was generated in a
restriction enzyme-mediated integration mutagenesis screen designed to
isolate genes required for cytokinesis in Dictyostelium discoideum. Phenotypic characterization of the 17HG5 cell line revealed no apparent defects in the global functionality of the actomyosin cytoskeleton except for the observed cytokinesis defect when
grown in suspension culture. Plasmid rescue was used to identify the
disrupted gene locus (pats1; protein associated with the transduction of signal 1) that caused the cytokinesis defect. Disruption of the
pats1 locus was recreated through homologous recombination in several
independent cell lines, each recapitulating the cytokinesis-defective phenotype and thereby confirming that this gene locus is important for
proper cytokinesis. Sequence data obtained by analysis of the genomic
region flanking the inserted restriction enzyme-mediated integration
plasmid revealed an 8892-bp genomic open reading frame encoding a
2964-amino-acid protein. The putative pats1 protein contains 3 regulatory domains (RI-phosphatase, RII-GTP-binding, R-III protein
kinase), 13 leucine-rich repeats, and 8 WD-40 repeats. These regulatory
domains coupled with the protein-protein interacting domains suggest
that pats1 is involved in signal transduction during cytokinesis in
Dictyostelium.
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