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Eukaryotic Cell, August 2007, p. 1299-1309, Vol. 6, No. 8
1535-9778/07/$08.00+0 doi:10.1128/EC.00401-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
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Departments of Medical Microbiology and Immunology,1 Pediatrics,2 Internal Medicine,3 Comprehensive Cancer Center, University of Wisconsin Medical School, University of Wisconsin Hospital and Clinics, Madison, Wisconsin 53792,4 Department of Microbiology, The Ohio State University, Columbus, Ohio5
Received 16 December 2006/ Accepted 1 May 2007
A high-throughput strategy for testing gene function would accelerate progress in our understanding of disease pathogenesis for the dimorphic fungus Blastomyces dermatitidis, whose genome is being completed. We developed a green fluorescent protein (GFP) sentinel system of gene silencing to rapidly study genes of unknown function. Using Gateway technology to efficiently generate RNA interference plasmids, we cloned a target gene, "X," next to GFP to create one hairpin to knock down the expression of both genes so that diminished GFP reports target gene expression. To test this approach in B. dermatitidis, we first used LACZ and the virulence gene BAD1 as targets. The level of GFP reliably reported interference of their expression, leading to rapid detection of gene-silenced transformants. We next investigated a previously unstudied gene encoding septin and explored its possible role in morphogenesis and sporulation. A CDC11 septin homolog in B. dermatitidis localized to the neck of budding yeast cells. CDC11-silenced transformants identified with the sentinel system grew slowly as flat or rough colonies on agar. Microscopically, they formed ballooned, distorted yeast cells that failed to bud, and they sporulated poorly as mold. Hence, this GFP sentinel system enables rapid detection of gene silencing and has revealed a pronounced role for septin in morphogenesis, budding, and sporulation of B. dermatitidis.
Published ahead of print on 11 May 2007.
Supplemental material for this article may be found at http://ec.asm.org/.
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