Eukaryotic Cell
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
EC.00401-06v1
6/8/1299    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Krajaejun, T.
Right arrow Articles by Klein, B. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Krajaejun, T.
Right arrow Articles by Klein, B. S.

 Previous Article  |  Next Article 

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.

Development and Application of a Green Fluorescent Protein Sentinel System for Identification of RNA Interference in Blastomyces dermatitidis Illuminates the Role of Septin in Morphogenesis and Sporulation{triangledown} ,{dagger}

T. Krajaejun,1 G. M. Gauthier,3 C. A. Rappleye,5 T. D. Sullivan,2 and B. S. Klein1,2,3,4*

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.


* Corresponding author. Mailing address: University of Wisconsin—Madison, 600 Highland Ave., K4/434, Madison, WI 53792. Phone: (608) 263-9217. Fax: (608) 263-6210. E-mail: bsklein{at}wisc.edu

{triangledown} Published ahead of print on 11 May 2007.

{dagger} Supplemental material for this article may be found at http://ec.asm.org/.


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.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Appl. Environ. Microbiol. Infect. Immun. J. Bacteriol.
Mol. Cell Biol. Microbiol. Mol. Biol. Rev. ALL ASM JOURNALS
Copyright © 2007 by the American Society for Microbiology.