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Journal of Bacteriology, April 2001, p. 2654-2661, Vol. 183, No. 8
Section of Microbiology, Division of
Biological Sciences, University of California, Davis, California
95616
Received 4 December 2000/Accepted 26 January 2001
A novel gene, hetF, was identified as essential for
heterocyst development in the filamentous cyanobacterium Nostoc
punctiforme strain ATCC 29133. In the absence of combined
nitrogen, hetF mutants were unable to differentiate
heterocysts, whereas extra copies of hetF in
trans induced the formation of clusters of heterocysts. Sequences hybridizing to a hetF probe were detected only in
heterocyst-forming cyanobacteria. The inactivation and multicopy
effects of hetF were similar to those of hetR,
which encodes a self-degrading serine protease thought to be a central
regulator of heterocyst development. Increased transcription of
hetR begins in developing cells 3 to 6 h after
deprivation for combined nitrogen (N step-down), and the HetR protein
specifically accumulates in heterocysts. In the hetF
mutant, this increase in hetR transcription was delayed, and a hetR promoter::green fluorescent protein
(GFP) transcriptional reporter indicated that increased transcription
of hetR occurred in all cells rather than only in
developing heterocysts. When a fully functional HetR-GFP fusion protein
was expressed in the hetF mutant from a multicopy plasmid,
HetR-GFP accumulated nonspecifically in all cells under
nitrogen-replete conditions; when expressed in the wild type, HetR-GFP
was observed only in heterocysts after N step-down. HetF therefore
appears to cooperate with HetR in a positive regulatory pathway and may
be required for the increased transcription of hetR and
localization of the HetR protein in differentiating heterocysts.
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.8.2654-2661.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
The hetF Gene Product Is Essential to Heterocyst
Differentiation and Affects HetR Function in the
Cyanobacterium Nostoc punctiforme
*
Corresponding author. Mailing address: Section of
Microbiology, University of California, Davis, One Shields Avenue,
Davis, CA 95616. Phone: (530) 752-3346. Fax: (530) 752-9014. E-mail: jcmeeks{at}ucdavis.edu.
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