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Characterization and in vivo regulon determination of an ECF sigma factor and its cognate anti‐sigma factor in Nostoc punctiforme
Author(s) -
Bell Nicole,
Lee Jamie J.,
Summers Michael L.
Publication year - 2017
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/mmi.13620
Subject(s) - biology , sigma factor , regulon , microbiology and biotechnology , mutant , transcription factor , promoter , gene expression , genetics , gene
Summary Based on primary sequence comparisons and genomic context, Npun_F4153 (SigG)/Npun_F4154 (SapG) of the cyanobacterium Nostoc punctiforme were hypothesized to encode an ECF sigma factor/anti‐sigma factor pair. Transcription of sigG increased in heterocysts and akinetes, and after EDTA treatment. Interaction between SigG and the predicted cytoplasmic domain of SapG was observed in vitro . A SigG‐GFP translational fusion protein localized to the periphery of vegetative cells in vivo , but lost this association following heat stress. A sigG mutant was unable to survive envelope damage caused by heat or EDTA, but was able to form functional heterocysts. Akinetes in the mutant strain appeared normal, but these cultures were less resistant to lysozyme and cold treatments than those of the wild‐type strain. The SigG in vivo regulon was determined before and during akinete differentiation using DNA microarray analysis, and found to include multiple genes with putative association to the cell envelope. Mapped promoters common to both arrays enabled identification of a SigG promoter‐binding motif that was supported in vivo by reporter studies, and in vitro by run‐off transcription experiments. These findings support SigG/SapG as a sigma/anti‐sigma pair involved in repair of envelope damage resulting from exogenous sources or cellular differentiation.