Affiliation:
1. Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, 2781-901 Oeiras Codex, Portugal
2. Department of Microbiology, Emory University School of Medicine, Atlanta, Georgia 30322
Abstract
ABSTRACT
RNA polymerase sigma factor σ
F
initiates the prespore-specific program of gene expression during
Bacillus subtilis
sporulation. σ
F
governs transcription of
spoIIIG
, encoding the late prespore-specific regulator σ
G
. However, transcription of
spoIIIG
is delayed relative to other genes under the control of σ
F
, and after synthesis, σ
G
is initially kept in an inactive form. Activation of σ
G
requires the complete engulfment of the prespore by the mother cell and expression of the
spoIIIA
and
spoIIIJ
loci. We screened for random mutations in
spoIIIG
that bypassed the requirement for
spoIIIA
for the activation of σ
G
. We found a mutation (
spoIIIGE156K
) that resulted in an amino acid substitution at position 156, which is adjacent to the position of a mutation (E155K) previously shown to prevent interaction of SpoIIAB with σ
G
. Comparative modelling techniques and in vivo studies suggested that the
spoIIIGE156K
mutation interferes with the interaction of SpoIIAB with σ
G
. The σ
GE156K
isoform restored σ
G
-directed gene expression to
spoIIIA
mutant cells. However, expression of
sspE
-
lacZ
in the
spoIIIA spoIIIGE156K
double mutant was delayed relative to completion of the engulfment process and was not confined to the prespore. Rather, β-galactosidase accumulated throughout the entire cell at late times in development. This suggests that the activity of σ
GE156K
is still regulated in the prespore of a
spoIIIA
mutant, but not by SpoIIAB. In agreement with this suggestion, we also found that expression of
spoIIIGE156K
from the promoter for the early prespore-specific gene
spoIIQ
still resulted in
sspE-lacZ
induction at the normal time during sporulation, coincidently with completion of the engulfment process. In contrast, transcription of
spoIIIGE156K
, but not of the wild-type
spoIIIG
gene, from the mother cell-specific
spoIID
promoter permitted the rapid induction of
sspE-lacZ
expression. Together, the results suggest that SpoIIAB is either redundant or has no role in the regulation of σ
G
in the prespore.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Reference52 articles.
1. Campbell, E. A., and S. A. Darst. 2000. The anti-σ factor SpoIIAB forms a 2:1 complex with σF, contacting multiple conserved regions of the σ factor. J. Mol. Biol. 300 : 17-28.
2. Campbell, E. A., S. Masuda, J. L. Sun, O. Muzzin, C. A. Olson, S. Wang, and S. A. Darst. 2002. Crystal structure of the Bacillus stearothermophilus anti-σ factor SpoIIAB with the sporulation factor σF. Cell 108 : 795-807.
3. Deletion of spoIIAB blocks endospore formation in Bacillus subtilis at an early stage
4. Cutting, S. M., and P. B. V. Horn. 1990. Genetics analysis, p. 27-74. In C. R. Harwood and S. M. Cutting (ed.), Molecular biological methods for Bacillus . John Wiley & Sons Ltd., Chichester, England.
5. Decatur, A., and R. Losick. 1996. Multiple sites of contact between the Bacillus subtilis developmental transcription factor σF and its anti-sigma factor SpoIIAB. Genes Dev. 10 : 2348-2358.
Cited by
31 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献