2002
DOI: 10.1128/jb.184.17.4881-4890.2002
|View full text |Cite
|
Sign up to set email alerts
|

Genome-Wide Analysis of the Stationary-Phase Sigma Factor (Sigma-H) Regulon ofBacillus subtilis

Abstract: Sigma-H is an alternative RNA polymerase sigma factor that directs the transcription of many genes that function at the transition from exponential growth to stationary phase in Bacillus subtilis. Twenty-three promoters, which drive transcription of 33 genes, are known to be recognized by sigma-H-containing RNA polymerase. To identify additional genes under the control of sigma-H on a genome-wide basis, we carried out transcriptional profiling experiments using a DNA microarray containing >99% of the annotated… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

6
305
0
1

Year Published

2003
2003
2018
2018

Publication Types

Select...
5
5

Relationship

1
9

Authors

Journals

citations
Cited by 302 publications
(312 citation statements)
references
References 65 publications
6
305
0
1
Order By: Relevance
“…Cells were harvested, and total RNA was prepared as described in ref. 30. RNA from each sample was reverse-transcribed and labeled with Cy3 or Cy5.…”
Section: Methodsmentioning
confidence: 99%
“…Cells were harvested, and total RNA was prepared as described in ref. 30. RNA from each sample was reverse-transcribed and labeled with Cy3 or Cy5.…”
Section: Methodsmentioning
confidence: 99%
“…To induce the synthesis of KinA, KinC, their mutant proteins, or their fusion proteins with GFP, each of these genes was placed under the control of the Phy-spank promoter (Britton et al, 2002). IPTG was added to Luria-Bertani (LB) cultures during the exponential growth phase (OD 600 of 0.5) as the rich medium conditions.…”
Section: Methodsmentioning
confidence: 99%
“…The PCR fragment generated contained the complete mutant yjbH coding sequence with a His 6 tag. The fragment was cleaved with HindIII and NheI, followed by ligation with HindIII/NheI-cleaved pDR111 (Britton et al, 2002). The ligations were used to transform strain DH5a.…”
Section: Methodsmentioning
confidence: 99%