NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE206572 Query DataSets for GSE206572
Status Public on Jun 24, 2022
Title MraZ is a transcriptional inhibitor of cell division in Bacillus subtilis
Organism Bacillus subtilis PY79
Experiment type Expression profiling by high throughput sequencing
Summary To investigate the possible genes regulated by the DNA binding protein MraZ
The bacterial division and cell wall (dcw) cluster is a highly conserved region of the genome which encodes several essential cell division factors including the central divisome protein FtsZ. Understanding the regulation of this region is key to our overall understanding of the division process. mraZ is found at the 5’ end of the dcw cluster and previous studies have described MraZ as a sequence-specific DNA binding protein. In this article, we investigate MraZ to elucidate its role in Bacillus subtilis. Through our investigation, we demonstrate that increased levels of MraZ result in lethal filamentation due to repression of its own operon (mraZ-mraW-ftsL-pbpB). We observe rescue of filamentation upon decoupling ftsL expression, but not other genes in the operon, from MraZ control. Our data suggests that regulation of the mra operon may be an alternative way for cells to quickly arrest cytokinesis potentially during entry into stationary phase and in the event of DNA replication arrest. Furthermore, through timelapse microscopy we were able to identify that overexpression of mraZ or depletion of FtsL results in de-condensation of the FtsZ ring (Z-ring). Using fluorescent D-amino acid labelling, we also observed that coordinated peptidoglycan insertion at division site is dysregulated in the absence of FtsL. Thus, we reveal the precise role of FtsL is in Z-ring maturation and focusing septal peptidoglycan synthesis.
 
Overall design Comparative analysis of RNA-seq data of wild type B. subtilis (PY79), del-mraZ (MW192), or overexpression strains of mraZ (MW189) and mutant mraZ-R15A (MW256)
 
Contributor(s) Prahathees E
Citation(s) 35943250
NIH grant(s)
Grant ID Grant title Affiliation Name
R35 GM133617 Division site determination in Gram-positive bacteria UNIVERSITY OF SOUTH FLORIDA Prahathees Jai Eswara
Submission date Jun 21, 2022
Last update date Sep 23, 2022
Contact name Prahathees Eswara
E-mail(s) [email protected]
Organization name University of South Florida
Street address 4202 E Fowler Ave ISA2015
City Tampa
State/province Florida
ZIP/Postal code 33620
Country USA
 
Platforms (1)
GPL32384 NextSeq 2000 (Bacillus subtilis PY79)
Samples (4)
GSM6257029 052821_91 [PY79_S91]
GSM6257030 052821_92 [MW189_S92]
GSM6257031 052821_93 [MW192_S93]
Relations
BioProject PRJNA851398

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE206572_120_Differentially_Expressed_Genes_In_MW256vPY79.tsv.gz 7.7 Kb (ftp)(http) TSV
GSE206572_150_Differentially_Expressed_Genes_In_MW192vPY79.tsv.gz 9.5 Kb (ftp)(http) TSV
GSE206572_766_Differentially_Expressed_Genes_In_MW189vPY79.tsv.gz 45.0 Kb (ftp)(http) TSV
GSE206572_MW189vPY79_All_Quantified_Genes.tsv.gz 229.3 Kb (ftp)(http) TSV
GSE206572_MW192vPY79_All_Quantified_Genes.tsv.gz 199.8 Kb (ftp)(http) TSV
GSE206572_MW256vPY79_All_Quantified_Genes.tsv.gz 197.8 Kb (ftp)(http) TSV
GSE206572_alignment.tsv.gz 207 b (ftp)(http) TSV
GSE206572_hisat2_counts.tsv.gz 42.5 Kb (ftp)(http) TSV
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap