Crisscross regulation of cell-type-specific gene expression during development in B. subtilis.

PubWeight™: 5.05‹?› | Rank: Top 1%

🔗 View Article (PMID 1538747)

Published in Nature on February 13, 1992

Authors

R Losick1, P Stragier

Author Affiliations

1: Department of Cellular and Developmental Biology, Harvard University, Cambridge, Massachusetts 02138.

Articles citing this

(truncated to the top 100)

Bacillus thuringiensis and its pesticidal crystal proteins. Microbiol Mol Biol Rev (1998) 13.47

Surface proteins of gram-positive bacteria and mechanisms of their targeting to the cell wall envelope. Microbiol Mol Biol Rev (1999) 7.76

Bacillus subtilis sporulation: regulation of gene expression and control of morphogenesis. Microbiol Rev (1993) 7.33

The sigma factors of Bacillus subtilis. Microbiol Rev (1995) 5.76

Bacillus subtilis spore coat. Microbiol Mol Biol Rev (1999) 4.21

spo0J is required for normal chromosome segregation as well as the initiation of sporulation in Bacillus subtilis. J Bacteriol (1994) 3.87

Stress-induced activation of the sigma B transcription factor of Bacillus subtilis. J Bacteriol (1993) 3.64

SpoIIAB is an anti-sigma factor that binds to and inhibits transcription by regulatory protein sigma F from Bacillus subtilis. Proc Natl Acad Sci U S A (1993) 3.63

Sigma-B, a putative operon encoding alternate sigma factor of Staphylococcus aureus RNA polymerase: molecular cloning and DNA sequencing. J Bacteriol (1996) 3.58

Use of immunofluorescence to visualize cell-specific gene expression during sporulation in Bacillus subtilis. J Bacteriol (1995) 3.02

Four additional genes in the sigB operon of Bacillus subtilis that control activity of the general stress factor sigma B in response to environmental signals. J Bacteriol (1995) 3.00

Compartmentalization of gene expression during Bacillus subtilis spore formation. Microbiol Mol Biol Rev (2004) 2.96

General stress transcription factor sigmaB and its role in acid tolerance and virulence of Listeria monocytogenes. J Bacteriol (1998) 2.78

Effect of rpoS mutation on the stress response and expression of virulence factors in Pseudomonas aeruginosa. J Bacteriol (1999) 2.72

Temporal competition between differentiation programs determines cell fate choice. Mol Syst Biol (2011) 2.61

A recently evolved transcriptional network controls biofilm development in Candida albicans. Cell (2012) 2.56

Identification of a gene, spoIIR, that links the activation of sigma E to the transcriptional activity of sigma F during sporulation in Bacillus subtilis. Proc Natl Acad Sci U S A (1995) 2.29

Use of green fluorescent protein for visualization of cell-specific gene expression and subcellular protein localization during sporulation in Bacillus subtilis. J Bacteriol (1995) 2.28

Transcription factor sigma B of Bacillus subtilis controls a large stationary-phase regulon. J Bacteriol (1993) 2.18

Disappearance of the sigma E transcription factor from the forespore and the SpoIIE phosphatase from the mother cell contributes to establishment of cell-specific gene expression during sporulation in Bacillus subtilis. J Bacteriol (1997) 2.17

Septal localization of the SpoIIIE chromosome partitioning protein in Bacillus subtilis. EMBO J (1997) 2.09

SpoIIE governs the phosphorylation state of a protein regulating transcription factor sigma F during sporulation in Bacillus subtilis. Proc Natl Acad Sci U S A (1996) 2.03

Gene expression in single cells of Bacillus subtilis: evidence that a threshold mechanism controls the initiation of sporulation. J Bacteriol (1994) 2.02

Secretion, localization, and antibacterial activity of TasA, a Bacillus subtilis spore-associated protein. J Bacteriol (1999) 1.99

Sporulation gene spoIIB from Bacillus subtilis. J Bacteriol (1993) 1.98

Transient gene asymmetry during sporulation and establishment of cell specificity in Bacillus subtilis. Genes Dev (1999) 1.96

Two Anabaena sp. strain PCC 7120 DNA-binding factors interact with vegetative cell- and heterocyst-specific genes. J Bacteriol (1994) 1.96

Bacillus subtilis gtaB encodes UDP-glucose pyrophosphorylase and is controlled by stationary-phase transcription factor sigma B. J Bacteriol (1993) 1.84

CotM of Bacillus subtilis, a member of the alpha-crystallin family of stress proteins, is induced during development and participates in spore outer coat formation. J Bacteriol (1997) 1.77

The Bacillus subtilis sigma(X) protein is an extracytoplasmic function sigma factor contributing to survival at high temperature. J Bacteriol (1997) 1.76

Daptomycin-mediated reorganization of membrane architecture causes mislocalization of essential cell division proteins. J Bacteriol (2012) 1.75

Characterization of cotJ, a sigma E-controlled operon affecting the polypeptide composition of the coat of Bacillus subtilis spores. J Bacteriol (1995) 1.73

Cloning and characterization of a gene required for assembly of the Bacillus subtilis spore coat. J Bacteriol (1993) 1.73

Clostridium difficile spore biology: sporulation, germination, and spore structural proteins. Trends Microbiol (2014) 1.73

General stress transcription factor sigmaB and sporulation transcription factor sigmaH each contribute to survival of Bacillus subtilis under extreme growth conditions. J Bacteriol (1998) 1.72

An additional GerE-controlled gene encoding an abundant spore coat protein from Bacillus subtilis. J Bacteriol (1995) 1.72

A sporulation membrane protein tethers the pro-sigmaK processing enzyme to its inhibitor and dictates its subcellular localization. Genes Dev (2002) 1.68

A Bacillus subtilis secreted protein with a role in endospore coat assembly and function. J Bacteriol (1999) 1.66

Sigma factors, asymmetry, and the determination of cell fate in Bacillus subtilis. Proc Natl Acad Sci U S A (1994) 1.63

Bacillus subtilis spore coat assembly requires cotH gene expression. J Bacteriol (1996) 1.61

Developmental regulation of transcription of whiE, a locus specifying the polyketide spore pigment in Streptomyces coelicolor A3 (2) J Bacteriol (1998) 1.57

Proteolytic processing of the protease which initiates degradation of small, acid-soluble proteins during germination of Bacillus subtilis spores. J Bacteriol (1993) 1.56

Coupling between gene expression and DNA synthesis early during development in Bacillus subtilis. Proc Natl Acad Sci U S A (1992) 1.56

A compartmentalized regulator of developmental gene expression in Bacillus subtilis. J Bacteriol (1996) 1.51

Hierarchical evolution of the bacterial sporulation network. Curr Biol (2010) 1.50

Identification and characterization of the Bacillus subtilis spoIIP locus. J Bacteriol (1995) 1.46

Physical and functional characterization of the Bacillus subtilis spoIIM gene. J Bacteriol (1993) 1.46

Cloning, nucleotide sequence, and regulation of the Bacillus subtilis pbpF gene, which codes for a putative class A high-molecular-weight penicillin-binding protein. J Bacteriol (1993) 1.45

Sporulation and enterotoxin (CPE) synthesis are controlled by the sporulation-specific sigma factors SigE and SigK in Clostridium perfringens. J Bacteriol (2009) 1.45

An early A-signal-dependent gene in Myxococcus xanthus has a sigma 54-like promoter. J Bacteriol (1995) 1.39

Site of phosphorylation of SpoIIAA, the anti-anti-sigma factor for sporulation-specific sigma F of Bacillus subtilis. J Bacteriol (1995) 1.39

A developmental checkpoint couples the initiation of sporulation to DNA replication in Bacillus subtilis. EMBO J (1994) 1.36

The prosequence of pro-sigmaK promotes membrane association and inhibits RNA polymerase core binding. J Bacteriol (1998) 1.36

The dacF-spoIIA operon of Bacillus subtilis, encoding sigma F, is autoregulated. J Bacteriol (1994) 1.34

Krebs cycle function is required for activation of the Spo0A transcription factor in Bacillus subtilis. Proc Natl Acad Sci U S A (1995) 1.34

Novel secretion apparatus maintains spore integrity and developmental gene expression in Bacillus subtilis. PLoS Genet (2009) 1.32

Bacillus subtilis lon protease prevents inappropriate transcription of genes under the control of the sporulation transcription factor sigma G. J Bacteriol (1994) 1.32

Anabaena sp. strain PCC 7120 responds to nitrogen deprivation with a cascade-like sequence of transcriptional activations. J Bacteriol (1997) 1.31

Activation of the proprotein transcription factor pro-sigmaE is associated with its progression through three patterns of subcellular localization during sporulation in Bacillus subtilis. J Bacteriol (1998) 1.30

Sporulation protein SpoIVFB from Bacillus subtilis enhances processing of the sigma factor precursor Pro-sigma K in the absence of other sporulation gene products. J Bacteriol (1995) 1.29

Analysis of the role of prespore gene expression in the compartmentalization of mother cell-specific gene expression during sporulation of Bacillus subtilis. J Bacteriol (1996) 1.27

Characterization of the involvement of two compensatory autolysins in mother cell lysis during sporulation of Bacillus subtilis 168. J Bacteriol (1995) 1.27

Multilevel regulation of the sporulation transcription factor sigma K in Bacillus subtilis. J Bacteriol (1993) 1.27

Contribution of partner switching and SpoIIAA cycling to regulation of sigmaF activity in sporulating Bacillus subtilis. J Bacteriol (1997) 1.23

Membrane topology of the Bacillus subtilis pro-sigma(K) processing complex. J Bacteriol (2000) 1.23

SpoVM, a small protein essential to development in Bacillus subtilis, interacts with the ATP-dependent protease FtsH. J Bacteriol (1997) 1.22

Visualization of differential gene expression by improved cyan fluorescent protein and yellow fluorescent protein production in Bacillus subtilis. Appl Environ Microbiol (2004) 1.21

Cryptic DNA-binding domain in the C terminus of RNA polymerase II general transcription factor RAP30. Proc Natl Acad Sci U S A (1994) 1.21

Adjacent and divergently oriented operons under the control of the sporulation regulatory protein GerE in Bacillus subtilis. J Bacteriol (1995) 1.20

Bacillus subtilis Pro-sigmaE fusion protein localizes to the forespore septum and fails to be processed when synthesized in the forespore. J Bacteriol (1997) 1.19

Analysis by fluorescence microscopy of the development of compartment-specific gene expression during sporulation of Bacillus subtilis. J Bacteriol (1994) 1.19

Evidence that the spoIIM gene of Bacillus subtilis is transcribed by RNA polymerase associated with sigma E. J Bacteriol (1993) 1.16

Overproducing the Bacillus subtilis mother cell sigma factor precursor, Pro-sigma K, uncouples sigma K-dependent gene expression from dependence on intercompartmental communication. J Bacteriol (1994) 1.15

Solution structure of SpoIIAA, a phosphorylatable component of the system that regulates transcription factor sigmaF of Bacillus subtilis. Proc Natl Acad Sci U S A (1998) 1.14

Effects of amino acid substitutions in the -10 binding region of sigma E from Bacillus subtilis. J Bacteriol (1992) 1.13

Mutational analysis of the precursor-specific region of Bacillus subtilis sigma E. J Bacteriol (1992) 1.11

Development of a two-part transcription probe to determine the completeness of temporal and spatial compartmentalization of gene expression during bacterial development. Proc Natl Acad Sci U S A (2001) 1.11

Regulation of Bacillus subtilis sigmaH (spo0H) and AbrB in response to changes in external pH. J Bacteriol (1997) 1.10

Expression of spoIIIJ in the prespore is sufficient for activation of sigma G and for sporulation in Bacillus subtilis. J Bacteriol (2003) 1.08

Genome-wide dynamic transcriptional profiling in Clostridium beijerinckii NCIMB 8052 using single-nucleotide resolution RNA-Seq. BMC Genomics (2012) 1.08

Forespore expression and processing of the SigE transcription factor in wild-type and mutant Bacillus subtilis. J Bacteriol (1998) 1.08

Forespore-specific transcription of the lonB gene during sporulation in Bacillus subtilis. J Bacteriol (2001) 1.07

Reversible and noisy progression towards a commitment point enables adaptable and reliable cellular decision-making. PLoS Comput Biol (2011) 1.06

spoIVH (ykvV), a requisite cortex formation gene, is expressed in both sporulating compartments of Bacillus subtilis. J Bacteriol (2004) 1.06

Sporulation and primary sigma factor homologous genes in Clostridium acetobutylicum. J Bacteriol (1994) 1.04

Control of the expression and compartmentalization of (sigma)G activity during sporulation of Bacillus subtilis by regulators of (sigma)F and (sigma)E. J Bacteriol (2005) 1.03

Analysis of the relationship between the decrease in pH and accumulation of 3-phosphoglyceric acid in developing forespores of Bacillus species. J Bacteriol (1996) 1.02

Identification of additional genes under the control of the transcription factor sigma F of Bacillus subtilis. J Bacteriol (1996) 1.02

Structure of components of an intercellular channel complex in sporulating Bacillus subtilis. Proc Natl Acad Sci U S A (2012) 1.02

Isolation of a Bacillus subtilis spoIIGA allele that suppresses processing-negative mutations in the Pro-sigma E gene (sigE). J Bacteriol (1994) 1.01

Sortase C-mediated anchoring of BasI to the cell wall envelope of Bacillus anthracis. J Bacteriol (2007) 1.00

Transcription of spoIVB is the only role of sigma G that is essential for pro-sigma K processing during spore formation in Bacillus subtilis. J Bacteriol (1995) 1.00

A feedback loop regulates the switch from one sigma factor to the next in the cascade controlling Bacillus subtilis mother cell gene expression. J Bacteriol (1997) 1.00

Deletion of the Bacillus subtilis isocitrate dehydrogenase gene causes a block at stage I of sporulation. J Bacteriol (1997) 0.99

Transcriptional regulation of the Bacillus thuringiensis subsp. thompsoni crystal protein gene operon. J Bacteriol (1993) 0.98

Cell-type specificity during development in Bacillus subtilis: the molecular and morphological requirements for sigma E activation. EMBO J (1995) 0.97

Gene conservation among endospore-forming bacteria reveals additional sporulation genes in Bacillus subtilis. J Bacteriol (2012) 0.97

Role of the sporulation protein BofA in regulating activation of the Bacillus subtilis developmental transcription factor sigmaK. J Bacteriol (1999) 0.97

Alternative translation initiation produces a short form of a spore coat protein in Bacillus subtilis. J Bacteriol (2001) 0.96

In vivo expression of the Bacillus subtilis spoVE gene. J Bacteriol (1993) 0.96

Articles by these authors

Essential Bacillus subtilis genes. Proc Natl Acad Sci U S A (2003) 14.01

Antibiotic-resistance cassettes for Bacillus subtilis. Gene (1995) 7.28

Plasmids for ectopic integration in Bacillus subtilis. Gene (1996) 5.87

Identification of a new sigma-factor involved in compartmentalized gene expression during sporulation of Bacillus subtilis. Genes Dev (1989) 4.18

The spoIIJ gene, which regulates early developmental steps in Bacillus subtilis, belongs to a class of environmentally responsive genes. J Bacteriol (1990) 3.84

Tandem genes encoding sigma-factors for consecutive steps of development in Bacillus subtilis. Genes Dev (1989) 3.77

Activation of cell-specific transcription by a serine phosphatase at the site of asymmetric division. Science (1995) 3.08

A developmental gene product of Bacillus subtilis homologous to the sigma factor of Escherichia coli. Nature (1984) 2.85

Localization of protein implicated in establishment of cell type to sites of asymmetric division. Science (1995) 2.76

The Bacillus subtilis gene for the development transcription factor sigma K is generated by excision of a dispensable DNA element containing a sporulation recombinase gene. Genes Dev (1990) 2.44

Regulation of diaminopimelate decarboxylase synthesis in Escherichia coli. III. Nucleotide sequence and regulation of the lysR gene. J Mol Biol (1983) 2.40

Two functional domains conserved in major and alternate bacterial sigma factors. FEBS Lett (1985) 2.15

SpoIIQ, a forespore-expressed gene required for engulfment in Bacillus subtilis. Mol Microbiol (1997) 2.11

Cell-cell signaling pathway activating a developmental transcription factor in Bacillus subtilis. Genes Dev (1995) 2.07

SpoIIE governs the phosphorylation state of a protein regulating transcription factor sigma F during sporulation in Bacillus subtilis. Proc Natl Acad Sci U S A (1996) 2.03

Transient gene asymmetry during sporulation and establishment of cell specificity in Bacillus subtilis. Genes Dev (1999) 1.96

Nucleotide sequence of the spo0B gene of Bacillus subtilis and regulation of its expression. Proc Natl Acad Sci U S A (1984) 1.90

Regulation of diaminopimelate decarboxylase synthesis in Escherichia coli. II. Nucleotide sequence of the lysA gene and its regulatory region. J Mol Biol (1983) 1.85

Developmental regulation of transcription of the Bacillus subtilis ftsAZ operon. J Mol Biol (1992) 1.83

Extracellular signal protein triggering the proteolytic activation of a developmental transcription factor in B. subtilis. Cell (1995) 1.80

Regulation of diaminopimelate decarboxylase synthesis in Escherichia coli. I. Identification of a lysR gene encoding an activator of the lysA gene. J Mol Biol (1983) 1.66

Comment on 'Duplicated sporulation genes in bacteria' by J. Errington, P. Fort and J. Mandelstam. FEBS Lett (1986) 1.62

Identification and characterization of the Bacillus subtilis spoIIP locus. J Bacteriol (1995) 1.46

Localization of the sporulation protein SpoIIE in Bacillus subtilis is dependent upon the cell division protein FtsZ. Mol Microbiol (1997) 1.44

Nucleotide sequence and expression of the Escherichia coli dapB gene. J Biol Chem (1984) 1.44

Molecular cloning, characterization, and chromosomal localization of dapF, the Escherichia coli gene for diaminopimelate epimerase. J Bacteriol (1987) 1.43

Cloning, characterization, and expression of the dapE gene of Escherichia coli. J Bacteriol (1992) 1.42

Nucleotide sequence of the asd gene of Escherichia coli: absence of a typical attenuation signal. EMBO J (1982) 1.38

Multiple regulatory signals in the control region of the Escherichia coli carAB operon. Proc Natl Acad Sci U S A (1984) 1.37

The spoIIN279(ts) mutation affects the FtsA protein of Bacillus subtilis. Biochimie (1992) 1.34

Cloning, characterization, and expression of the spoVB gene of Bacillus subtilis. J Bacteriol (1991) 1.34

Septation, dephosphorylation, and the activation of sigmaF during sporulation in Bacillus subtilis. Genes Dev (1999) 1.30

Identification of the genes in the Escherichia coli ileS-lsp operon. Analysis of multiple polycistronic mRNAs made in vivo. J Biol Chem (1987) 1.30

A gene for a new lipoprotein in the dapA-purC interval of the Escherichia coli chromosome. J Bacteriol (1991) 1.22

The SpoIIE phosphatase, the sporulation septum and the establishment of forespore-specific transcription in Bacillus subtilis: a reassessment. Mol Microbiol (1999) 1.12

Transcription of spoIVB is the only role of sigma G that is essential for pro-sigma K processing during spore formation in Bacillus subtilis. J Bacteriol (1995) 1.00

Binding of the Bacillus subtilis spoIVCA product to the recombination sites of the element interrupting the sigma K-encoding gene. Proc Natl Acad Sci U S A (1992) 0.98

Cell-type specificity during development in Bacillus subtilis: the molecular and morphological requirements for sigma E activation. EMBO J (1995) 0.97

Usefulness of the European Epidemic Intelligence Information System in the management of an outbreak of listeriosis, Belgium, 2011. Euro Surveill (2012) 0.93

Bacillus subtilis locus encoding a killer protein and its antidote. J Bacteriol (2001) 0.92

Identification of a new variable number tandem repeat locus in Mycobacterium ulcerans for potential strain discrimination among African isolates. Clin Microbiol Infect (2007) 0.91

Nucleotide sequence of the lsp-dapB interval in Escherichia coli. Nucleic Acids Res (1991) 0.87

Regulatory pattern of the Escherichia coli lysA gene: expression of chromosomal lysA-lacZ fusions. J Bacteriol (1983) 0.86

[Follow-up of the first case of Mycobacterium ulcerans infection documented by PCR, genotyping and culture in the Republic of Congo-Brazzaville]. Med Trop (Mars) (2008) 0.86

Pseudomonas aeruginosa diaminopimelate decarboxylase: evolutionary relationship with other amino acid decarboxylases. Mol Biol Evol (1988) 0.85

Expression in mammalian cells of the diaminopimelic acid decarboxylase of Escherichia coli permits cell growth in lysine-free medium. Eur J Biochem (1985) 0.79

CNRS defended. Nature (1994) 0.75