Transcription

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SubtiExpress - A database integrating gene expression of all genes under 104 conditions

Genes in this functional category

RNA polymerase

Sigma factors

  • SigA: housekeeping sigma factor
  • SigB: general stress sigma factor
  • SigD: sigma factor for chemotaxis and motility genes
  • SigE: early mother cell-specific sporulation sigma factor
  • SigF: early forespore-specific sporulation sigma factor
  • SigG: late forespore-specific sporulation sigma factor
  • SigH: sigma factor that controls genes of the transition phase
  • SigI:
  • SigK: late mother cell-specific sporulation sigma factor
  • SigL: enhancer-dependent sigma factor (Sigma-54 family)
  • SigM: ECF sigma factor, controls genes required at high salt concentrations
  • SigV: ECF sigma factor
  • SigW: ECF sigma factor, mediates the transcriptional response to cell wall stress PubMed
  • SigX: ECF sigma factor
  • SigY: ECF sigma factor
  • SigZ: ECF sigma factor
  • Xpf
  • YlaC
  • SigO-RsoA: (composite sigma factor)

Transcription elongation/ termination

Important publications

Vladimir Bidnenko, Pierre Nicolas, Aleksandra Grylak-Mielnicka, Olivier Delumeau, Sandrine Auger, Anne Aucouturier, Cyprien Guerin, Francis Repoila, Jacek Bardowski, Stéphane Aymerich, Elena Bidnenko
Termination factor Rho: From the control of pervasive transcription to cell fate determination in Bacillus subtilis.
PLoS Genet.: 2017, 13(7);e1006909
[PubMed:28723971] [WorldCat.org] [DOI] (I e)

Ivan Junier, Olivier Rivoire
Conserved Units of Co-Expression in Bacterial Genomes: An Evolutionary Insight into Transcriptional Regulation.
PLoS ONE: 2016, 11(5);e0155740
[PubMed:27195891] [WorldCat.org] [DOI] (I e)

Matthew H Larson, Rachel A Mooney, Jason M Peters, Tricia Windgassen, Dhananjaya Nayak, Carol A Gross, Steven M Block, William J Greenleaf, Robert Landick, Jonathan S Weissman
A pause sequence enriched at translation start sites drives transcription dynamics in vivo.
Science: 2014, 344(6187);1042-7
[PubMed:24789973] [WorldCat.org] [DOI] (I p)

Pierre Nicolas, Ulrike Mäder, Etienne Dervyn, Tatiana Rochat, Aurélie Leduc, Nathalie Pigeonneau, Elena Bidnenko, Elodie Marchadier, Mark Hoebeke, Stéphane Aymerich, Dörte Becher, Paola Bisicchia, Eric Botella, Olivier Delumeau, Geoff Doherty, Emma L Denham, Mark J Fogg, Vincent Fromion, Anne Goelzer, Annette Hansen, Elisabeth Härtig, Colin R Harwood, Georg Homuth, Hanne Jarmer, Matthieu Jules, Edda Klipp, Ludovic Le Chat, François Lecointe, Peter Lewis, Wolfram Liebermeister, Anika March, Ruben A T Mars, Priyanka Nannapaneni, David Noone, Susanne Pohl, Bernd Rinn, Frank Rügheimer, Praveen K Sappa, Franck Samson, Marc Schaffer, Benno Schwikowski, Leif Steil, Jörg Stülke, Thomas Wiegert, Kevin M Devine, Anthony J Wilkinson, Jan Maarten van Dijl, Michael Hecker, Uwe Völker, Philippe Bessières, Philippe Noirot
Condition-dependent transcriptome reveals high-level regulatory architecture in Bacillus subtilis.
Science: 2012, 335(6072);1103-6
[PubMed:22383849] [WorldCat.org] [DOI] (I p)

Evert-Jan Blom, Anja N J A Ridder, Andrzej T Lulko, Jos B T M Roerdink, Oscar P Kuipers
Time-resolved transcriptomics and bioinformatic analyses reveal intrinsic stress responses during batch culture of Bacillus subtilis.
PLoS ONE: 2011, 6(11);e27160
[PubMed:22087258] [WorldCat.org] [DOI] (I p)

Houra Merrikh, Cristina Machón, William H Grainger, Alan D Grossman, Panos Soultanas
Co-directional replication-transcription conflicts lead to replication restart.
Nature: 2011, 470(7335);554-7
[PubMed:21350489] [WorldCat.org] [DOI] (I p)


Reviews

Georgiy A Belogurov, Irina Artsimovitch
Regulation of Transcript Elongation.
Annu. Rev. Microbiol.: 2015, 69;49-69
[PubMed:26132790] [WorldCat.org] [DOI] (I p)

Julio A Freyre-González, Alejandra M Manjarrez-Casas, Enrique Merino, Mario Martinez-Nuñez, Ernesto Perez-Rueda, Rosa-María Gutiérrez-Ríos
Lessons from the modular organization of the transcriptional regulatory network of Bacillus subtilis.
BMC Syst Biol: 2013, 7;127
[PubMed:24237659] [WorldCat.org] [DOI] (I e)

Lakshminarayan M Iyer, L Aravind
Insights from the architecture of the bacterial transcription apparatus.
J. Struct. Biol.: 2012, 179(3);299-319
[PubMed:22210308] [WorldCat.org] [DOI] (I p)

Thomas J Santangelo, Irina Artsimovitch
Termination and antitermination: RNA polymerase runs a stop sign.
Nat. Rev. Microbiol.: 2011, 9(5);319-29
[PubMed:21478900] [WorldCat.org] [DOI] (I p)

Evgeny Nudler
RNA polymerase active center: the molecular engine of transcription.
Annu. Rev. Biochem.: 2009, 78;335-61
[PubMed:19489723] [WorldCat.org] [DOI] (I p)

P J Lewis, G P Doherty, J Clarke
Transcription factor dynamics.
Microbiology (Reading, Engl.): 2008, 154(Pt 7);1837-44
[PubMed:18599813] [WorldCat.org] [DOI] (P p)

Tanja M Gruber, Carol A Gross
Multiple sigma subunits and the partitioning of bacterial transcription space.
Annu. Rev. Microbiol.: 2003, 57;441-66
[PubMed:14527287] [WorldCat.org] [DOI] (P p)

Sergei Borukhov, Konstantin Severinov
Role of the RNA polymerase sigma subunit in transcription initiation.
Res. Microbiol.: 2002, 153(9);557-62
[PubMed:12455702] [WorldCat.org] (P p)

Paul Gollnick, Paul Babitzke
Transcription attenuation.
Biochim. Biophys. Acta: 2002, 1577(2);240-50
[PubMed:12213655] [WorldCat.org] (P p)

John D Helmann
The extracytoplasmic function (ECF) sigma factors.
Adv. Microb. Physiol.: 2002, 46;47-110
[PubMed:12073657] [WorldCat.org] (P p)

E Nudler
Transcription elongation: structural basis and mechanisms.
J. Mol. Biol.: 1999, 288(1);1-12
[PubMed:10329121] [WorldCat.org] [DOI] (P p)

W G Haldenwang
The sigma factors of Bacillus subtilis.
Microbiol. Rev.: 1995, 59(1);1-30
[PubMed:7708009] [WorldCat.org] (P p)


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