Faculty Opinions recommendation of Structural organization of bacterial RNA polymerase holoenzyme and the RNA polymerase-promoter open complex.

Author(s):  
Robert Dutnall
Cell ◽  
2002 ◽  
Vol 108 (5) ◽  
pp. 599-614 ◽  
Author(s):  
Vladimir Mekler ◽  
Ekaterine Kortkhonjia ◽  
Jayanta Mukhopadhyay ◽  
Jennifer Knight ◽  
Andrei Revyakin ◽  
...  

Author(s):  
Daria Lavysh ◽  
Vladimir Mekler ◽  
Evgeny Klimuk ◽  
Konstantin Severinov

Salmonella enterica serovar Newport bacteriophage 7-11 shares 41 homologous ORFs with Escherichia coli phage phiEco32 and both phages encode a protein similar to bacterial RNA polymerase promoter specificity  subunit. Here, we investigated the temporal pattern of 7-11 gene expression during the infection and compared it to the previously determined transcription strategy of phiEco32. Using primer extension and in vitro transcription assays we identified eight promoters recognized by host RNA polymerase holoenzyme containing 7-11  subunit SaPh711_gp47. These promoters are characterized by a bipartite consensus GTAAtg-(16)-aCTA and are located upstream of late phage genes. While dissimilar from single-element middle and late promoters of phiEco32 recognized by holoenzyme formed by the phi32_gp36  factor, the 7-11 late promoters are located at genome positions similar to those of phiEco32 middle and late promoters. Two early 7-11 promoters are recognized by RNA polymerase holoenzyme containing host primary σ70 factor. Unlike the case of phiEco32, no shut off of σ70-dependent transcription is observed during 7-11 infection and there are no middle promoters. These differences can be explained by the fact that phage 7-11 does not encode a homologue of phi32_gp79, an inhibitor of host and early phage transcription and an activator of transcription by the phi32_gp36-holoenzyme.


2010 ◽  
Vol 75 (3) ◽  
pp. 607-622 ◽  
Author(s):  
Pukhrambam Grihanjali Devi ◽  
Elizabeth A. Campbell ◽  
Seth A. Darst ◽  
Bryce E. Nickels

2006 ◽  
Vol 73 ◽  
pp. 1-10 ◽  
Author(s):  
Nora S. Miroslavova ◽  
Stephen J.W. Busby

Bacterial RNA polymerase holoenzyme carries different determinants that contact different promoter DNA sequence elements. These contacts are essential for the recognition of promoters prior to transcript initiation. Here, we have investigated how active promoters can be built from different combinations of elements. Our results show that the contribution of different contacts to promoter activity is critically dependent on the overall promoter context, and that certain combinations of contacts can hinder transcription initiation.


2021 ◽  
Vol 8 ◽  
Author(s):  
Virtu Solano-Collado ◽  
Sofía Ruiz-Cruz ◽  
Fabián Lorenzo-Díaz ◽  
Radoslaw Pluta ◽  
Manuel Espinosa ◽  
...  

Promoter recognition by RNA polymerase is a key step in the regulation of gene expression. The bacterial RNA polymerase core enzyme is a complex of five subunits that interacts transitory with one of a set of sigma factors forming the RNA polymerase holoenzyme. The sigma factor confers promoter specificity to the RNA polymerase. In the Gram-positive pathogenic bacterium Streptococcus pneumoniae, most promoters are likely recognized by SigA, a poorly studied housekeeping sigma factor. Here we present a sequence conservation analysis and show that SigA has similar protein architecture to Escherichia coli and Bacillus subtilis homologs, namely the poorly conserved N-terminal 100 residues and well-conserved rest of the protein (domains 2, 3, and 4). Further, we have purified the native (untagged) SigA protein encoded by the pneumococcal R6 strain and reconstituted an RNA polymerase holoenzyme composed of the E. coli core enzyme and the sigma factor SigA (RNAP-SigA). By in vitro transcription, we have found that RNAP-SigA was able to recognize particular promoters, not only from the pneumococcal chromosome but also from the S. agalactiae promiscuous antibiotic-resistance plasmid pMV158. Specifically, SigA was able to direct the RNA polymerase to transcribe genes involved in replication and conjugative mobilization of plasmid pMV158. Our results point to the versatility of SigA in promoter recognition and its contribution to the promiscuity of plasmid pMV158.


2002 ◽  
Vol 9 (3) ◽  
pp. 527-539 ◽  
Author(s):  
Elizabeth A. Campbell ◽  
Oriana Muzzin ◽  
Mark Chlenov ◽  
Jing L. Sun ◽  
C.Anders Olson ◽  
...  

Author(s):  
D. G. Vassylyev ◽  
S. Sekine ◽  
O. Laptenko ◽  
J. Lee ◽  
M. N. Vassylyeva ◽  
...  

2015 ◽  
Author(s):  
Brian Bae ◽  
Andrey Feklistov ◽  
Agnieszka Lass-Napiorkowska ◽  
Robert Landick ◽  
Seth A Darst

2014 ◽  
Vol 289 (35) ◽  
pp. 24549-24559 ◽  
Author(s):  
Ritwika S. Basu ◽  
Brittany A. Warner ◽  
Vadim Molodtsov ◽  
Danil Pupov ◽  
Daria Esyunina ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document