scholarly journals Cap analysis gene expression for high-throughput analysis of transcriptional starting point and identification of promoter usage

2003 ◽  
Vol 100 (26) ◽  
pp. 15776-15781 ◽  
Author(s):  
T. Shiraki ◽  
S. Kondo ◽  
S. Katayama ◽  
K. Waki ◽  
T. Kasukawa ◽  
...  
BMC Genetics ◽  
2010 ◽  
Vol 11 (1) ◽  
pp. 25 ◽  
Author(s):  
Caroline Daelemans ◽  
Matthew E Ritchie ◽  
Guillaume Smits ◽  
Sayeda Abu-Amero ◽  
Ian M Sudbery ◽  
...  

2006 ◽  
Vol 86 (3) ◽  
pp. 314-321 ◽  
Author(s):  
Dun Zhou ◽  
Rajneesh Srivastava ◽  
Verena Grummel ◽  
Sabine Cepok ◽  
Hans-Peter Hartung ◽  
...  

2011 ◽  
Vol 154 (1) ◽  
pp. 68-75 ◽  
Author(s):  
K.M. Bourzac ◽  
M.P. Rounseville ◽  
X. Zarate ◽  
V.S.R.K. Maddula ◽  
D.C. Henderson ◽  
...  

Microbiology ◽  
2010 ◽  
Vol 156 (6) ◽  
pp. 1600-1608 ◽  
Author(s):  
Eric Botella ◽  
Mark Fogg ◽  
Matthieu Jules ◽  
Sjouke Piersma ◽  
Geoff Doherty ◽  
...  

Plasmid pBaSysBioII was constructed for high-throughput analysis of gene expression in Bacillus subtilis. It is an integrative plasmid with a ligation-independent cloning (LIC) site, allowing the generation of transcriptional gfpmut3 fusions with desired promoters. Integration is by a Campbell-type event and is non-mutagenic, placing the fusion at the homologous chromosomal locus. Using phoA, murAA, gapB, ptsG and cggR promoters that are responsive to phosphate availability, growth rate and carbon source, we show that detailed profiles of promoter activity can be established, with responses to changing conditions being measurable within 1 min of the stimulus. This makes pBaSysBioII a highly versatile tool for real-time gene expression analysis in growing cells of B. subtilis.


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