scholarly journals Integrated genome-wide analysis of transcription factor occupancy, RNA polymerase II binding and steady-state RNA levels identify differentially regulated functional gene classes

2011 ◽  
Vol 40 (1) ◽  
pp. 148-158 ◽  
Author(s):  
Michal Mokry ◽  
Pantelis Hatzis ◽  
Jurian Schuijers ◽  
Nico Lansu ◽  
Frans-Paul Ruzius ◽  
...  
2013 ◽  
Vol 9 (1) ◽  
pp. 638 ◽  
Author(s):  
Astrid Eijkelenboom ◽  
Michal Mokry ◽  
Elzo de Wit ◽  
Lydia M Smits ◽  
Paulien E Polderman ◽  
...  

Genomics Data ◽  
2016 ◽  
Vol 7 ◽  
pp. 250-255 ◽  
Author(s):  
Ryan P. McNamara ◽  
Carlos Guzman ◽  
Jonathan E. Reeder ◽  
Iván D'Orso

BMC Genomics ◽  
2014 ◽  
Vol 15 (1) ◽  
pp. 959 ◽  
Author(s):  
Ragini Rai ◽  
Lei Zhu ◽  
Haifen Chen ◽  
Archana Gupta ◽  
Siu Sze ◽  
...  

2017 ◽  
Vol 66 (1) ◽  
pp. 38-49.e6 ◽  
Author(s):  
Carlo Baejen ◽  
Jessica Andreani ◽  
Phillipp Torkler ◽  
Sofia Battaglia ◽  
Bjoern Schwalb ◽  
...  

Genetics ◽  
1996 ◽  
Vol 142 (3) ◽  
pp. 737-747 ◽  
Author(s):  
Jacques Archambault ◽  
David B Jansma ◽  
James D Friesen

Abstract In the yeast Saccharomyces cerevisiae, mutations in genes encoding subunits of RNA polymerase II (RNAPII) often give rise to a set of pleiotropic phenotypes that includes temperature sensitivity, slow growth and inositol auxotrophy. In this study, we show that these phenotypes can be brought about by a reduction in the intracellular concentration of RNAPII. Underproduction of RNAPII was achieved by expressing the gene (RPO21), encoding the largest subunit of the enzyme, from the LEU2 promoter or a weaker derivative of it, two promoters that can be repressed by the addition of leucine to the growth medium. We found that cells that underproduced RPO21 were unable to derepress fully the expression of a reporter gene under the control of the INO1 UAS. Our results indicate that temperature sensitivity, slow growth and inositol auxotrophy is a set of phenotypes that can be caused by lowering the steady-state amount of RNAPII; these results also lead to the prediction that some of the previously identified RNAPII mutations that confer this same set of phenotypes affect the assembly/stability of the enzyme. We propose a model to explain the hypersensitivity of INO1 transcription to mutations that affect components of the RNAPII transcriptional machinery.


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