A mathematical model for transcriptional interference by RNA polymerase traffic in Escherichia coli

被引:78
作者
Sneppen, K
Dodd, IB
Shearwin, KE
Palmer, AC
Schubert, RA
Callen, BP
Egan, JB
机构
[1] NORDITA, Nord Inst Theoret Phys, Niels Bohr Inst, DK-2100 Copenhagen, Denmark
[2] Univ Adelaide, Sch Mol & Biomed Sci, Discipline Biochem, Adelaide, SA 5005, Australia
关键词
transcriptional interference; RNA polymerase; occlusion; sitting duck; collision;
D O I
10.1016/j.jmb.2004.11.075
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interactions between RNA polymerases (RNAP) resulting from tandem or convergent arrangements of promoters can cause transcriptional interference, often with important consequences for gene expression. However, it is not known what factors determine the magnitude of interference and which mechanisms are likely to predominate in any situation. We therefore developed a mathematical model incorporating three mechanisms of transcriptional interference in bacteria: occlusion (in which passing RNAPs block access to the promoter), collisions between elongating RNAPs, and "sitting duck" interference (in which RNAP complexes waiting to fire at the promoter are removed by passing RNAP). The predictions of the model are in good agreement with a recent quantitative in vivo study of convergent promoters in E. coli. Our analysis predicts that strong occlusion requires the interfering promoter to be very strong. Collisions can also produce strong interference but only if the interfering promoter is very strong or if the convergent promoters are far apart (> 200 bp). For moderate strength interfering promoters and short inter-promoter distances, strong interference is dependent on the sitting duck mechanism. Sitting duck interference is dependent on the relative strengths of the two promoters. However, it is also dependent on the "aspect ratio" (the relative rates of RNAP binding and firing) of the sensitive promoter, allowing promoters of equal strength to have very different sensitivities to transcriptional interference. The model provides a framework for using transcriptional interference to investigate various dynamic processes on DNA in vivo. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:399 / 409
页数:11
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