Format

Send to

Choose Destination
See comment in PubMed Commons below
J R Soc Interface. 2013 Jun 26;10(86):20130438. doi: 10.1098/rsif.2013.0438. Print 2013 Sep 6.

A rule-based kinetic model of RNA polymerase II C-terminal domain phosphorylation.

Author information

  • 1MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh EH4 2XU, UK. s.aitken@ed.ac.uk

Abstract

The complexity of many RNA processing pathways is such that a conventional systems modelling approach is inadequate to represent all the molecular species involved. We demonstrate that rule-based modelling permits a detailed model of a complex RNA signalling pathway to be defined. Phosphorylation of the RNA polymerase II (RNAPII) C-terminal domain (CTD; a flexible tail-like extension of the largest subunit) couples pre-messenger RNA capping, splicing and 3' end maturation to transcriptional elongation and termination, and plays a central role in integrating these processes. The phosphorylation states of the serine residues of many heptapeptide repeats of the CTD alter along the coding region of genes as a function of distance from the promoter. From a mechanistic perspective, both the changes in phosphorylation and the location at which they take place on the genes are a function of the time spent by RNAPII in elongation as this interval provides the opportunity for the kinases and phosphatases to interact with the CTD. On this basis, we synthesize the available data to create a kinetic model of the action of the known kinases and phosphatases to resolve the phosphorylation pathways and their kinetics.

KEYWORDS:

Kappa; rule-based modelling; transcription

[PubMed - indexed for MEDLINE]
Free PMC Article
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for HighWire Icon for PubMed Central
    Loading ...
    Write to the Help Desk