Sequence-dependent kinetic model for transcription elongation by RNA polymerase
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作者:
Bai, L
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Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USACornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
Bai, L
[1
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Shundrovsky, A
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Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USACornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
Shundrovsky, A
[1
]
Wang, MD
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Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USACornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
Wang, MD
[1
]
机构:
[1] Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
We present a kinetic model for the sequence-dependent motion of RNA polymerase (RNAP) during transcription elongation. For each NTP incorporation, RNAP has a net forward translocation of one base-pair along the DNA template. However, this process may involve the exploration of back-tracked and forward-tracked translocation modes. In our model, the kinetic rates for the reaction pathway, calculated based on the stabilities of the transcription elongation complex (TEC), necessarily lead to sequence-dependent NTP incorporation rates. Simulated RNAP elongation kinetics is in good agreement with data from transcription gels and single-molecule studies. The model provides a kinetic explanation for well-known back-tracked pauses at transcript positions with unstable TECs. It also predicts a new type of pause caused by an energetically unfavorable transition from pre to post-translocation modes. (C) 2004 Elsevier Ltd. All rights reserved.