Single molecule analysis of RNA polymerase elongation reveals uniform kinetic behavior
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作者:
Adelman, K
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机构:Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
Adelman, K
La Porta, A
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机构:Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
La Porta, A
Santangelo, TJ
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机构:Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
Santangelo, TJ
Lis, JT
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机构:Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
Lis, JT
Roberts, JW
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机构:Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
Roberts, JW
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
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机构:
[1] Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
By using single-molecule measurements, we demonstrate that the elongation kinetics of individual Escherichia coli RNA polymerase molecules are remarkably homogeneous. We find no evidence of distinct elongation states among RNA polymerases. Instead, the observed heterogeneity in transcription rates results from statistical variation in the frequency and duration of pausing. When transcribing a gene without strong pause sites, RNA polymerase molecules display transient pauses that are distributed randomly in both time and distance. Transitions between the active elongation mode and the paused state are instantaneous within the resolution of our measurements (<1 s). This elongation behavior is compared with that of a mutant RNA polymerase that pauses more frequently and elongates more slowly than wild type.