Direct observation of DNA rotation during transcription by Escherichia coli RNA polymerase
Yoshie Harada (),
Osamu Ohara,
Akira Takatsuki,
Hiroyasu Itoh,
Nobuo Shimamoto and
Kazuhiko Kinosita
Additional contact information
Yoshie Harada: Faculty of Science and Technology, Keio University
Osamu Ohara: Kazusa DNA Research Institute
Akira Takatsuki: Faculty of Science and Technology, Keio University
Hiroyasu Itoh: CREST (Core Research for Evolutional Science and Technology) “Genetic Programming” Team 13
Nobuo Shimamoto: Structural Biology Center, National Institute of Genetics
Kazuhiko Kinosita: Faculty of Science and Technology, Keio University
Nature, 2001, vol. 409, issue 6816, 113-115
Abstract:
Abstract Helical filaments driven by linear molecular motors are anticipated to rotate around their axis, but rotation consistent with the helical pitch has not been observed. 14S dynein1 and non-claret disjunctional protein (ncd)2 rotated a microtubule more efficiently than expected for its helical pitch, and myosin rotated an actin filament only poorly3. For DNA-based motors such as RNA polymerase, transcription-induced supercoiling of DNA4 supports the general picture of tracking along the DNA helix5. Here we report direct and real-time optical microscopy measurements of rotation rate that are consistent with high-fidelity tracking. Single RNA polymerase molecules attached to a glass surface rotated DNA for >100 revolutions around the right-handed screw axis of the double helix with a rotary torque of >5 pN nm. This real-time observation of rotation opens the possibility of resolving individual transcription steps.
Date: 2001
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Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:409:y:2001:i:6816:d:10.1038_35051126
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DOI: 10.1038/35051126
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