Initial transcription by RNA polymerase proceeds through a DNA-scrunching mechanism

被引:317
作者
Kapanidis, Achillefs N. [1 ]
Margeat, Emmanuel
Ho, Sam On
Kortkhonjia, Ekaterine
Weiss, Shimon
Ebright, Richard H.
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Physiol, Los Angeles, CA 90095 USA
[3] Univ Oxford, Dept Phys, Clarendon Lab, Oxford OX1 3PU, England
[4] Univ Oxford, IRC Bionanotechnol, Oxford OX1 3PU, England
[5] Rutgers State Univ, Dept Chem, Howard Hughes Med Inst, Piscataway, NJ 08854 USA
[6] Rutgers State Univ, Waksman Inst, Piscataway, NJ 08854 USA
关键词
D O I
10.1126/science.1131399
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Using fluorescence resonance energy transfer to monitor distances within single molecules of abortively initiating transcription initiation complexes, we show that initial transcription proceeds through a "scrunching'' mechanism, in which RNA polymerase ( RNAP) remains fixed on promoter DNA and pulls downstream DNA into itself and past its active center. We show further that putative alternative mechanisms for RNAP active-center translocation in initial transcription, involving "transient excursions" of RNAP relative to DNA or "inchworming" of RNAP relative to DNA, do not occur. The results support a model in which a stressed intermediate, with DNA-unwinding stress and DNA-compaction stress, is formed during initial transcription, and in which accumulated stress is used to drive breakage of interactions between RNAP and promoter DNA and between RNAP and initiation factors during promoter escape.
引用
收藏
页码:1144 / 1147
页数:4
相关论文
共 29 条