Single-molecule tracking of mRNA exiting from RNA polymerase II

被引:92
作者
Andrecka, Joanna [1 ,2 ,3 ]
Lewis, Robert [1 ,2 ,3 ]
Brueckner, Florian [1 ,2 ,4 ]
Lehmann, Elisabeth [1 ,2 ,4 ]
Cramer, Patrick [1 ,2 ,4 ]
Michaelis, Jens [1 ,2 ,3 ]
机构
[1] Univ Munich, CiPSM, D-81377 Munich, Germany
[2] Univ Munich, CeNS, D-81377 Munich, Germany
[3] Univ Munich, Dept Chem & Biochem, D-81377 Munich, Germany
[4] Univ Munich, Gene Ctr Munich, D-81377 Munich, Germany
关键词
Pol II; transcription; FRET; triangulation; fluorescence;
D O I
10.1073/pnas.0703815105
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
Single-pair fluorescence resonance energy transfer was used to track RNA exiting from RNA polymerase II (Pol II) in elongation complexes. Measuring the distance between the RNA S' end and three known locations within the elongation complex allows us determine its position by means of triangulation. RNA leaves the polymerase active center cleft via the previously proposed exit tunnel and then disengages from the enzyme surface. When the RNA reaches lengths of 26 and 29 nt, its 5' end associates with Pol 11 at the base of the dock domain. Because the initiation factor TFIIB binds to the dock domain and exit tunnel, exiting RNA may prevent TFIIB reassociation during elongation. RNA further extends toward the linker connecting to the polymerase C-terminal repeat domain (CTD), which binds the 5'-capping enzyme and other RNA processing factors.
引用
收藏
页码:135 / 140
页数:6
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