Pulling on the nascent RNA during transcription does not alter kinetics of elongation or ubiquitous pausing

被引:43
作者
Dalal, Ravindra V.
Larson, Matthew H.
Neuman, Keir C.
Gelles, Jeff
Landick, Robert
Block, Steven M. [1 ]
机构
[1] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Phys, Stanford, CA 94305 USA
[3] Stanford Univ, Biophys Program, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[5] Brandeis Univ, Dept Biochem, Waltham, MA 02454 USA
[6] Univ Wisconsin, Dept Bacteriol, Madison, WI 53706 USA
关键词
D O I
10.1016/j.molcel.2006.06.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcriptional elongation and termination by RNA polymerase (RNAP) are controlled by interactions among the nascent RNA, DNA, and RNAP that comprise the ternary transcription elongation complex (TEC). To probe the effects of cotranscriptionally folded RNA hairpins on elongation as well as the stability of the TEC, we developed a single-molecule assay to monitor RNA elongation by Escherichia coli RNAP molecules while applying controlled loads to the nascent RNA that favor forward translocation. Remarkably, forces up to 30 pN, twice those required to disrupt RNA secondary structure, did not significantly affect enzyme processivity, transcription elongation rates, pause frequencies, or pause lifetimes. These results indicate that ubiquitous transcriptional pausing is not a consequence of the formation of hairpins in the nascent RNA. The ability of the TEC to sustain large loads on the transcript reflects a tight binding of RNA within the TEC and has important implications for models of transcriptional termination.
引用
收藏
页码:231 / 239
页数:9
相关论文
共 44 条
[1]   Direct observation of base-pair stepping by RNA polymerase [J].
Abbondanzieri, EA ;
Greenleaf, WJ ;
Shaevitz, JW ;
Landick, R ;
Block, SM .
NATURE, 2005, 438 (7067) :460-465
[2]   Molecular mechanism of transcription inhibition by peptide antibiotic microcin J25 [J].
Adelman, K ;
Yuzenkova, J ;
La Porta, A ;
Zenkin, N ;
Lee, J ;
Lis, JT ;
Borukhov, S ;
Wang, MD ;
Severinov, K .
MOLECULAR CELL, 2004, 14 (06) :753-762
[3]   Single molecule analysis of RNA polymerase elongation reveals uniform kinetic behavior [J].
Adelman, K ;
La Porta, A ;
Santangelo, TJ ;
Lis, JT ;
Roberts, JW ;
Wang, MD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (21) :13538-13543
[4]   Pausing by bacterial RNA polymerase is mediated by mechanistically distinct classes of signals [J].
Artsimovitch, I ;
Landick, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (13) :7090-7095
[5]   The transcriptional regulator RfaH stimulates RNA chain synthesis after recruitment to elongation complexes by the exposed nontemplate DNA strand [J].
Artsimovitch, I ;
Landick, R .
CELL, 2002, 109 (02) :193-203
[6]   RfaH and the ops element, components of a novel system controlling bacterial transcription elongation [J].
Bailey, MJA ;
Hughes, C ;
Koronakis, V .
MOLECULAR MICROBIOLOGY, 1997, 26 (05) :845-851
[7]   A ratchet mechanism of transcription elongation and its control [J].
Bar-Nahum, G ;
Epshtein, V ;
Ruckenstein, AE ;
Rafikov, R ;
Mustaev, A ;
Nudler, E .
CELL, 2005, 120 (02) :183-193
[8]   DISSECTION OF THE HIS LEADER PAUSE SITE BY BASE SUBSTITUTION REVEALS A MULTIPARTITE SIGNAL THAT INCLUDES A PAUSE RNA HAIRPIN [J].
CHAN, CL ;
LANDICK, R .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 233 (01) :25-42
[9]   Stretching single stranded DNA, a model polyelectrolyte [J].
Dessinges, MN ;
Maier, B ;
Zhang, Y ;
Peliti, M ;
Bensimon, D ;
Croquette, V .
PHYSICAL REVIEW LETTERS, 2002, 89 (24)
[10]   The many conformational states of RNA polymerase elongation complexes and their roles in the regulation of transcription [J].
Erie, DA .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2002, 1577 (02) :224-239