|
Originally published In Press as doi:10.1074/jbc.M112481200 on February 19, 2002
J. Biol. Chem., Vol. 277, Issue 18, 15407-15412, May 3, 2002
Generality of the Branched Pathway in Transcription Initiation by
Escherichia coli RNA Polymerase*
Motoki
Susa §,
Ranjan
Sen ¶, and
Nobuo
Shimamoto §
From the Structural Biology Center, National
Institute of Genetics, and the § Department of
Genetics, School of Life Science, The Graduate University for
Advanced Studies, 1111 Yata, Mishima, Japan, 411-8540
Transcription initiation has been assumed to be a
multi-step sequential process, although additional steps could exist.
Initiation from the T7A1 promoter, in particular, apparently behaves
in vitro in a manner that can be fully explained by the
sequential pathway. However, initiation from the
PRAL promoter has been shown to follow a
branched pathway from which a part of the enzyme-promoter complex is
arrested at the promoter raising the question as to which mechanism is
general. We found that a moribund complex, characteristic of the
arrested branch, is formed at the T7A1 promoter, especially in low salt
condition indicating that the initiation mechanism for this promoter is
also branched. The results of DNA footprinting suggested that
holoenzyme in the moribund complex is dislocated on DNA from the
position of productive complex. However, only a small fraction of the
binary complex becomes arrested at this promoter, and the
interconversion between subspecies of binary complex is apparently more
reversible than at the PRAL promoter, which
explains why the reaction pathway appears to be sequential. These
findings suggest a generality of the branched pathway mechanism, which
would resolve contradictory observations that have been reported for
various promoters.
*
This work was supported in part by grants from Ministry of
Education (to N. S.) and an Itoh scholarship (to M. S.).The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
¶
Present address: Center for DNA Fingerprinting and
Diagnostics, ECIL Road, Nacharam, Hyderabad 500076, India.
To whom correspondence should be addressed. Tel.:
81-559-81-6843; Fax: 81-559-81-6844; E-mail:
nshima@LAB.nig.ac.jp.
Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
A. Rogozina, E. Zaychikov, M. Buckle, H. Heumann, and B. Sclavi
DNA melting by RNA polymerase at the T7A1 promoter precedes the rate-limiting step at 37{degrees}C and results in the accumulation of an off-pathway intermediate
Nucleic Acids Res.,
July 3, 2009;
(2009)
gkp560v1.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Q. Wang, T. D. Tullius, and J. R. Levin
Effects of Discontinuities in the DNA Template on Abortive Initiation and Promoter Escape by Escherichia coli RNA Polymerase
J. Biol. Chem.,
September 14, 2007;
282(37):
26917 - 26927.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
K. Hosoda, T. Matsuura, H. Kita, N. Ichihashi, K. Tsukada, and T. Yomo
Kinetic Analysis of the Entire RNA Amplification Process by Qbeta Replicase
J. Biol. Chem.,
May 25, 2007;
282(21):
15516 - 15527.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. V. Sukhodolets, S. Garges, and S. Adhya
Ribosomal protein S1 promotes transcriptional cycling
RNA,
August 1, 2006;
12(8):
1505 - 1513.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. A. Mooney and R. Landick
Tethering {sigma}70 to RNA polymerase reveals high in vivo activity of {sigma} factors and {sigma}70-dependent pausing at promoter-distal locations
Genes & Dev.,
November 15, 2003;
17(22):
2839 - 2851.
[Abstract]
[Full Text]
[PDF]
|
 |
|
Copyright © 2002 by the American Society for Biochemistry and Molecular Biology.
|
Advertisement
Advertisement
|