|
|
||||||||
J. Biol. Chem., Vol. 268, Issue 32, 23812-23817, 11, 1993
GB Koudelka and CY Lam
The developmental decisions of bacteriophage 434 depend on the ability of
434 repressor and Cro to bind OR1 and OR3 with different relative
affinities; repressor binds OR1 tighter than OR3, whereas Cro slightly
prefers OR3 over OR1. Studies with operator mutants show that repressor's
lower relative affinity for OR3 results from a deviation in the sequence of
OR3 from consensus; an A-->G change at position 4 in one half-site (OR1:
A-C-A-A-A-C-T-T-T-C-T-T-G-T; OR3: A-C-A-G-T-T-T-T-T- C-T-T-G-T). Similar
experiments show that Cro binds operators containing either A.T or G.C
bases pairs at position 4 equally well, but cannot bind operators
containing C.G or T.A base pairs at this position. A Gln33-->Ala
mutation in 434 repressor diminishes, but does not eliminate, its ability
to distinguish between purines at position 4. This shows that a glutamine
at amino acid 33 is not the sole determinant of repressor's position 4
specificity. Changing Gln33-- >Leu, the amino acid at the homologous
position in Cro, does not confer "Cro-like" position 4 base specificity on
repressor. Similarly, a Cro protein bearing Gln at this position does not
exhibit repressor's position 4 base preferences. The residual specificities
of these mutant proteins indicates that in each protein, more than 1 amino
acid is responsible for recognizing bases at position 4. These were
identified by analyzing the binding specificities of multiply mutated
repressors, in vitro. The types of substitutions made were guided by
sequence homologies between 434 repressor and Cro. At least three mutations
are needed to eliminate repressor's position 4 base specificity; Gln33--
>Ala, Glu32-->Gln, and Thr27-->Lys, although no set of amino acid
substitutions in repressor was able to confer Cro-like position 4
specificity to repressor. These results indicate that at least the amino
acids at these positions are involved in recognition of the position 4
base. Other evidence suggests that Cro and repressor use identical amino
acids present at homologous positions in the DNA recognition helix in
different ways.
Differential recognition of OR1 and OR3 by bacteriophage 434 repressor and Cro
Department of Biological Sciences, State University of New York at Buffalo 14260.
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
G. Durante-Rodriguez, M. T. Zamarro, J. L. Garcia, E. Diaz, and M. Carmona New insights into the BzdR-mediated transcriptional regulation of the anaerobic catabolism of benzoate in Azoarcus sp. CIB Microbiology, January 1, 2008; 154(1): 306 - 316. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. van Dijk, A. D. J. van Dijk, V. Hsu, R. Boelens, and A. M. J. J. Bonvin Information-driven protein-DNA docking using HADDOCK: it is a matter of flexibility Nucleic Acids Res., July 4, 2006; 34(11): 3317 - 3325. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. L. Barragan, B. Blazquez, M. T. Zamarro, J. M. Mancheno, J. L. Garcia, E. Diaz, and M. Carmona BzdR, a Repressor That Controls the Anaerobic Catabolism of Benzoate in Azoarcus sp. CIB, Is the First Member of a New Subfamily of Transcriptional Regulators J. Biol. Chem., March 18, 2005; 280(11): 10683 - 10694. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Fromknecht, P. D. Vogel, and J. G. Wise Combinatorial Redesign of the DNA Binding Specificity of a Prokaryotic Helix-Turn-Helix Repressor J. Bacteriol., January 15, 2003; 185(2): 475 - 481. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Xu and G. B. Koudelka DNA-based Positive Control Mutants in the Binding Site Sequence of 434 Repressor J. Biol. Chem., September 11, 1998; 273(37): 24165 - 24172. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. C. Bell and G. B. Koudelka How 434 Repressor Discriminates Between O(R)1 and O(R)3 J. Biol. Chem., January 20, 1995; 270(3): 1205 - 1212. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Molecular and Cellular Proteomics |
| Journal of Lipid Research | ASBMB Today |