Insights into the Quality of DnaA Boxes and Their Cooperativity
Plasmids carrying the mioC promoter region with its two DnaA boxes are as efficient in titration of DnaA protein as plasmids carrying a replication-inactivated oriC region with its five DnaA boxes. The two DnaA boxes upstream of the mioC promoter were mutated in various ways to study the cooperativi...
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Veröffentlicht in: | Journal of molecular biology 2006-01, Vol.355 (1), p.85-95 |
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Sprache: | eng |
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Zusammenfassung: | Plasmids carrying the
mioC promoter region with its two DnaA boxes are as efficient in titration of DnaA protein as plasmids carrying a replication-inactivated
oriC region with its five DnaA boxes. The two DnaA boxes upstream of the
mioC promoter were mutated in various ways to study the cooperativity between the DnaA boxes, and to study
in vivo the
in vitro-defined 9mer DnaA box consensus sequence (TT
A/
TTNCACA). The quality and cooperativity of the DnaA boxes were determined in two complementary ways: as titration of DnaA protein leading to derepression of the
dnaA promoter, and as repression of the
mioC promoter caused by the DnaA protein binding to the DnaA boxes. Titration of DnaA protein correlated with repression of the
mioC promoter. The level of titration and repression with the normal promoter-proximal box (TTTTCCACA) depends strongly on the presence and the quality of a DnaA box in the promoter-distal position, whereas a promoter-proximal DnaA box with the sequence TTATCCACA titrated DnaA protein and caused significant repression of the
mioC promoter without a promoter-distal DnaA box. The quality of the eight different consensus DnaA boxes located in the promoter-proximal position was determined: TTATCCACA had the highest affinity for DnaA protein. In the third position, A was better than T, and the four possibilities in the fifth position could be ranked as C >A ≥G >T. Parallel
in vitro experiments using a purified DNA-binding domain of DnaA protein gave the same ranking of the binding affinities of the eight DnaA boxes. |
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ISSN: | 0022-2836 1089-8638 |
DOI: | 10.1016/j.jmb.2005.10.036 |