The DNA loop model for ara repression: AraC protein occupies the proposed loop sites in vivo and repression-negative mutations lie in these same sites.
AUTOR(ES)
Martin, K
RESUMO
Two sets of experiments have been performed to test the DNA loop model of repression of the araBAD operon of Escherichia coli. First, dimethyl sulfate methylation protection measurements on normally growing cells show that the AraC regulatory protein occupies the araI site in the presence and absence of the inducer arabinose. Similarly, the araO2 site is shown to be occupied by AraC protein in the presence and absence of arabinose; however, its occupancy by AraC is greatly reduced when araI and adjacent sequences are deleted. Thus, AraC protein binds to araO2 cooperatively with some other component of the ara system located at least 60 base pairs away. Second, the mutational analysis presented here shows that the DNA components required for repression of araBAD are araI, araO2, and perhaps the araBAD operon RNA polymerase binding site.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=323581Documentos Relacionados
- Three binding sites for AraC protein are required for autoregulation of araC in Escherichia coli.
- In vivo titration of araC protein.
- Mutations in the araC regulatory gene of Escherichia coli B/r that affect repressor and activator functions of AraC protein.
- Effect of mutations in the cyclic AMP receptor protein-binding site on araBAD and araC expression.
- Novel activation of araC expression and a DNA site required for araC autoregulation in Escherichia coli B/r.