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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 250 (1996), S. 742-749 
    ISSN: 1617-4623
    Keywords: Key words AbrB ; DNA binding ; Global regulation ; Sporulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  AbrB is a global transcriptional regulator of many genes that are expressed as Bacillus subtilis exits from active growth into stationary phase and sporulation. Previous results have suggested that binding of AbrB at some promoters involves multiple sites of recognition and is a cooperative process. It is shown here that the binding site at spo0E can be subdivided into 5′ and 3′ halves, each capable of directing AbrB binding. In addition, the central portion of the intact site can promote AbrB binding. Examination of various heterologous and homologous tandem combinations of the half-sites confirms that the native site is a complex array of overlapping suboptimal sites, the precise arrangement of which is required for optimal AbrB binding. Other data suggest that binding of multiple AbrB units is needed for stable complex formation. A binding mechanism involving numerous steps of intermediate affinity is envisioned.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 250 (1996), S. 742-749 
    ISSN: 1617-4623
    Keywords: AbrB ; DNA binding ; Global regulation ; Sporulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract AbrB is a global transcriptional regulator of many genes that are expressed asBacillus subtilis exits from active growth into stationary phase and sporulation. Previous results have suggested that binding of AbrB at some promoters involves multiple sites of recognition and is a cooperative process. It is shown here that the binding site atspo0E can be subdivided into 5′ and 3′ halves, each capable of directing AbrB binding. In addition, the central portion of the intact site can promote AbrB binding. Examination of various heterologous and homologous tandem combinations of the half-sites confirms that the native site is a complex array of overlapping suboptimal sites, the precise arrangement of which is required for optimal AbrB binding. Other data suggest that binding of multiple AbrB units is needed for stable complex formation. A binding mechanism involving numerous steps of intermediate affinity is envisioned.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
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