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Mutations upstream from sdaC and malT in Escherichia coli uncover a complex interplay between the cAMP receptor protein and different sigma factors.


ABSTRACT: In Escherichia coli, one of the best understood microorganisms, much can still be learned about the basic interactions between transcription factors and promoters. When a cAMP-deficient cya mutant is supplied with maltose as the main carbon source, mutations develop upstream from the two genes malT and sdaC. Here, we explore the regulation of the two promoters, using fluorescence-based genetic reporters in combination with both spontaneously evolved and systematically engineered cis-acting mutations. We show that in the cya mutant, regulation of malT and sdaC evolves toward cAMP-independence and increased expression in the stationary phase. Furthermore, we show that the location of the cAMP receptor protein (Crp) binding site upstream of malT is important for alternative sigma factor usage. This provides new insights into the architecture of bacterial promoters and the global interplay between Crp and sigma factors in different growth phases.IMPORTANCEThis work provides new general insights into (1) the architecture of bacterial promoters, (2) the importance of the location of Class I Crp-dependent promoters, and (3) the global interplay between Crp and sigma factors in different growth phases.

SUBMITTER: Frendorf PO 

PROVIDER: S-EPMC10882989 | biostudies-literature | 2024 Feb

REPOSITORIES: biostudies-literature

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Mutations upstream from <i>sdaC</i> and <i>malT</i> in <i>Escherichia coli</i> uncover a complex interplay between the cAMP receptor protein and different sigma factors.

Frendorf Pernille Ott PO   Heyde Sophia A H SAH   Nørholm Morten H H MHH  

Journal of bacteriology 20240110 2


In <i>Escherichia coli</i>, one of the best understood microorganisms, much can still be learned about the basic interactions between transcription factors and promoters. When a cAMP-deficient <i>cya</i> mutant is supplied with maltose as the main carbon source, mutations develop upstream from the two genes <i>malT</i> and <i>sdaC</i>. Here, we explore the regulation of the two promoters, using fluorescence-based genetic reporters in combination with both spontaneously evolved and systematically  ...[more]

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