AI Article Synopsis

  • The study analyzes the gene expression regulated by the cyclic AMP receptor protein (Crp), focusing on genes related to central carbon metabolism and how they are influenced by catabolite repression or activation.
  • Key findings indicate that many operons for central carbon metabolic enzymes face direct repression by Crp, while few enzyme genes and an abundance of ribosomal/tRNA genes are activated indirectly by glucose through Crp.
  • The research reinforces the role of Crp in regulating stress response proteins through strong indirect catabolite repression, confirmed through various experimental approaches like real-time PCR and reporter gene assays.

Article Abstract

We report here the transcriptome analyses of highly expressed genes that are subject to catabolite repression or activation mediated by the cyclic AMP receptor protein (Crp). The results reveal that many operons encoding enzymes of central carbon metabolic pathways (e.g., Krebs cycle enzymes), as well as transporters and enzymes that initiate carbon metabolism, are subject to direct Crp-mediated catabolite repression. By contrast, few enzyme-encoding genes (direct regulation) but many ribosomal protein- and tRNA-encoding genes (indirect regulation) are subject to Crp-dependent glucose activation. Additionally, Crp mediates strong indirect catabolite repression of many cytoplasmic stress response proteins, including the major chaperone proteins, five ATP-dependent protease complexes, and several cold and heat shock proteins. These results were confirmed by (i) phenotypic analyses, (ii) real-time PCR studies, (iii) reporter gene fusion assays, and (iv) previously published reports about representative genes. The results serve to define and extend our appreciation of the Crp regulon.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC415760PMC
http://dx.doi.org/10.1128/JB.186.11.3516-3524.2004DOI Listing

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