Model-driven experimental design workflow expands understanding of regulatory role of Nac in Escherichia coli. Issue 1 (20th January 2023)

• Record Type: Journal Article
• Authors: Park, Joon Young; Lee, Sang-Mok; Ebrahim, Ali; Scott-Nevros, Zoe K; Kim, Jaehyung; Yang, Laurence; Sastry, Anand; Seo, Sang Woo; Palsson, Bernhard O; Kim, Donghyuk
• Is Part Of: NAR genomics and bioinformatics. Volume 5:Issue 1(2023)
• Publication Date: 2023-01-20
• Subjects: Genomics -- Periodicals; Bioinformatics -- Periodicals; 572.8
• DOI: 10.1093/nargab/lqad006
• Languages: English
• ISSNs: 2631-9268

Abstract

Abstract: The establishment of experimental conditions for transcriptional regulator network (TRN) reconstruction in bacteria continues to be impeded by the limited knowledge of activating conditions for transcription factors (TFs). Here, we present a novel genome-scale model-driven workflow for designing experimental conditions, which optimally activate specific TFs. Our model-driven workflow was applied to elucidate transcriptional regulation under nitrogen limitation by Nac and NtrC, in Escherichia coli . We comprehensively predict alternative nitrogen sources, including cytosine and cytidine, which trigger differential activation of Nac using a model-driven workflow. In accordance with the prediction, genome-wide measurements with ChIP-exo and RNA-seq were performed. Integrative data analysis reveals that the Nac and NtrC regulons consist of 97 and 43 genes under alternative nitrogen conditions, respectively. Functional analysis of Nac at the transcriptional level showed that Nac directly down-regulates amino acid biosynthesis and restores expression of tricarboxylic acid (TCA) cycle genes to alleviate nitrogen-limiting stress. We also demonstrate that both TFs coherently modulate α-ketoglutarate accumulation stress due to nitrogen limitation by co-activating amino acid and diamine degradation pathways. A systems-biology approach provided a detailed and quantitative understanding of both TF's roles and how nitrogen and carbon metabolic networks respond complementarily to nitrogen-limiting stress.