SNU CBE

Systems assessment of transcriptional regulation on central carbon metabolism by Cra and CRP

2018 · Nucleic Acids Research

저자

Donghyuk Kim, 서상우 (Sang Woo Seo), Ye Gao, Hojung Nam, Gabriela I. Guzmán, Byung‐Kwan Cho, Bernhard Ørn Palsson

연구주제

Microbial Metabolic Engineering and Bioproduction · Bacterial Genetics and Biotechnology

NTIS 과학기술표준분류

가장 가까운 분류(생명과학 > 융합바이오 > 시스템생물학)가 화학·화공 범위 밖이다. 배정 근거: AI 키워드가 잡은 NTIS 과제의 분류.

AI 연구 키워드·방법

catabolite repression central carbon metabolism 유전체 규모 대사 모델(GEM) 전사조절 네트워크

chip exo sequencing RNA 시퀀싱(RNA-seq)

키워드 (OpenAlex)

catabolite repression central carbon metabolism Escherichia coli transcriptional regulation DNA binding sites glyoxylate cycle respiratory pathways genome-scale metabolic models

초록

Two major transcriptional regulators of carbon metabolism in bacteria are Cra and CRP. CRP is considered to be the main mediator of catabolite repression. Unlike for CRP, in vivo DNA binding information of Cra is scarce. Here we generate and integrate ChIP-exo and RNA-seq data to identify 39 binding sites for Cra and 97 regulon genes that are regulated by Cra in Escherichia coli. An integrated metabolic-regulatory network was formed by including experimentally-derived regulatory information and a genome-scale metabolic network reconstruction. Applying analysis methods of systems biology to this integrated network showed that Cra enables optimal bacterial growth on poor carbon sources by redirecting and repressing glycolysis flux, by activating the glyoxylate shunt pathway, and by activating the respiratory pathway. In these regulatory mechanisms, the overriding regulatory activity of Cra…

이 논문을 지원한 국가R&D 과제 (NTIS 성과)

NTIS 성과DB(2020–24)에서 DOI 매칭 없음

인접 그래프

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교수 1

서상우

연구주제 1

Microbial Metabolic Engineering and Bioproduction

키워드 2

전사조절 네트워크 · 유전체 규모 대사 모델(GEM)

방법 1

RNA 시퀀싱(RNA-seq)