Abstract

Cyanobacteria dynamically relay environmental inputs to intracellular adaptations through a coordinated adjustment of photosynthetic efficiency and carbon processing rates. The output of such adaptations is reflected through changes in transcriptional patterns and metabolic flux distributions that ultimately define growth strategy. To address interrelationships between metabolism and regulation, we performed integrative analyses of metabolic and gene co-expression networks in a model cyanobacterium, Synechococcus sp. PCC 7002. Centrality analyses using the gene co-expression network identified a set of key genes, which were defined here as “topologically important.” Parallel in silico gene knock-out simulations, using the genome-scale metabolic network, classified what we termed as “functionally important” genes, deletion of which affected growth or metabolism. A strong positive correlation was observed between topologically and functionally important genes. Functionally important genes exhibited variable levels of topological centrality; however, the majority of topologically central genes were found to be functionally essential for growth. Subsequent functional enrichment analysis revealed that both functionally and topologically important genes in Synechococcus sp. PCC 7002 are predominantly associated with translation and energy metabolism, two cellular processes critical for growth. This research demonstrates how synergistic network-level analyses can be used for reconciliation of metabolic and gene expression data to uncover fundamental biological principles.

Highlights

  • The regulatory machinery of cyanobacteria, which evolved to provide ecophysiological advantages across a dynamic range of conditions, plays a major role in both short- and long-term adaptations

  • Degree distributions of both networks appear as straight lines on log-log plots (Supplementary Figure S1a,b), implying that the developed coexpression networks of Synechococcus 7002 are robust and scale-free

  • The number of nodes of the first and second largest components of GCN1 (GCN2) was 985 (52) and 34 (10), respectively with all of the topologically central genes identified in our analysis clustering into the first largest components

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Summary

Introduction

The regulatory machinery of cyanobacteria, which evolved to provide ecophysiological advantages across a dynamic range of conditions, plays a major role in both short- and long-term adaptations. To identify the general principles governing the adaptive response of individual cyanobacterial species to environmental perturbations across different scales, from a single organism to community, a systems-level analysis requires integration of critical information on key genetic and metabolic mechanisms [4]. Such an integrative approach resolves several challenges that currently face the functional genomic analysis of model microbes and cyanobacteria, in particular. It allows for more facile application of comparative genomics tools and knowledge transfer from well-studied eubacterial species, which is limited, at best, due significant difference in the genome structure and regulon organization of cyanobacteria [6]

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