Abstract

BackgroundThe genetic network involved in the bacterial cell cycle is poorly understood even though it underpins the remarkable ability of bacteria to proliferate. How such network evolves is even less clear. The major aims of this work were to identify and examine the genes and pathways that are differentially expressed during the Caulobacter crescentus cell cycle, and to analyze the evolutionary features of the cell cycle network.ResultsWe used deep RNA sequencing to obtain high coverage RNA-Seq data of five C. crescentus cell cycle stages, each with three biological replicates. We found that 1,586 genes (over a third of the genome) display significant differential expression between stages. This gene list, which contains many genes previously unknown for their cell cycle regulation, includes almost half of the genes involved in primary metabolism, suggesting that these “house-keeping” genes are not constitutively transcribed during the cell cycle, as often assumed. Gene and module co-expression clustering reveal co-regulated pathways and suggest functionally coupled genes. In addition, an evolutionary analysis of the cell cycle network shows a high correlation between co-expression and co-evolution. Most co-expression modules have strong phylogenetic signals, with broadly conserved genes and clade-specific genes predominating different substructures of the cell cycle co-expression network. We also found that conserved genes tend to determine the expression profile of their module.ConclusionWe describe the first phylogenetic and single-nucleotide-resolution transcriptomic analysis of a bacterial cell cycle network. In addition, the study suggests how evolution has shaped this network and provides direct biological network support that selective pressure is not on individual genes but rather on the relationship between genes, which highlights the importance of integrating phylogenetic analysis into biological network studies.

Highlights

  • The genetic network involved in the bacterial cell cycle is poorly understood even though it underpins the remarkable ability of bacteria to proliferate

  • Single-nucleotide resolution whole-genome mapping of RNA sequencing (RNA-Seq) To examine the cell cycle transcriptome of C. crescentus, cells grown in the M2G minimal medium were subjected to Ludox density centrifugation to isolate swarmer (G1 phase) cells, which were re-suspended in M2G medium to resume cell cycle progression synchronously

  • Samples were collected for RNA extraction at 5 different time points (0, 30, 60, 90, and 120 min) following synchronization, with each time point corresponding to a different cell cycle stage referred to as swarmer (SW), stalked (ST), early predivisional (EPD), predivisional (PD), and late predivisional (LPD) (Figure 1)

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Summary

Introduction

The genetic network involved in the bacterial cell cycle is poorly understood even though it underpins the remarkable ability of bacteria to proliferate. How such network evolves is even less clear. Advances in next-generation sequencing methodologies have significantly reduced the time and cost constraints of determining genome-wide expression levels of various organisms, including bacteria. These technologies present major advantages over hybridization-based microarrays [1,2]. The SW cell reiterates the aforementioned cell cycle whereas the ST cell skips the G1 phase and initiates the S phase immediately

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