act operon control of developmental gene expression in Myxococcus xanthus
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Updated: Oct 2, 2026

Fluorescence Live-cell Imaging of the Complete Vegetative Cell Cycle of the Slow-growing Social Bacterium Myxococcus xanthus
Published on: June 20, 2018
Thomas M A Gronewold1, Dale Kaiser
1Departments of Biochemistry and of Developmental Biology, Stanford University School of Medicine, Stanford, California 94305-5329, USA.
Abstract:
Cell-bound C-signal guides the building of a fruiting body and triggers the differentiation of myxospores. Earlier work has shown that transcription of the csgA gene, which encodes the C-signal, is directed by four genes of the act operon. To see how expression of the genes encoding components of the aggregation and sporulation processes depends on C-signaling, mutants with loss-of-function mutations in each of the act genes were investigated. These mutations were found to have no effect on genes that are normally expressed up to 3 h into development and are C-signal independent. Neither the time of first expression nor the rate of expression increase was changed in actA, actB, actC, or actD mutant strains. Also, there was no effect on A-signal production, which normally starts before 3 h. By contrast, the null act mutants have striking defects in C-signal production. These mutations changed the expression of four gene reporters that are related to aggregation and sporulation and are expressed at 6 h or later in development. The actA and actB null mutations substantially decreased the expression of all these reporters. The other act null mutations caused either premature expression to wild-type levels (actC) or delayed expression (actD), which ultimately rose to wild-type levels. The pattern of effects on these reporters shows how the C-signal differentially regulates the steps that together build a fruiting body and differentiate spores within it.
Insights
The four genes of the act operon are crucial for C-signal production, which guides fruiting body development and spore differentiation in myxobacteria. Mutations in these genes disrupt C-signal dependent gene expression, impacting aggregation and sporulation processes.
Area of Science:
- Cellular and Molecular Biology
- Developmental Biology
- Microbiology
Background:
- Cell-bound C-signal is essential for fruiting body formation and myxospore differentiation.
- The csgA gene, encoding the C-signal, is regulated by four genes within the act operon.
- Understanding the dependence of aggregation and sporulation genes on C-signaling is key to deciphering developmental pathways.
Purpose of the Study:
- To investigate how the expression of aggregation and sporulation genes is affected by mutations in the act operon genes.
- To determine the role of the act operon in C-signal production and its downstream effects.
- To elucidate the regulatory mechanisms of C-signal in coordinating developmental processes.
Main Methods:
- Generation and analysis of loss-of-function mutants in each of the four act operon genes.
- Monitoring the expression of C-signal independent and dependent genes using reporter assays.
- Assessing the impact of mutations on A-signal production and C-signal synthesis.
Main Results:
- Act operon mutations did not affect early developmental genes (expressed before 3h) or A-signal production.
- Null act mutants exhibited significant defects in C-signal production.
- Mutations in actA and actB reduced expression of late developmental reporters, while actC and actD mutations altered the timing of reporter expression.
Conclusions:
- The act operon genes are essential for C-signal production, which differentially regulates aggregation and sporulation.
- C-signaling plays a critical role in the temporal control of developmental gene expression.
- The findings provide insights into the intricate regulatory network governing myxobacterial development.
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