The Orphan Histidine Kinase TodK Influences Myxococcus xanthus Multicellular Development by Inactivating the CRP /Fnr Homolog, MrpC

Environmental bacteria have abundant signaling systems wired into complex gene regulatory networks to adapt to fluctuating conditions. In Myxococcus xanthus, starvation triggers a developmental program (specialized biofilm) that produces spore-filled multicellular fruiting bodies surrounded by a distinct quiescent state termed peripheral rods. Fruiting body structure as well as the proportion of cells following each fate can be tuned by a large repertoire of signaling proteins, including numerous orphan histidine kinases. Here, we focus on the histidine kinase TodK, which was previously demonstrated to influence developmental progression. We find that loss of TodK produces distinct developmental phenotypes that vary with environmental conditions. To quantify these effects, we developed an image-analysis pipeline that measures aggregation and fruiting body patterning during development on nutrient-limited agar. These analyses revealed the todK mutant prematurely aggregates particularly at the peripheries of the colony. Under submerged-culture conditions, initial production of aggregates was observed with wild-type timing, but these aggregates displayed accelerated transition to mature fruiting bodies. Overexpression of active TodK completely blocked fruiting body formation. Molecular analyses demonstrated that TodK overproduction suppressed expression of core developmental regulators including FruA and CsgA. Interestingly, protein accumulation of MrpC, a transcription factor necessary for expression of both FruA and CsgA, was not significantly perturbed. These data suggest TodK silences MrpC's ability to activate transcription of key developmental targets. Together, these findings establish TodK as a modulator of developmental progression and demonstrate how quantitative phenotyping approaches can reveal biologically meaningful functions for orphan histidine kinases whose mutant phenotypes might otherwise appear subtle.

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Publication Details

Journal
Molecular Microbiology
Published
2026-09-14
DOI
https://doi.org/10.1111/mmi.70115
Primary Topic
Bacterial Genetics and Biotechnology
Type
article
Field-Weighted Citation Impact
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article

The Orphan Histidine Kinase TodK Influences Myxococcus xanthus Multicellular Development by Inactivating the CRP /Fnr Homolog, MrpC

Penelope I. Higgs, Stuart Huntley, Christopher Mataczynski, Maike Glaser
Molecular Microbiology
Bacterial Genetics and Biotechnology
article

The Orphan Histidine Kinase TodK Influences Myxococcus xanthus Multicellular Development by Inactivating the CRP /Fnr Homolog, MrpC

Penelope I. Higgs, Stuart Huntley, Christopher Mataczynski, Maike Glaser
article en

Abstract

Environmental bacteria have abundant signaling systems wired into complex gene regulatory networks to adapt to fluctuating conditions. In Myxococcus xanthus, starvation triggers a developmental program (specialized biofilm) that produces spore-filled multicellular fruiting bodies surrounded by a distinct quiescent state termed peripheral rods. Fruiting body structure as well as the proportion of cells following each fate can be tuned by a large repertoire of signaling proteins, including numerous orphan histidine kinases. Here, we focus on the histidine kinase TodK, which was previously demonstrated to influence developmental progression. We find that loss of TodK produces distinct developmental phenotypes that vary with environmental conditions. To quantify these effects, we developed an image-analysis pipeline that measures aggregation and fruiting body patterning during development on nutrient-limited agar. These analyses revealed the todK mutant prematurely aggregates particularly at the peripheries of the colony. Under submerged-culture conditions, initial production of aggregates was observed with wild-type timing, but these aggregates displayed accelerated transition to mature fruiting bodies. Overexpression of active TodK completely blocked fruiting body formation. Molecular analyses demonstrated that TodK overproduction suppressed expression of core developmental regulators including FruA and CsgA. Interestingly, protein accumulation of MrpC, a transcription factor necessary for expression of both FruA and CsgA, was not significantly perturbed. These data suggest TodK silences MrpC's ability to activate transcription of key developmental targets. Together, these findings establish TodK as a modulator of developmental progression and demonstrate how quantitative phenotyping approaches can reveal biologically meaningful functions for orphan histidine kinases whose mutant phenotypes might otherwise appear subtle.

Molecular Microbiology
Wayne State University (US), Cranbrook Academy of Art (US), Michigan Reproductive Medicine (US)
Life in Land
Openalex Percentile: Top 11%
Bacterial Genetics and Biotechnology
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