TABLE 2.
The 13 different pathways/processes examined in this study as determinants of the social behavior in model Myxococcota genomes, along with the number of genes in each module, and the percentage of genes identified in Zodletone genomes as well as the genomes of three Myxococcota type species known to exhibit nonsocial behaviora,b
Major function in the social lifestyle | Process/pathway | No. of genes in module | Zodletone lineages (%) |
Type species (nonsocial) (%) |
Notes on homologues identified/missing in Zodletone genomes |
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---|---|---|---|---|---|---|---|---|---|
O__JAFGXQ01 | F__JAFGIB01 | Anaeromyxobacter dehalogenes | Labilithrix luteola | Vulgatibacter incomptus | Homologues identified | Homologues missing | |||
Gene regulatory networks governing early events of aggregation and mound formation prior to sporulation | Enhancer-binding protein (EBP) module | 9 | 88.9 | 88.9 | 88.9 | 100 | 88.9 | 8 total: 6 DNA-binding transcriptional response regulator domains of the NtrC family, 1 serine/threonine kinases, and 1 peptidase | ActC (one of the Act group of proteins) |
MrpC module | 8 | 75 | 62.5 | 75 | 75 | 87.5 | 2 catalytic domains of serine/threonine kinases, 2 component system sensor histidine kinases, an oligopeptide transporter, and a DNA-binding transcriptional response regulator of the NtrC family | MrpC, a transcription factor that works cooperatively to control the start of sporulation | |
Nla24 module | 2 | 100 | 100 | 100 | 100 | 100 | A DNA-binding transcriptional response regulator of the NtrC family and a diguanylate-cyclase (DGC) or GGDEF domain | ||
FruA module | 1 | 0 | 0 | 0 | 0 | 0 | FruA, a transcription factor that works cooperatively to control the start of sporulation | ||
Exopolysaccharide production necessary for the formation of fruiting bodies | EPS production | 8 | 12.5 | 12.5 | 50 | 100 | 62.5 | 1 homologue identified with a sugar transporter domain | 7 out of 8 homologues missing |
Extracellular signal production | C-signal | 3 | 0 | 0 | 0 | 0 | 0 | All proteins in this module: CsgA encoding the actual C-signal protein, the activating protease PopC, and its inhibitor PopD | |
A-signal | 8 | 25 | 25 | 75 | 75 | 75 | 2 DNA-binding transcriptional response regulators of the NtrC family | A-signal production-specific homologues | |
Gene regulatory networks governing sporulation | Aggregation, sporulation, fruiting body formation | 35 | 11.4 | 11.4 | 40 | 22.9 | 42.7 | 1 sugar transporter and 3 transcriptional regulators | The majority of sporulation-specific genes The dev operon CRISPR-Cas genes The Exo and Nfs genes (both involved in forming the spore polysaccharide coat) The spore coat protein Tps The putative FAD-binding monooxygenase MXA2872 FruA-MrpC-regulated genes (Fmg) mcu operon encoding a chaperone/usher secretion system important for spore-coat assembly |
Coordination of the two motility systems (Frz) and induction of Nla24 module (Dif) | Chemosensory pathways | 17 | 35.3 | 35.3 | 40 | 25.7 | 31.4 | 1 Dif gene and 3 Frz genes identified, mainly due to their similarity to chemotaxis protein histidine kinases, chemotaxis methyltransferase, and methylesterase Two of the three cell-polarity regulatory proteins were identified, a small GTPase, and its cognate GTPase activator |
5 of the 6 Dif chemosensory network homologues The cytoplasmic receptor for the Frz chemosensory network FrzCD, the 2 coupling proteins FrzA and FrzB, the dual response regulator protein FrzZ that localizes to the cell poles and interact with the 3 cell-polarity regulatory proteins 1 of the 3 cell-polarity regulatory proteins (RomR) |
Fine tuning and optimizing the onset of aggregation and sporulation | Development timers | 6 | 50 | 50 | 83.3 | 83.3 | 83.3 | RodK and 2 of the RedCDEF, a 4-component system necessary for controlling aggregation timing Homologues are similar to sensor histidine kinase (n = 2), and a helix-turn-helix-containing response regulator |
2 of the RedCDEF, a 4-component system necessary for controlling aggregation timing. |
Motility | Adventurous (A) motility | 18 | 33.3 | 27.8 | 77.8 | 38.9 | 88.9 | 3 Glt complex genes and 2 Agl complex genes (similarity to TolQR/ExbBD/MotAB-like channel) | AglZ that contributes to the assembly of the inner membrane complex CglB, the lipoprotein interacting with the substratum at focal adhesion sites GltA, B, H, K (outer membrane beta barrel structures that transport the lipoprotein CglB to the external surface) AglQS (inner membrane complex) |
Social (S) motility | 14 | 57.1 | 57.1 | 71.4 | 64.3 | 64.3 | S motility is mediated by type IV pili (T4P) The majority of T4P genes were identified |
PilA (the major pilin), PilI, and PilO | |
Sharing of resources, kin-recognition for exclusion of cheaters | Outer membrane exchange (OME) | 2 | 50 | 50 | 50 | 100 | 50 | TraA partner, TraB, was identified mainly because it contains an outer membrane OmpA domain | TraA, the cell surface receptor, was not identified in Zodletone genomes. |
More details are in the supplementary text and Table S6.
The cells with percentage of genes identified are color coded as follows: dark gray with white font, >50% of the pathway was identified in the genome; light gray, 25 to 50% of the pathway was identified in the genome; white, <25% of the pathway was identified in the genome.