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Herdman, M.

Publications and source records attributed to Herdman, M..

2 recordsLinked to original sources

Complex interplay between gene deletions and the environment uncovers cellular roles for genes of unknown function in Escherichia coli

Phenotypic outcomes can be heavily affected by environmental factors. In this study, we exploited the previously observed nutrient-dependency of cell biological phenotypic features, captured by a cross-condition image-based profiling assay of Escherichia coli deletion strains, to examine this in more detail. We identified several general principles, including the existence of a spectrum of deviating phenotypes across nutrient conditions (i.e., from nutrient- or feature-specific to pleiotropic phenotypic deviations), limited conservation of phenotypic deviations across nutrient conditions (i.e., limited phenotypic robustness), and a subset of nutrient-independent phenotypic deviations (indicative of consistent genetic determinants of specific phenotypic features). In a subsequent step, we used this cross-condition dataset to identify five genes of unknown function of which the deletion displayed either nutrient-independent phenotypic deviations or phenotypic similarities to genes of known function: yibN, yaaY, yfaQ, ybiJ, and yijD. These genes showed different levels of phylogenetic conservation, ranging from conserved across the tree of life (yibN) to only present in some genera of the Enterobacterales (yaaY). Analysis of the structural properties of the proteins encoded by these y-genes, identification of structural similarities to other proteins, and the examination of their subcellular localization yielded new insights into their contribution to E. coli cell morphogenesis, cell cycle progression and cell growth. Together, our approach showcases how bacterial image-based profiling assays and datasets can serve as a gateway to reveal the function of uncharacterized proteins. ImportanceDespite unprecedented access to genomic information, predicting phenotypes based on genotypes remains notoriously difficult. One major confounding factor is the environment and its ability to modulate phenotypic outcomes. Another is the fact that a large fraction of protein-coding genes in bacterial genomes remains uncharacterized and have no known function. In this work, we use a large-scale cross-condition image-based profiling dataset to characterize nutrient-dependent phenotypic variability of E. coli deletion strains and exploit it to provide insight into the cellular role of genes of unknown function. Through our analysis, we identified five genes of unknown function that we subsequently further characterized by examining their phylogenetic conservation, predicted structural properties and similarities, and their intracellular localization. Combined, this approach highlights the potential of cross-condition image-based profiling, which extracts many cell biological phenotypic readouts across multiple conditions, to better understand nutrient-dependent phenotypic variability and uncover protein function.

microbiology↗

Cell Cycle Dependent Orchestration of Surface Layer Biogenesis in Caulobacter crescentus

Surface layers (S-layers) are proteinaceous, two-dimensional crystals that constitute the outermost components of many prokaryotic cell envelopes. In this study, we investigated principles of S-layer biogenesis on the outer membrane in the bacterial model organism Caulobacter crescentus. Fluorescent microscopy revealed localised incorporation of new S-layer at the poles and mid-cell, consistent with elongation and division phases of the cell cycle. Next, light microscopy and electron cryotomography investigations of drug-treated bacteria revealed that bacterial actin homologue MreB is crucial for localised S-layer insertion. We further uncovered that S-layer biogenesis follows new peptidoglycan synthesis and localises to regions of high cell wall turnover. Finally, correlated cryo-light microscopy and electron cryotomographic analysis of regions of S-layer insertion showed the presence of gaps in the hexagonal S-layer lattice, contrasting with other S-layers completed by defined symmetric defects. Our findings provide insight into how C. crescentus cells form an ordered S-layer on their surface, providing evidence for coordination between the biogenesis of the cell envelope at multiple levels.

microbiology↗