Abstract
AbstractMechanosensitive ion channels play an essential role in reacting to environmental signals and sustaining cell integrity by facilitating ion flux across membranes. For obligate intracellular pathogens like microsporidia, adapting to changes in host environment is crucial for survival and propagation. Despite representing a eukaryote of extreme genome reduction, microsporidia have expanded the gene family of mechanosensitive ion channels of small conductance (mscS) through repeated gene duplication and horizontal gene transfer. All microsporidian genomes that are characterized to-date containmscSgenes of both eukaryotic and bacterial origin, and have at least 5 differentmscScopies. Here, we investigated the cryo-electron microscopy structure of the bacterially derived mechanosensitive ion channel of small conductance 2 (MscS2) fromNematocida displodere, an intracellular pathogen ofCaenorhabditis elegans. MscS2 is the most compact MscS known, and assembles into a unique superstructurein vitrowith six heptameric MscS2 channels oligomerizing through their transmembrane domains. Individual MscS2 channels are oriented in a heterogeneous manner to one another, resembling an asymmetric, flexible six-way cross joint. Finally, we show that, despite the extreme compaction, microsporidian MscS2 still forms a heptameric membrane channel, conserving the most important structural features of bacterial MscS.
Publisher
Cold Spring Harbor Laboratory