Search bioRxiv⌕ Search

Biology subjects

Oster, L. D.

Publications and source records attributed to Oster, L. D..

2 recordsLinked to original sources

Endosome motility controls light-responsive reproductive development and secondary metabolite production in Aspergillus

Filamentous fungi, such as Aspergillus species, use microtubule transport to move early endosomes. Other cargos, such as peroxisomes and mRNAs, "hitchhike" on early endosomes to move throughout the long hyphae of these organisms. In Aspergillus nidulans, peroxisomes hitchhike on early endosomes using the endosomal protein PxdA and the peroxisomal protein AcbdA. The HookA adaptor protein links endosomes to microtubule motors. Here, we set out to explore the physiological functions of peroxisome hitchhiking and endosome motility. Aspergillus nidulans has a complex life cycle that includes asexual and sexual reproduction. A. nidulans and other fungi within the Pezizomycotina subphylum are also notable for the vast number of secondary metabolites they produce. Light and other environmental conditions influence developmental decisions and secondary metabolite production. Here, we found that sexual reproduction is favored in the absence of endosome motility, even in the light, which normally promotes asexual reproduction. RNA sequencing of strains lacking PxdA-marked motile early endosomes showed altered expression of genes involved in development. Unexpectedly, we also observed altered expression of genes involved in secondary metabolism in strains lacking endosome motility and peroxisome hitchhiking. Using mass spectrometry, we found that the loss of endosome motility affected the biosynthesis of secondary metabolites, including sterigmatocystin, a carcinogenic mycotoxin that is a food contaminant. Finally, in a pathogenic species, Aspergillus fumigatus, we found that deletion of its pxdA homolog also significantly altered secondary metabolite production. Our work uncovers an unexpected link between organelle motility, developmental decisions in response to light, and secondary metabolite production in filamentous fungi.

cell biology↗

Filopodia numbers impact chemotactic migration speed

Migrating cells sense and respond to external chemical and physical cues, enabling them to efficiently reach their destinations. Filopodia are slender actin-filled membrane protrusions implicated in interacting with the extracellular environment in many contexts, such as neuronal growth cone guidance and the capture of prey by immune cells and unicellular organisms. The role of filopodia in chemotactic guidance in fast-moving amoeboid cells has not been well-studied. The social amoeba Dictyostelium relies on chemotaxis for development and finding food, making it an excellent system for investigating the role of filopodia in amoeboid chemotaxis. Stimulation of amoebae with the chemoattractant cAMP activates a transient increase of filopodia formation by recruiting the filopodial myosin DdMyo7 to the cell cortex. Filopodia formation is biased towards the source of chemoattractant, yet myo7 null cells that lack filopodia exhibit normal directional migration. However, cells either lacking filopodia or having increased numbers of filopodia move more slowly than those with wildtype numbers of filopodia. Thus, while filopodia are dispensable for detection of chemical gradients by amoeboid cells, changes in filopodia number can impact their migration speed possibly due to altering cell-substrate adhesion. In briefFilopodia formation in chemotactic amoeboid cells is stimulated by chemoattractant and biased towards the gradient source. Lack of filopodia does not impair directed migration but rather reduces cell speed. Changes in filopodia number correlate with the speed of chemotactic cells suggesting a role for these extension in tuning adhesion for optimal migration. HighlightsO_LIFilopodia formation in chemotactic amoeboid cells is biased towards the source of the gradient. C_LIO_LIChemotactic Dictyostelium amoebae lacking filopodia migrate with directional persistence. C_LIO_LIMigration speed is altered by filopodia number. C_LI

cell biology↗