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Araujo, S. J.

Publications and source records attributed to Araujo, S. J..

3 recordsLinked to original sources

Centriole Loss in Embryonic Development Disrupts Axonal Pathfinding and Muscle Integrity

Centrosomes, the primary microtubule-organizing centres (MTOCs), are important during early neuronal development, contributing to polarity establishment and axon formation. Although once considered dispensable in differentiated cells, accumulating evidence suggests that centrosomes remain active in many cell types, with functions that depend on cellular context. In mammalian neurons, centrosome-dependent microtubule (MT) remodelling has been implicated in axon elongation, and centrosome dysfunction has been associated with axonal guidance defects. While active centrosomes have been observed in Drosophila melanogaster tracheal cells, their neuronal activity in vivo has remained unclear. Here, we examined Drosophila Sas-4 mutants, which undergo gradual centrosome loss (CL), and found that 50% of homozygous mutants fail to hatch. Analysis revealed the presence of centrosomes in wild-type motor and sensory neurons, with centrosomes localizing near nascent axons in motor neurons. Embryonic CL altered axonal routing and muscle organization, and targeted Sas-4 reduction in pioneer neurons produced mild guidance phenotypes. Centrosome MTOC activity was confirmed by tubulin localization and MT reassembly analyses. In addition, CL was associated with increased motor axon tortuosity, consistent with a contribution of centrosomes to neuronal morphology. Together, these findings indicate that centrosomes, while not acting as essential MTOCs in this context, contribute to MT dynamics and aspects of early axonal and muscle development.

cell biology↗

Coordinated crosstalk between microtubules and actin by a spectraplakin regulates lumen formation and branching

The establishment of branched structures by single cells involves complex cytoskeletal remodelling events. In Drosophila, epithelial tracheal system terminal cells (TCs) and dendritic arborisation neurons are models for these subcellular branching processes. During tracheal embryonic development, the generation of subcellular branches is characterized by extensive remodelling of the microtubule (MT) network and actin cytoskeleton, followed by vesicular transport and membrane dynamics. We have previously shown that centrosomes are key players in the initiation of subcellular lumen formation where they act as microtubule organizing centres (MTOCs). However, not much is known on the events that lead to the growth of these subcellular luminal branches or what makes them progress through a particular trajectory within the cytoplasm of the TC. Here, we have identified that the spectraplakin Short-stop (Shot) promotes the crosstalk between MTs and actin, which leads to the extension and guidance of the subcellular lumen within the TC cytoplasm. Shot is enriched in cells undergoing the initial steps of subcellular branching as a direct response to FGF signalling. An excess of Shot induces ectopic acentrosomal branching points in the embryonic and larval tracheal TC leading to cells with extra subcellular lumina. These data provide the first evidence for a role for spectraplakins in subcellular lumen formation and branching.

cell biology↗

Blimp-1 mediates the temporal control of embryonic tube maturation

The specification of tissue identity during embryonic development requires precise spatiotemporal coordination of gene expression. Many transcription factors required for the development of organs have been identified and their expression patterns are known; however, the mechanisms through which they coordinate gene expression in time remain poorly understood. Here we show that hormone-induced transcription factor Blimp-1 participates in the temporal coordination of tubulogenesis in Drosophila melanogaster by regulating the expression of many genes involved in tube maturation. In particular, we demonstrate that Blimp-1 regulates the expression of genes involved in chitin deposition and F-actin organization. We show that Blimp-1 is involved in the temporal control of lumen maturation by regulating the beginning of chitin deposition. We also report that Blimp-1 represses a variety of genes involved in tracheal maturation. Finally, we reveal that the kinase Btk29A serves as a link between Blimp-1 transcriptional repression and apical extra-cellular matrix organization.

developmental biology↗