Search bioRxiv⌕ Search

Biology subjects

Rauzi, M.

Publications and source records attributed to Rauzi, M..

2 recordsLinked to original sources

A mechanical wave travels along a genetic guide to drive the formation of an epithelial furrow

Epithelial furrowing is a morphogenetic process that is pivotal during embryo gastrulation, neurulation and the shaping of the animal body. A furrow often results from a fold that propagates along a line. How fold formation and propagation are initiated, driven and controlled is still poorly understood. To shed new light on this fundamental morphogenetic process, we study the formation of the cephalic furrow: a fold that runs along the dorsal-ventral axis of the embryo during early Drosophila gastrulation and the developmental role of which is still unknown. Here, we provide evidence of its function and show that the cephalic furrow is initiated by two groups of cells located on the left and right lateral sides of the embryo. These cellular clusters work as a pacemaker triggering a bi-directional morphogenetic wave powered by actomyosin contractions and sustained by de novo medial apex-to-apex cell adhesion. The Cartesian position of the pacemakers is under the cross-control of the embryo anterior-posterior and dorsal-ventral gene patterning systems. Thus, furrow initiation and propagation are driven by a mechanical trigger wave that travels under the control of a multidimensional genetic guide.

developmental biology↗

Embryo-scale epithelial buckling forms a propagating furrow that initiates gastrulation

Cell apical constriction driven by actomyosin contraction forces is a conserved mechanism during tissue folding in embryo development. While much effort has been made to better understand the molecular mechanisms responsible for apical constriction, it is still not clear if apical actomyosin contraction forces are necessary or sufficient per se to drive tissue folding. To tackle this question, we use the Drosophila embryo model system that forms a furrow on the ventral side, initiating mesoderm internalization. Past computational models support the idea that cell apical contraction forces may not be sufficient and that active or passive cell apico-basal forces may be necessary to drive cell wedging and tissue furrowing. By using 3D computational modelling and in toto embryo image analysis and manipulation, we now challenge this idea and show that embryo-scale force balance of the tissue surface, rather than cell-autonomous shape changes, is necessary and sufficient to drive a buckling of the epithelial surface forming a furrow which propagates and initiates embryo gastrulation.

developmental biology↗