RT Journal Article
SR Electronic
T1 Ectoderm to mesoderm transition by downregulation of actomyosin contractility
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 870444
DO 10.1101/870444
A1 Leily Kashkooli
A1 David Rozema
A1 Lina Espejo-Ramirez
A1 Paul Lasko
A1 François Fagotto
YR 2019
UL http://biorxiv.org/content/early/2019/12/11/870444.abstract
AB Collective migration of cohesive tissues is a fundamental process in morphogenesis, and is particularly well illustrated during gastrulation by the rapid and massive internalization of the mesoderm, which contrasts with the much more modest movements of the ectoderm. In the Xenopus embryo, the differences in morphogenetic capabilities of ectoderm and mesoderm can be connected to the properties of individual cells, which, when studied in vitro, show opposite intrinsic organizations, cohesive for ectoderm, dispersive for mesoderm. Surprisingly, we find these seemingly deep differences can be accounted for simply by differences in Rock-dependent actomyosin contractility. We show that Rock inhibition is sufficient to rapidly unleash motility in the ectoderm and confer it with mesoderm-like properties. In the mesoderm, this motility is dependent on two RhoA negative regulators, the small GTPase Rnd1 and the RhoGAP Shirin/Dlc2/ArhGAP37. Both are absolutely essential for gastrulation. At the cellular and tissue level, the two regulators show overlapping yet distinct functions. They both contribute to decrease cortical tension and confer motility, but Shirin tends to increase tissue fluidity and stimulate dispersion, while Rnd1 tends to favour more compact collective migration. Thus, each is able to contribute to a specific property of the migratory behaviour of the mesoderm.