A model for boundary-driven tissue morphogenesis

成果类型:
Article
署名作者:
Alber, Daniel S.; Zhao, Shiheng; Jacinto, Alexandre O.; Wieschaus, Eric F.; Shvartsman, Stanislav Y.; Haas, Pierre A.
署名单位:
Princeton University; Princeton University; Max Planck Society; Max Planck Society; Simons Foundation; Flatiron Institute; Princeton University
刊物名称:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
ISSN/ISSBN:
0027-10966
DOI:
10.1073/pnas.2505160122
发表日期:
2025-09-23
关键词:
cell-shape changes ventral furrow sea-urchin drosophila gastrulation forces intercalation invagination expression EVOLUTION
摘要:
Tissue deformations during morphogenesis can be active, driven by internal processes, or passive, resulting from stresses applied at their boundaries. Here, we introduce the Drosophila hindgut primordium as a model for studying boundary-driven tissue morphogenesis. We characterize its deformations and show that its complex shape changes can be a passive consequence of the deformations of the active regions of the embryo that surround it. First, we find an intermediate characteristic triangular keyhole shape in the 3D deformations of the hindgut. We construct a minimal model of the hindgut primordium as an elastic ring deformed by active midgut invagination and germ band extension on an ellipsoidal surface, which robustly captures the symmetry-breaking into this triangular keyhole shape. We then quantify the 3D kinematics of the tissue by a set of contours and find that the hindgut deforms in two stages: An initial translation on the curved embryo surface followed by a rapid breaking of shape symmetry. We extend our model to show that the contour kinematics in both stages are consistent with our passive picture. Our results suggest that the role of in-plane deformations during hindgut morphogenesis is to translate the tissue to a region with anisotropic embryonic curvature and show that uniform boundary conditions are sufficient to generate the observed nonuniform shape change. Our work thus provides a possible explanation for the various characteristic shapes of blastoporeequivalents in different organisms and a framework for the mechanical emergence of global morphologies in complex developmental systems.