Cell competition corrects noisy Wnt morphogen gradients to achieve robust patterning in the zebrafish embryo.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 31624259.
- Also identified by DOI 10.1038/s41467-019-12609-4 and PMC identifier 6797755.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Morphogen signalling forms an activity gradient and instructs cell identities in a signalling strength-dependent manner to pattern developing tissues. However, developing tissues also undergo dynamic morphogenesis, which may produce cells with unfit morphogen signalling and consequent noisy morphogen gradients. Here we show that a cell competition-related system corrects such noisy morphogen gradients. Zebrafish imaging analyses of the Wnt/β-catenin signalling gradient, which acts as a morphogen to establish embryonic anterior-posterior patterning, identify that unfit cells with abnormal Wnt/β-catenin activity spontaneously appear and produce noise in the gradient. Communication between unfit and neighbouring fit cells via cadherin proteins stimulates apoptosis of the unfit cells by activating Smad signalling and reactive oxygen species production. This unfit cell elimination is required for proper Wnt/β-catenin gradient formation and consequent anterior-posterior patterning. Because this gradient controls patterning not only in the embryo but also in adult tissues, this system may support tissue robustness and disease prevention.
Medical subject headings
- Body Patterning
- Embryo, Nonmammalian
- Gene Expression Regulation, Developmental
- Morphogenesis
- Wnt Signaling Pathway
- Zebrafish Proteins
- beta Catenin