| Literature DB >> 35942683 |
Takayoshi Yamamoto1, Yuta Kambayashi1, Yuta Otsuka2, Boni A Afouda3, Claudiu Giuraniuc3, Tatsuo Michiue1,2, Stefan Hoppler3.
Abstract
Secreted molecules called morphogens govern tissue patterning in a concentration-dependent manner. However, it is still unclear how reproducible patterning can be achieved with diffusing molecules, especially when that patterning concerns differentiation of thin tissues. Wnt is a morphogen that organizes cardiac development. Wnt6 patterns cardiogenic mesoderm to induce differentiation of a thin tissue, the pericardium, in Xenopus. In this study, we revealed that a Wnt receptor, frizzled-7, is expressed in a Wnt-dependent manner. With a combination of experiments and mathematical modeling, this receptor-feedback appears essential to shape a steep gradient of Wnt signaling. In addition, computer simulation revealed that this feedback imparts robustness against variations of Wnt ligand production and allows the system to reach a steady state quickly. We also found that a Wnt antagonist sFRP1, which is expressed on the opposite side of the Wnt source, accumulates on N-acetyl-rich heparan sulfate (HS). N-acetyl-rich HS concentration is high between the sources of Wnt and sFRP1, achieving local inhibition of Wnt signaling via restriction of sFRP1 spreading. These integrated regulatory systems restrict the Wnt signaling range and ensure reproducible patterning of the thin pericardium.Entities:
Keywords: Wnt signal; Xenopus; developmental biology; frizzled; gene regulatory circuit; heart; morphogen; xenopus
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Year: 2022 PMID: 35942683 PMCID: PMC9363125 DOI: 10.7554/eLife.73818
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.713