Summary of ssbd-repos-00030

SSBD:database
URL

Name
ssbd-repos-00030 (30-Inomata-CellDyn)
URL
DOI
-

Title
-
Description
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Submited Date
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Release Date
2017-10-03
Updated Date
2018-11-15
License
Funding information
-
File formats
Data size
1.2 GB

Organism
X. laevis
Strain
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Cell Line
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Genes
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Proteins
Chordin, Noggin, Sizzled, TM

GO Molecular Function (MF)
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GO Biological Process (BP)
NA (protein diffusion)
GO Cellular Component (CC)
NA
Study Type
-
Imaging Methods
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Method Summary
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Related paper(s)

Hidehiko Inomata, Tatsuo Shibata, Tomoko Haraguchi, Yoshiki Sasai (2013) Scaling of dorsal-ventral patterning by embryo size-dependent degradation of Spemann's organizer signals., Cell, Volume 153, Number 6, pp. 1296-311

Published in 2013 Jun 6

(Abstract) Spemann's organizer plays a key role in dorsal-ventral (DV) patterning in the amphibian embryo by secreting diffusible proteins such as Chordin, an antagonist to ventralizing bone morphogenetic proteins (BMPs). The DV patterning is so robust that an amphibian embryo with its ventral half surgically removed can develop into a smaller but proportionally patterned larva. Here, we show that this robust patterning depends on facilitated Chordin degradation and requires the expression of the Chordin-proteinase inhibitor Sizzled on the opposite side. Sizzled, which is stable and diffuses widely along the DV axis, stabilizes Chordin and expands its distribution in the ventral direction. This expanded Chordin distribution, in turn, limits BMP-dependent Sizzled production, forming an axis-wide feedback loop for shaping Chordin's activity. Using bisection assays, we demonstrate that Chordin degradation is dynamically controlled by embryo-size-coupled Sizzled accumulation. We propose a scaling model that enables the DV pattern to adjust proportionally to embryonic axis size.
(MeSH Terms)

Contact(s)
Hidehiko Inomata
Organization(s)
RIKEN , Center for Developmental Biology , Laboratory for Physical Biology
Image Data Contributors
Quantitative Data Contributors

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