Sulfatase modifying factors control the timing of zebrafish convergence and extension morphogenesis

Convergence and extension (C&E) cell movements that elongate the primary embryonic axis are precisely timed during vertebrate gastrulation, but mechanisms controlling their onset remain unknown. Using zebrafish embryonic explants that recapitulate C&E and its timing, we identified sulfatase modifying factor 2 (sumf2) as a candidate trigger gene for C&E onset. sumf2 and its paralog sumf1 encode negative and positive sulfatase regulators, respectively, whose expression levels invert and increase heparan sulfate sulfation during gastrulation. Overexpressing sumf1 or sumf2 causes delayed or precocious C&E, respectively, whereas their loss shifts C&E timing in the opposite direction. We identified Sulf1, a modifier of heparan sulfate proteoglycans (HSPGs), as their key downstream effector and found that altering heparan sulfate sulfation levels shifts C&E onset and suppresses sumf1 and sumf2 mutant phenotypes. This work supports a model in which sumf2 expression reduces sulfatase activity, rewriting HSPG sulfation patterns to promote the onset of C&E morphogenesis.

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Publication Details

Journal
Nature Communications
Published
2026-03-31
DOI
https://doi.org/10.1038/s41467-026-70804-6
Primary Topic
Proteoglycans and glycosaminoglycans research
Type
article
Field-Weighted Citation Impact
0.00

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article

Sulfatase modifying factors control the timing of zebrafish convergence and extension morphogenesis

Ryan J. Weiss, Margot Williams, Cristian Coarfa, Sandra L. Grimm et al.
Nature Communications
Proteoglycans and glycosaminoglycans research
article

Sulfatase modifying factors control the timing of zebrafish convergence and extension morphogenesis

Ryan J. Weiss, Margot Williams, Cristian Coarfa, Sandra L. Grimm, Ailen S. Cervino, Gursimran Kaur Bajwa, Rubén Marín-Juez, Amrita Basu
article en

Abstract

Convergence and extension (C&E) cell movements that elongate the primary embryonic axis are precisely timed during vertebrate gastrulation, but mechanisms controlling their onset remain unknown. Using zebrafish embryonic explants that recapitulate C&E and its timing, we identified sulfatase modifying factor 2 (sumf2) as a candidate trigger gene for C&E onset. sumf2 and its paralog sumf1 encode negative and positive sulfatase regulators, respectively, whose expression levels invert and increase heparan sulfate sulfation during gastrulation. Overexpressing sumf1 or sumf2 causes delayed or precocious C&E, respectively, whereas their loss shifts C&E timing in the opposite direction. We identified Sulf1, a modifier of heparan sulfate proteoglycans (HSPGs), as their key downstream effector and found that altering heparan sulfate sulfation levels shifts C&E onset and suppresses sumf1 and sumf2 mutant phenotypes. This work supports a model in which sumf2 expression reduces sulfatase activity, rewriting HSPG sulfation patterns to promote the onset of C&E morphogenesis.

Nature Communications
University of Georgia (US), Baylor College of Medicine (US), Centre Hospitalier Universitaire Sainte-Justine (CA), Université de Montréal (CA)
Cancer Prevention and Research Institute of Texas, Fonds de Recherche du Québec-Société et Culture, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Environmental Health Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Openalex Percentile: Top 28%
Proteoglycans and glycosaminoglycans research
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