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• W1997671657 endingPage "103" @default.
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• W1997671657 abstract "Organismal growth and body size are influenced by both genetic and environmental factors. We have utilized the strong molecular genetic techniques available in the nematode Caenorhabditis elegans to identify genetic determinants of body size. In C. elegans, DBL-1, a member of the conserved family of secreted growth factors known as the Transforming Growth Factor β superfamily, is known to play a major role in growth control. The mechanisms by which other determinants of body size function, however, is less well understood. To identify additional genes involved in body size regulation, a genetic screen for small mutants was previously performed. One of the genes identified in that screen was sma-21. We now demonstrate that sma-21 encodes ADT-2, a member of the ADAMTS (a disintegrin and metalloprotease with thrombospondin motifs) family of secreted metalloproteases. ADAMTS proteins are believed to remodel the extracellular matrix and may modulate the activity of extracellular signals. Genetic interactions suggest that ADT-2 acts in parallel with or in multiple size regulatory pathways. We demonstrate that ADT-2 is required for normal levels of expression of a DBL-1-responsive transcriptional reporter. We further demonstrate that adt-2 regulatory sequences drive expression in glial-like and vulval cells, and that ADT-2 activity is required for normal cuticle collagen fibril organization. We therefore propose that ADT-2 regulates body size both by modulating TGFβ signaling activity and by maintaining normal cuticle structure." @default.
• W1997671657 created "2016-06-24" @default.
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• W1997671657 date "2011-04-01" @default.
• W1997671657 modified "2023-10-17" @default.
• W1997671657 title "C. elegans ADAMTS ADT-2 regulates body size by modulating TGFβ signaling and cuticle collagen organization" @default.
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• W1997671657 doi "https://doi.org/10.1016/j.ydbio.2011.01.016" @default.
• W1997671657 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3049821" @default.
• W1997671657 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21256840" @default.
• W1997671657 hasPublicationYear "2011" @default.
• W1997671657 type Work @default.

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