Please use this identifier to cite or link to this item: https://doi.org/10.1242/dev.019794
Title: The pro-domain of the zebrafish Nodal-related protein cyclops regulates its signaling activities
Authors: Tian, J.
Andrée, B.
Jones, C.M.
Sampath, K. 
Keywords: Cyclops
Left-right asymmetry
Mature domain
Nodal signaling
Pro-domain
Squint
Zebrafish
Issue Date: Aug-2008
Citation: Tian, J., Andrée, B., Jones, C.M., Sampath, K. (2008-08). The pro-domain of the zebrafish Nodal-related protein cyclops regulates its signaling activities. Development 135 (15) : 2649-2658. ScholarBank@NUS Repository. https://doi.org/10.1242/dev.019794
Abstract: Nodal proteins are secreted signaling factors of the transforming growth factor β (TGFβ) family with essential roles in embryonic development in vertebrates. Mutations affecting the Nodal factors have severe consequences in mammals and fish. Furthermore, increased Nodal levels have been associated with melanoma tumor progression. Like other TGFβ-related proteins, Nodal factors consist of a pro-domain and a mature domain. The pro-domain of mouse Nodal protein stabilizes its precursor. However, the mechanisms by which the pro-domains exert their activities are unknown. Here, we characterize the zebrafish Nodal-related factor Cyclops (Cyc) and find unexpected functions for the pro-domain in regulating Cyc activity. We identified a lysosome-targeting region in the Cyc pro-domain that destabilizes the precursor and restricts Cyc activity, revealing the molecular basis for the short- range signaling activities of Cyc. We show that both the pro- and mature-domains of Cyc regulate its stability. We also characterize a mutation in the pro-domain of human NODAL (hNODAL) that underlies congenital heterotaxia. Heterologous expression of mutant hNODAL increases expression of Nodal-response genes. Our studies reveal unexpected roles for the pro-domain of the Nodal factors and provide a possible mechanism for familial heterotaxia.
Source Title: Development
URI: http://scholarbank.nus.edu.sg/handle/10635/101990
ISSN: 09501991
DOI: 10.1242/dev.019794
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