Protein kinase VRK-1 regulates cell invasion and EGL-17/FGF signaling in Caenorhabditis elegans

Autor: Paul W. Sternberg, Peter Askjaer, Pilar Alarcón, Valerie Reinke, Katherine Waters, Elke P. F. Klerkx
Jazyk: angličtina
Rok vydání: 2009
Předmět:
Zdroj: Digital.CSIC. Repositorio Institucional del CSIC
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Popis: 11 pages, 6 figures.-- PMID: 19679119 [PubMed].-- Printed version published Nov 1, 2009.
Supporting information available at: http://dx.doi.org/10.1016/j.ydbio.2009.08.007
The vaccinia-related kinases (VRKs) are highly conserved throughout the animal kingdom and phosphorylate several chromatin proteins and transcription factors. In early Caenorhabditis elegans embryos, VRK-1 is required for proper nuclear envelope formation. In this work, we present the first investigation of the developmental role of VRKs by means of a novel C. elegans vrk-1 mutant allele. We found that VRK-1 is essential in hermaphrodites for formation of the vulva, uterus, and utse and for development and maintenance of the somatic gonad and thus the germ line. VRK-1 regulates anchor cell polarity and the timing of anchor cell invasion through the basement membranes separating vulval and somatic gonadal cells during the L3 larval stage. VRK-1 is also required for proper specification and proliferation of uterine cells and sex myoblasts. Expression of the fibroblast growth factor-like protein EGL-17 and its receptor EGL-15 is reduced in vrk-1 mutants, suggesting that VRK-1 might act at least partially through activation of FGF signaling. Expression of a translational VRK-1::GFP fusion protein in the ventral nerve cord and vulva precursor cells restores vulva and uterus formation, suggesting both cell autonomous and non-autonomous roles of VRK-1.
This work was funded by grants from the Spanish Ministry of Science (RYC-2003-001521, BFU-2004-01096, BFU-2007-60116) to PA. In addition, we wish to acknowledge EMBO and the Boehringer Ingelheim Foundation for support to EK and Junta de Andalucía for institutional support. PWS is an investigator with the Howard Hughes Medical Institute. Some nematode strains used in this work were provided by the International C. elegans Gene Knockout Consortium and the Caenorhabditis Genetics Center, which is funded by the NIH National Center for Research Resources (NCRR).
Databáze: OpenAIRE