Germ-line induction of the Caenorhabditis elegans vulva
- *Cellular and Molecular Biology Program, †Department of Biochemistry, and ‡Howard Hughes Medical Institute, University of Wisconsin, 433 Babcock Drive, Madison, WI 53706
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Contributed by Judith Kimble, November 30, 2005
Abstract
Development of the Caenorhabditis elegans vulva serves as a paradigm for intercellular signaling during animal development. In wild-type animals, the somatic gonadal anchor cell generates the LIN-3/EGF ligand to induce vulval fates in the underlying hypodermis, whereas FBF, FOG-1, and FOG-3 control germ-line development. Here we report that FBF functions redundantly with FOG-1 and FOG-3 to control vulval induction: animals lacking FBF and either FOG-1 or FOG-3 have multiple vulvae, the Muv phenotype. The fog; fbf Muv phenotype is generated by aberrant induction of vulval precursor cells (VPCs): in wild-type animals, three VPCs are induced to form a single vulva, but, in fog; fbf mutants, four or five VPCs are typically induced, resulting in ectopic vulvae. Laser ablation experiments and mosaic analyses demonstrate that the germ line is critical for the fog; fbf Muv phenotype. Consistent with that site of action, we detect FBF and FOG-1 in the germ line but not in the VPCs. The simplest interpretation is that FOG-1, FOG-3, and FBF act in the germ line to influence vulval fates. The LIN-3/EGF ligand may be the germ-line signal to the VPCs: the fog; fbf Muv phenotype depends on LIN-3 activity, and the lin-3 3′ UTR possesses an FBF binding element. Our findings reveal new insights into germ line-to-soma signals and the role of PUF proteins in animal development.
Footnotes
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↵ § To whom correspondence should be addressed. E-mail: jekimble{at}wisc.edu.
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Conflict of interest statement: No conflicts declared.
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Abbreviations: FBF, fem-3 binding factor; VPC, vulval precursor cell; AC, anchor cell; FBE, FBF binding element; RNAi, RNA interference.
- Copyright © 2006, The National Academy of Sciences





