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First published online 8 April 2004
doi: 10.1242/dev.01098
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1 Fox Chase Cancer Center, Philadelphia, PA 19111, USA
2 Department of Genetics, Dartmouth Medical School, Hanover, NH 03755, USA
3 Department of Molecular Biology, UMDNJ, Stratford, NJ 08084, USA
* Author for correspondence (e-mail: mosseg{at}umdnj.edu)
Accepted 28 January 2004
The succession of developmental events in the C. elegans larva is governed by the heterochronic genes. When mutated, these genes cause either precocious or retarded developmental phenotypes, in which stage-specific patterns of cell division and differentiation are either skipped or reiterated, respectively. We identified a new heterochronic gene, lin-46, from mutations that suppress the precocious phenotypes caused by mutations in the heterochronic genes lin-14 and lin-28. lin-46 mutants on their own display retarded phenotypes in which cell division patterns are reiterated and differentiation is prevented in certain cell lineages. Our analysis indicates that lin-46 acts at a step immediately downstream of lin-28, affecting both the regulation of the heterochronic gene pathway and execution of stage-specific developmental events at two stages: the third larval stage and adult. We also show that lin-46 is required prior to the third stage for normal adult cell fates, suggesting that it acts once to control fates at both stages, and that it affects adult fates through the let-7 branch of the heterochronic pathway. Interestingly, lin-46 encodes a protein homologous to MoeA of bacteria and the C-terminal domain of mammalian gephyrin, a multifunctional scaffolding protein. Our findings suggest that the LIN-46 protein acts as a scaffold for a multiprotein assembly that controls developmental timing, and expand the known roles of gephyrin-related proteins to development.
Key words: C. elegans, Larval development, Hypodermis, Heterochronic genes, lin-14, lin-28, lin-42, lin-46, lin-57, let-7, Gephyrin, MoeA, moc-1, moc-2
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