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gld-1, a tumor suppressor gene required for oocyte development in Caenorhabditis elegans. Export

Genetics, Vol. 139 (1995), pp. 579-606.

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article caenorhabditis_elegans celegans c_elegans elegans genes_dominant_genetics genes_helminth_genetics genes_helminth_physiology genes_suppressor_tumor_genetics genes_suppressor_tumor_physiology genetic_complementation_test germ_cells_physiology germinoma gld-1 hermaphroditism meiosis mitosis mutation_physiology nematode oogenesis_genetics phenotype sex_differentiation_genetics spermatogenesis_genetics t23g113 wormbase

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We have characterized 31 mutations in the gld-1 (defective in germline development) gene of Caenorhabditis elegans. In gld-1 (null) hermaphrodites, oogenesis is abolished and a germline tumor forms where oocyte development would normally occur. By contrast, gld-1 (null) males are unaffected. The hermaphrodite germline tumor appears to derive from germ cells that enter the meiotic pathway normally but then exit pachytene and return to the mitotic cycle. Certain gld-1 partial loss-of-function mutations also abolish oogenesis, but germ cells arrest in pachytene rather than returning to mitosis. Our results indicate that gld-1 is a tumor suppressor gene required for oocyte development. The tumorous phenotype suggests that gld-1(+) may function to negatively regulate proliferation during meiotic prophase and/or act to direct progression through meiotic prophase. We also show that gld-1(+) has an additional nonessential role in germline sex determination: promotion of hermaphrodite spermatogenesis. This function of gld-1 is inferred from a haplo-insufficient phenotype and from the properties of gain-of-function gld-1 mutations that cause alterations in the sexual identity of germ


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