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A Novel P-granule Protein Required for glh-1 and rde-4 mRNA Accumulation in the Germline Export

Development & Evolution Meeting (2006)

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caenorhabditis_elegans celegans c_elegans deps-1 elegans glh-1 meeting_abstract nematode pgl-1 t21g53 wormbase y65b4bl2 zk3814

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P granules are germ-cell-specific structures containing RNA and protein and required for proper germ cell development. We are interested in understanding how P granules are assembled or stabilized and whether they regulate mRNA translation or stability in germ cells. Mutations in glh-1, a gene encoding a VASA-like RNA helicase, fail to localize PGL-1 to P granules (Kawasaki et al. Cell 94, 635-645). Using EMS mutagenesis, we identified four mutations in a second gene (Y65B4BL.2) that reduce the accumulation of PGL-1 on P granules. We provisionally refer to this gene as dip-1 (diffuse PGL-1). Like pgl-1 and glh-1, dip-1 mutations cause germline underproliferation and temperature-sensitive maternal-effect sterility. Furthermore, glh-1 mRNA and protein levels are dramatically reduced in dip-1 mutants, suggesting that DIP-1 may be required to produce or stabilize glh-1 mRNAs. DIP-1 is a P-granule-associated protein, raising the exciting possibility that DIP-1 may link P granules to mRNA stability. We investigated this possibility by comparing the genome-wide expression profiles of isolated N2 and dip-1 germlines using microarrays. Although relatively few messages have altered abundances (either increased or decreased) in dip-1 mutant germlines, one gene that shows reduced mRNA accumlation is rde-4. Intriguingly, dip-1 mutants are resistant to pos-1(RNAi) and skn-1(RNAi) by feeding and we speculate that this is caused by a deficiency in RDE-4 protein accumulation in the germline.


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