<i>ifet-1</i> is a broad scale translational repressor required for normal P granule formation in <i>C. elegans</i>

Madhu S. Sengupta, Wai Yee Low, Joseph R. Patterson, Hyun‐Min Kim, Ana Traven, Traude H. Beilharz, Mónica P. Colaiácovo, Jennifer A Schisa, Peter R. Boag

Journal of Cell Science · 2012 · 39 citations · 47 references

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Abstract

Large cytoplasmic ribonucleoprotein germ granule complexes are a common feature in germ cells. In C. elegans these are called P granules and for much of the life-cycle they associate with nuclear pore complexes in germ cells. P granules are rich in proteins that function in diverse RNA pathways. Here we report that the C. elegans homolog of the eIF4E-transporter IFET-1 is required for oogenesis but not spermatogenesis. We show that IFET-1 is required for translational repression of several maternal mRNAs in the distal gonad and functions in conjunction with the broad-scale translational regulators CGH-1, CAR-1 and PATR-1 to regulate germ cell sex determination. Furthermore we have found that IFET-1 localizes to P granules throughout the gonad and in the germ cell lineage in the embryo. Interestingly, IFET-1 is required for the normal ultrastructure of P granules and for the localization of CGH-1 and CAR-1 to P granules. Our findings suggest that IFET-1 is a key translational regulator and is required for normal P granule formation.

References

47