ifet-1 is a broad scale translational repressor required for normal P granule formation in C. elegans
Author(s) -
Madhu S. Sengupta,
Wai Yee Low,
Joseph R. Patterson,
HyunMin Kim,
Ana Traven,
Traude H. Beilharz,
Mónica P. Colaiácovo,
Jennifer A Schisa,
Peter R. Boag
Publication year - 2012
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.119834
Subject(s) - biology , microbiology and biotechnology , granule (geology) , ribonucleoprotein , germ cell , stress granule , somatic cell , translational regulation , rna binding protein , regulator , oogenesis , oocyte , messenger rna , embryo , rna , genetics , translation (biology) , gene , paleontology
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.
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