| Literature DB >> 32079657 |
Hayden P Huggins1, Jacob S Subash1, Hamilton Stoffel1, Melissa A Henderson2, Jenna L Hoffman1, David S Buckner1, Madhu S Sengupta3, Peter R Boag3, Myon-Hee Lee4, Brett D Keiper5.
Abstract
Germ cells use both positive and negative mRNA translational control to regulate gene expression that drives their differentiation into gametes. mRNA translational control is mediated by RNA-binding proteins, miRNAs and translation initiation factors. We have uncovered the discrete roles of two translation initiation factor eIF4E isoforms (IFE-1, IFE-3) that bind 7-methylguanosine (m7G) mRNA caps during Caenorhabditis elegans germline development. IFE-3 plays important roles in germline sex determination (GSD), where it promotes oocyte cell fate and is dispensable for spermatogenesis. IFE-3 is expressed throughout the germline and localizes to germ granules, but is distinct from IFE-1 and PGL-1, and facilitates oocyte growth and viability. This contrasts with the robust expression in spermatocytes of IFE-1, the isoform that resides within P granules in spermatocytes and oocytes, and promotes late spermatogenesis. Each eIF4E is localized by its cognate eIF4E-binding protein (IFE-1:PGL-1 and IFE-3:IFET-1). IFE-3 and IFET-1 regulate translation of several GSD mRNAs, but not those under control of IFE-1. Distinct mutant phenotypes, in vivo localization and differential mRNA translation suggest independent dormant and active periods for each eIF4E isoform in the germline.Entities:
Keywords: 4EBP; Gametogenesis; Germline sex determination; Polysomes; eIF4E; mRNA translational control
Mesh:
Substances:
Year: 2020 PMID: 32079657 PMCID: PMC7132772 DOI: 10.1242/jcs.237990
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285