Eukaryotic translation initiation factor eIF4E-5 is required for spermiogenesis inDrosophila melanogaster

Author:

Shao Lisa12ORCID,Fingerhut Jaclyn M.34ORCID,Falk Brook L.12ORCID,Han Hong5,Maldonado Giovanna6ORCID,Qiao Yuemeng17,Lee Vincent12ORCID,Hall Elizabeth12ORCID,Chen Liang5,Polevoy Gordon1ORCID,Hernández Greco6,Lasko Paul5ORCID,Brill Julie A.12ORCID

Affiliation:

1. The Hospital for Sick Children 1 Cell Biology Program , , PGCRL Building , 686 Bay Street, Toronto, Ontario, M5G 0A4 , Canada

2. University of Toronto 2 Department of Molecular Genetics , , 1 King's College Circle, Toronto, Ontario, M5S 1A8 , Canada

3. Whitehead Institute for Biomedical Research, Department of Biology, Massachusetts Institute of Technology 3 , 455 Main Street, Cambridge, MA 02142 , USA

4. Howard Hughes Medical Institute 4 , 455 Main Street, Cambridge, MA 02142 , USA

5. McGill University 5 Department of Biology , , 3649 Promenade Sir William Osler, Montréal, Quebec, H3G 0B1 , Canada

6. Instituto Nacional de Cancerología (INCan) 6 Laboratory of Translation and Cancer, Unit of Biomedical Research on Cancer , , Av San Fernando 22, Mexico City 14080 , Mexico

7. University of Toronto 7 Human Biology Program , , 300 Huron Street, Toronto, Ontario, M5S 3J6 , Canada

Abstract

ABSTRACTDrosophila sperm development is characterized by extensive post-transcriptional regulation whereby thousands of transcripts are preserved for translation during later stages. A key step in translation initiation is the binding of eukaryotic initiation factor 4E (eIF4E) to the 5′ mRNA cap. In addition to canonical eIF4E-1, Drosophila has multiple eIF4E paralogs, including four (eIF4E-3, -4, -5, and -7) that are highly expressed in the testis. Among these, only eIF4E-3 has been characterized genetically. Here, using CRISPR/Cas9 mutagenesis, we determined that eIF4E-5 is essential for male fertility. eIF4E-5 protein localizes to the distal ends of elongated spermatid cysts, and eIF4E-5 mutants exhibit defects during post-meiotic stages, including a mild defect in spermatid cyst polarization. eIF4E-5 mutants also have a fully penetrant defect in individualization, resulting in failure to produce mature sperm. Indeed, our data indicate that eIF4E-5 regulates non-apoptotic caspase activity during individualization by promoting local accumulation of the E3 ubiquitin ligase inhibitor Soti. Our results further extend the diversity of non-canonical eIF4Es that carry out distinct spatiotemporal roles during spermatogenesis.

Funder

SickKids Research Institute

Consejo Nacional de Ciencia y Tecnología

Instituto Nacional de Cancerología

Canadian Institutes of Health Research

Natural Sciences and Engineering Research Council of Canada

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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