The eukaryotic translation initiation factor eIF4E reprograms alternative splicing

Mehdi Ghram, Gavin Morris, Biljana Culjkovic-Kraljacic, Jean Clement Mars, Patrick Gendron, Lucy Skrabanek, Maria Victoria Revuelta, Leandro Cerchietti, Monica L. Guzman, Katherine L.B. Borden*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Aberrant splicing is typically attributed to splice-factor (SF) mutation and contributes to malignancies including acute myeloid leukemia (AML). Here, we discovered a mutation-independent means to extensively reprogram alternative splicing (AS). We showed that the dysregulated expression of eukaryotic translation initiation factor eIF4E elevated selective splice-factor production, thereby impacting multiple spliceosome complexes, including factors mutated in AML such as SF3B1 and U2AF1. These changes generated a splicing landscape that predominantly supported altered splice-site selection for ~800 transcripts in cell lines and ~4,600 transcripts in specimens from high-eIF4E AML patients otherwise harboring no known SF mutations. Nuclear RNA immunoprecipitations, export assays, polysome analyses, and mutational studies together revealed that eIF4E primarily increased SF production via its nuclear RNA export activity. By contrast, eIF4E dysregulation did not induce known SF mutations or alter spliceosome number. eIF4E interacted with the spliceosome and some pre-mRNAs, suggesting its direct involvement in specific splicing events. eIF4E induced simultaneous effects on numerous SF proteins, resulting in a much larger range of splicing alterations than in the case of mutation or dysregulation of individual SFs and providing a novel paradigm for splicing control and dysregulation.

Original languageEnglish (US)
Article numbere110496
JournalEMBO Journal
Volume42
Issue number7
DOIs
StatePublished - Apr 3 2023

Funding

We are grateful for assistance from the Genomics Platform at IRIC. Primary human specimens were obtained from the Banque de cellules leucémiques du Québec (BCLQ), supported by the Cancer Research Network of the Fonds de Recherche du Québec—Santé (FRQS). KLBB acknowledges funding from Leukemia and Lymphoma Society United States and Canada (TRP R6513-20), the Canadian Institutes for Health Research (PJT 159785), and was supported by the National Cancer Institutes of Health under Award numbers RO1CA098571 and RO1CA080728, the content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. KLBB holds a Canada Research Chair in Molecular Biology of the Cell Nucleus (950-231848), and MG holds Cole Foundation and Baumgartner fellowships and JC a Bourse postdoctorale Power Corporation du Canada de la relève scientifique. We are grateful for assistance from the Genomics Platform at IRIC. Primary human specimens were obtained from the Banque de cellules leucémiques du Québec (BCLQ), supported by the Cancer Research Network of the Fonds de Recherche du Québec—Santé (FRQS). KLBB acknowledges funding from Leukemia and Lymphoma Society United States and Canada (TRP R6513‐20), the Canadian Institutes for Health Research (PJT 159785), and was supported by the National Cancer Institutes of Health under Award numbers RO1CA098571 and RO1CA080728, the content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. KLBB holds a Canada Research Chair in Molecular Biology of the Cell Nucleus (950‐231848), and MG holds Cole Foundation and Baumgartner fellowships and JC a Bourse postdoctorale Power Corporation du Canada de la relève scientifique. MG, GM, BCK, JCM, PG, LS, MVR, LC, MLG, and KLBB have no disclosure or competing interests. Of note, BCK and KLBB hold patents related to ribavirin use in AML; however, they have received no royalties or other benefit from these: Combination therapy using ribavirin as elF4E inhibitor, Inventors: Katherine Borden, Hiba Zahreddine, Biljana Culjkovic‐Kraljacic (targeting inducible drug glucuronidation). US10342817B2; translation dysfunction‐based therapeutic inventors: Gordon Jamieson, Katherine Borden, Biljana Culjkovic, Alex Kentsis: US8497292B2. KLBB has held Leukemia and Lymphoma Society and NIH funds listed above to study AML. MGL has research funding and consulting from BridgeMedicines, Equity SeqRX, LLC, and holds other AML funding from the NIH (R21CA245454 and R01CA234478).

Keywords

  • acute myeloid leukemia
  • eIF4E
  • splicing

ASJC Scopus subject areas

  • General Neuroscience
  • Molecular Biology
  • General Biochemistry, Genetics and Molecular Biology
  • General Immunology and Microbiology

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