RNA Binding Protein SRSF3 confers an essential role in megakaryocyte maturation and platelet production

Author:

Heazlewood Shen1,Ahmad Tanveer2ORCID,Mohenska Monika3,Guo Belinda B4ORCID,Gangatirkar Pradnya5,Josefsson Emma C6ORCID,Ellis Sarah7ORCID,Ratnadiwakara Madara8ORCID,Cao Huimin1,Cao Benjamin1,Heazlewood Chad1,Williams Brenda1,Fulton Madeline1,White Jacinta9ORCID,Ramialison Mirana3ORCID,Nilsson Susan K1,Anko Minna-Liisa8ORCID

Affiliation:

1. Australian Regenerative Medicine Institute, Monash University, VIC 3800, Australia, Australia

2. Biomedical Manufacturing CSIRO, VIC 3168, Australia, Australia

3. Monash University, Clayton, Australia

4. University of Western Australia, Crawley, Australia

5. Walter + Eliza Medical Research Institute, Melbourne, Australia

6. Department of Medical Biology, The University of Melbourne, VIC 3052, Australia, Australia

7. Olivia Newton-John Cancer Research Institute and School of Cancer Medicine, La Trobe University, VIC 3084, Australia, Australia

8. Department of Molecular and Translational Sciences, Monash University, VIC 3800, Australia, Australia

9. Commonwealth Scientific and Industrial Research Organisation, Melbourne, Australia

Abstract

RNA processing is increasingly recognised as a critical control point in the regulation of different haematopoietic lineages including megakaryocytes responsible for the production of platelets. Platelets are anucleate cytoplasts that contain a rich repertoire of RNAs encoding proteins with essential platelet functions derived from the parent megakaryocyte. It is largely unknown how RNA binding proteins contribute to the development and functions of megakaryocytes and platelets. We show that Serine-arginine rich splicing factor 3 (SRSF3) is essential for megakaryocyte maturation and generation of functional platelets. Megakaryocyte-specific deletion of Srsf3 in mice led to macrothrombocytopenia characterised by megakaryocyte maturation arrest, dramatically reduced platelet counts and abnormally large functionally compromised platelets. SRSF3 deficient megakaryocytes failed to reprogram their transcriptome during maturation and to load platelets with RNAs required for normal platelet function. SRSF3 depletion led to nuclear accumulation of megakaryocyte mRNAs demonstrating that SRSF3 deploys similar RNA regulatory mechanisms in megakaryocytes as in other cell types. Our study further suggests that SRSF3 plays a role in sorting cytoplasmic megakaryocyte RNAs into platelets and demonstrates how SRSF3-mediated RNA processing forms a central part of megakaryocyte gene regulation. Understanding SRSF3 functions in megakaryocytes and platelets provides key insights into normal thrombopoiesis and platelet pathologies as SRSF3 RNA targets in megakaryocytes are associated with platelet diseases.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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