SDE2 is an essential gene required for ribosome biogenesis and the regulation of alternative splicing

Author:

Floro Jess1,Dai Anqi12,Metzger Abigail1,Mora-Martin Alexandra3,Ganem Neil J1,Cifuentes Daniel3,Wu Ching-Shyi4,Dalal Jasbir3,Lyons Shawn M3ORCID,Labadorf Adam25,Flynn Rachel L1ORCID

Affiliation:

1. Departments of Pharmacology and Experimental Therapeutics, and Medicine, Cancer Center, Boston University School of Medicine, Boston, MA 02118, USA

2. Bioinformatics Program, Boston University, Boston, MA 02118 USA

3. Department of Biochemistry, Boston University School of Medicine, Boston, MA 02118, USA

4. Department and Graduate Institute of Pharmacology, National Taiwan University College of Medicine, Taipei, 10051, Taiwan

5. Department of Neurology, Boston University School of Medicine, Boston, MA 02118 USA

Abstract

Abstract RNA provides the framework for the assembly of some of the most intricate macromolecular complexes within the cell, including the spliceosome and the mature ribosome. The assembly of these complexes relies on the coordinated association of RNA with hundreds of trans-acting protein factors. While some of these trans-acting factors are RNA-binding proteins (RBPs), others are adaptor proteins, and others still, function as both. Defects in the assembly of these complexes results in a number of human pathologies including neurodegeneration and cancer. Here, we demonstrate that Silencing Defective 2 (SDE2) is both an RNA binding protein and also a trans-acting adaptor protein that functions to regulate RNA splicing and ribosome biogenesis. SDE2 depletion leads to widespread changes in alternative splicing, defects in ribosome biogenesis and ultimately complete loss of cell viability. Our data highlight SDE2 as a previously uncharacterized essential gene required for the assembly and maturation of the complexes that carry out two of the most fundamental processes in mammalian cells.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics

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