Evolutionarily Conserved Polyadenosine RNA Binding Protein Nab2 Cooperates with Splicing Machinery To Regulate the Fate of Pre-mRNA

Author:

Soucek Sharon12,Zeng Yi34,Bellur Deepti L.4,Bergkessel Megan56,Morris Kevin J.12,Deng Qiudong27,Duong Duc27,Seyfried Nicholas T.27,Guthrie Christine6,Staley Jonathan P.4,Fasken Milo B.2,Corbett Anita H.2

Affiliation:

1. Graduate Program in Biochemistry, Cell, and Developmental Biology, Emory University School of Medicine, Atlanta, Georgia, USA

2. Department of Biochemistry, Emory University School of Medicine, Atlanta, Georgia, USA

3. Graduate Program in Cell and Molecular Biology, The University of Chicago, Chicago, Illinois, USA

4. Department of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, Illinois, USA

5. Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California, USA

6. Department of Biochemistry and Biophysics, University of California, San Francisco, California, USA

7. Center for Neurodegenerative Disease, Emory University School of Medicine, Atlanta, Georgia, USA

Abstract

ABSTRACT Numerous RNA binding proteins are deposited onto an mRNA transcript to modulate posttranscriptional processing events ensuring proper mRNA maturation. Defining the interplay between RNA binding proteins that couple mRNA biogenesis events is crucial for understanding how gene expression is regulated. To explore how RNA binding proteins control mRNA processing, we investigated a role for the evolutionarily conserved polyadenosine RNA binding protein, Nab2, in mRNA maturation within the nucleus. This study reveals that nab2 mutant cells accumulate intron-containing pre-mRNA in vivo . We extend this analysis to identify genetic interactions between mutant alleles of nab2 and genes encoding a splicing factor, MUD2 , and RNA exosome, RRP6 , with in vivo consequences of altered pre-mRNA splicing and poly(A) tail length control. As further evidence linking Nab2 proteins to splicing, an unbiased proteomic analysis of vertebrate Nab2, ZC3H14, identifies physical interactions with numerous components of the spliceosome. We validated the interaction between ZC3H14 and U2AF2/U2AF 65 . Taking all the findings into consideration, we present a model where Nab2/ZC3H14 interacts with spliceosome components to allow proper coupling of splicing with subsequent mRNA processing steps contributing to a kinetic proofreading step that allows properly processed mRNA to exit the nucleus and escape Rrp6-dependent degradation.

Funder

HHS | NIH | National Institute of General Medical Sciences

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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