Eukaryotic Cell
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EC Accepts, published online ahead of print on 5 October 2007
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EC.00176-07v1
6/12/2206    most recent
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Eukaryotic Cell doi:10.1128/EC.00176-07
Copyright (c) 2007, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

T. brucei RNA binding proteins, p34 and p37, mediate NOPP44/46 cellular localization via the exportin 1 nuclear export pathway

Kristina Hellman, Kimberly Prohaska, and Noreen Williams*

Department of Microbiology and Immunology & Witebsky Center for Microbial Pathogenesis and Immunology, 253 Biomedical Research Building, University at Buffalo, Buffalo, NY 14214, USA

* To whom correspondence should be addressed. Email: nw1{at}acsu.buffalo.edu.


   Abstract

We have previously identified and characterized two novel nuclear RNA binding proteins, p34 and p37, which have been shown to interact with a family of nucleolar phosphoproteins, NOPP44/46, in Trypanosoma brucei. These proteins are nearly identical, the major difference being an 18 amino acid insert in the N-terminus of p37. In order to characterize the interaction between p34 and p37 and NOPP44/46, we have utilized an RNA interference cell line that specifically targets p34 and p37. Within these RNAi cells, we detected a disruption of a higher molecular weight complex containing NOPP44/46, as well as a dramatic increase in nuclear NOPP44/46 protein levels. We demonstrated that no change occurred in NOPP44/46 mRNA steady state levels or stability, nor was there a change in cellular protein levels. These results led us to investigate whether p34 and p37 regulate NOPP44/46 cellular localization. Examination of the p34 and p37 amino acid sequences revealed a leucine-rich nuclear export signal, which interacts with the nuclear export factor, exportin 1. Immune capture experiments demonstrated that p34, p37, and NOPP44/46 associate with exportin 1. When performed with p34/p37 RNAi cells, NOPP44/46 no longer associated with exportin 1. Sequential immune capture experiments demonstrated that p34, p37, NOPP44/46, and exportin 1 exist in a common complex. Inhibiting exportin 1-mediated nuclear export led to an increase in nuclear NOPP44/46 proteins, indicating that they are exported from the nucleus via this pathway. Together, our results demonstrate that p34 and p37 regulate NOPP44/46 cellular localization by facilitating their association with exportin 1.







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