Literature DB >> 21613532

The Tpr protein regulates export of mRNAs with retained introns that traffic through the Nxf1 pathway.

John H Coyle1, Yeou-Cherng Bor, David Rekosh, Marie-Louise Hammarskjold.   

Abstract

Post-transcriptional regulation of mRNA includes restriction mechanisms to prevent export and expression of mRNAs that are incompletely spliced. Here we present evidence that the mammalian protein Tpr is involved in this restriction. To study the role of Tpr in export of mRNA with retained introns, we used reporters in which the mRNA was exported either via the Nxf1/Nxt1 pathway using a CTE or via the Crm1 pathway using Rev/RRE. Our data show that even modest knockdown of Tpr using RNAi leads to a significant increase in export and translation from the mRNA containing the CTE. In contrast, Tpr perturbation has no effect on export of mRNA containing the RRE, either in the absence or presence of Rev. Also, no effects were observed on export of a completely spliced mRNA. Taken together, our results indicate that Tpr plays an important role in quality control of mRNA trafficked on the Nxf1 pathway.

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Year:  2011        PMID: 21613532      PMCID: PMC3138570          DOI: 10.1261/rna.2616111

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  63 in total

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  47 in total

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