NMD3 regulates both mRNA and rRNA nuclear export in African trypanosomes via an XPOI-linked pathway.

Nucleic Acids Res

Centre for Immunity, Infection and Evolution, Institute for Immunology and Infection Research, School of Biological Sciences, Kings Buildings, University of Edinburgh, West Mains Road, Edinburgh EH9 3JT, UK

Published: May 2015

AI Article Synopsis

  • - Trypanosomes mainly control gene expression through post-transcriptional methods, especially by regulating mRNA stability and its export from the nucleus, which is crucial for gene regulation.
  • - The study found that depleting TbNMD3, which is involved in rRNA processing and export, leads to increased levels of procyclin-associated gene mRNAs due to altered nuclear export, rather than changes in transcription or translation.
  • - Analysis indicates that this mechanism of regulation operates through the 5'UTR of PAG1 mRNA and involves nuclear export factors, suggesting that mRNA and rRNA might share a common export pathway linked to NMD3.

Article Abstract

Trypanosomes mostly regulate gene expression through post-transcriptional mechanisms, particularly mRNA stability. However, much mRNA degradation is cytoplasmic such that mRNA nuclear export must represent an important level of regulation. Ribosomal RNAs must also be exported from the nucleus and the trypanosome orthologue of NMD3 has been confirmed to be involved in rRNA processing and export, matching its function in other organisms. Surprisingly, we found that TbNMD3 depletion also generates mRNA accumulation of procyclin-associated genes (PAGs), these being co-transcribed by RNA polymerase I with the procyclin surface antigen genes expressed on trypanosome insect forms. By whole transcriptome RNA-seq analysis of TbNMD3-depleted cells we confirm the regulation of the PAG transcripts by TbNMD3 and using reporter constructs reveal that PAG1 regulation is mediated by its 5'UTR. Dissection of the mechanism of regulation demonstrates that it is not dependent upon translational inhibition mediated by TbNMD3 depletion nor enhanced transcription. However, depletion of the nuclear export factors XPO1 or MEX67 recapitulates the effects of TbNMD3 depletion on PAG mRNAs and mRNAs accumulated in the nucleus of TbNMD3-depleted cells. These results invoke a novel RNA regulatory mechanism involving the NMD3-dependent nuclear export of mRNA cargos, suggesting a shared platform for mRNA and rRNA export.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482084PMC
http://dx.doi.org/10.1093/nar/gkv330DOI Listing

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