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

Bühlmann, M; Walrad, Pegine; Rico, E; Ivens, A; Capewell, P; Naguleswaran, Arunasalam; Roditi, Isabel; Matthews, K (2015). NMD3 regulates both mRNA and rRNA nuclear export in African trypanosomes via an XPOI-linked pathway. Nucleic acids research, 43(9), pp. 4491-4504. Oxford University Press 10.1093/nar/gkv330

[img]
Preview
Text
Roditi_Naguleswaran.pdf - Published Version
Available under License Creative Commons: Attribution (CC-BY).

Download (6MB) | Preview
[img]
Preview
Text
gkv330.pdf - Other
Available under License Creative Commons: Attribution (CC-BY).

Download (6MB) | Preview

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.

Item Type:

Journal Article (Original Article)

Division/Institute:

08 Faculty of Science > Department of Biology > Institute of Cell Biology

UniBE Contributor:

Naguleswaran, Arunasalam, Roditi, Isabel

Subjects:

500 Science > 570 Life sciences; biology

ISSN:

0305-1048

Publisher:

Oxford University Press

Funders:

[4] Swiss National Science Foundation ; [UNSPECIFIED] Swiss National Science Foundation ; [UNSPECIFIED] Howard Hughes Medical Institute

Language:

English

Submitter:

Isabel Roditi

Date Deposited:

08 May 2015 12:00

Last Modified:

05 Dec 2022 14:47

Publisher DOI:

10.1093/nar/gkv330

PubMed ID:

25873624

BORIS DOI:

10.7892/boris.68789

URI:

https://boris.unibe.ch/id/eprint/68789

Actions (login required)

Edit item Edit item
Provide Feedback