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Selective nuclear export of mRNAs is promoted by DRBD18 in Trypanosoma brucei
A. Mishra, JN. Kaur, DI. McSkimming, E. Hegedűsová, AP. Dubey, M. Ciganda, Z. Paris, LK. Read
Language English Country Great Britain
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
R01 AI141557
NIAID NIH HHS - United States
NLK
Free Medical Journals
from 1997 to 18 months ago
Wiley Free Content
from 1997 to 18 months ago
PubMed
34146438
DOI
10.1111/mmi.14773
Knihovny.cz E-resources
- MeSH
- Active Transport, Cell Nucleus MeSH
- Gene Knockdown Techniques methods MeSH
- Membrane Transport Proteins metabolism MeSH
- RNA, Messenger metabolism MeSH
- Nucleocytoplasmic Transport Proteins metabolism MeSH
- RNA-Binding Proteins genetics metabolism MeSH
- Protozoan Proteins genetics metabolism MeSH
- Gene Expression Regulation MeSH
- RNA, Transfer metabolism MeSH
- Transcriptome MeSH
- RNA Transport MeSH
- Trypanosoma brucei brucei genetics metabolism MeSH
- Protein Binding MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
Kinetoplastids, including Trypanosoma brucei, control gene expression primarily at the posttranscriptional level. Nuclear mRNA export is an important, but understudied, step in this process. The general heterodimeric export factors, Mex67/Mtr2, function in the export of mRNAs and tRNAs in T. brucei, but RNA binding proteins (RBPs) that regulate export processes by controlling the dynamics of Mex67/Mtr2 ribonucleoprotein formation or transport have not been identified. Here, we report that DRBD18, an essential and abundant T. brucei RBP, associates with Mex67/Mtr2 in vivo, likely through its direct interaction with Mtr2. DRBD18 downregulation results in partial accumulation of poly(A)+ mRNA in the nucleus, but has no effect on the localization of intron-containing or mature tRNAs. Comprehensive analysis of transcriptomes from whole-cell and cytosol in DRBD18 knockdown parasites demonstrates that depletion of DRBD18 leads to impairment of nuclear export of a subset of mRNAs. CLIP experiments reveal the association of DRBD18 with several of these mRNAs. Moreover, DRBD18 knockdown leads to a partial accumulation of the Mex67/Mtr2 export receptors in the nucleus. Taken together, the current study supports a model in which DRBD18 regulates the selective nuclear export of mRNAs by promoting the mobilization of export competent mRNPs to the cytosol through the nuclear pore complex.
Bioinformatics and Computational Biology Core University of Southern Florida Tampa FL USA
Faculty of Science University of South Bohemia České Budějovice Czech Republic
Institute of Parasitology Biology Centre Czech Academy of Sciences České Budějovice Czech Republic
Jacobs School of Medicine and Biomedical Sciences University at Buffalo Buffalo NY USA
References provided by Crossref.org
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