共 14 条
Selective nuclear export of mRNAs is promoted by DRBD18 in Trypanosoma brucei
被引:9
|作者:
Mishra, Amartya
[1
]
Kaur, Jan Naseer
[1
]
McSkimming, Daniel I.
[2
]
Hegedusova, Eva
[3
]
Dubey, Ashutosh P.
[1
]
Ciganda, Martin
[1
]
Paris, Zdenek
[3
,4
]
Read, Laurie K.
[1
]
机构:
[1] Univ Buffalo, Jacobs Sch Med & Biomed Sci, Buffalo, NY 14260 USA
[2] Univ S Florida, Bioinformat & Computat Biol Core, Tampa, FL USA
[3] Czech Acad Sci, Ctr Biol, Inst Parasitol, Ceske Budejovice, Czech Republic
[4] Univ South Bohemia, Fac Sci, Ceske Budejovice, Czech Republic
关键词:
FISH;
mRNA export;
nucleoporin;
RNA binding protein;
RNAseq;
trypanosome;
SR PROTEINS;
BINDING;
TRANSPORT;
COMPLEX;
MEX67-MTR2;
DECAY;
D O I:
10.1111/mmi.14773
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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.
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页码:827 / 840
页数:14
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