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.
引用
收藏
页码:827 / 840
页数:14
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