Tdrd3 is a novel stress granule-associated protein interacting with the Fragile-X syndrome protein FMRP

被引:65
作者
Linder, Bastian [1 ]
Ploettner, Oliver [2 ]
Kroiss, Matthias [1 ]
Hartmann, Enno [3 ]
Laggerbauer, Bernhard [1 ]
Meister, Gunter [2 ]
Keidel, Eva [2 ]
Fischer, Utz [1 ]
机构
[1] Theodor Boveri Inst, Dept Biochem, D-97074 Wurzburg, Germany
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[3] Med Univ Lubeck, Inst Biol, D-23538 Lubeck, Germany
关键词
D O I
10.1093/hmg/ddn219
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
Tudor domains are widespread among proteins involved in RNA metabolism, but only in a few cases their cellular function has been analyzed in detail. Here, we report on the characterization of the ubiquitously expressed Tudor domain containing protein Tdrd3. Apart from its Tudor domain, we show that Tdrd3 possesses an oligosaccharide/nucleotide binding fold (OB-fold) and an ubiquitin associated domain capable of binding tetra-ubiquitin. A set of biochemical experiments revealed an interaction of Tdrd3 with FMRP, the product of the gene affected in Fragile X syndrome, and its autosomal homologs FXR1 and FXR2. FMRP has been implicated in the translational regulation of target mRNAs and shown to be a component of stress granules (SG). We demonstrate that overexpression of Tdrd3 in cells induces the formation of SGs and as a result leads to its co-localization with endogenous FMRP in these structures. Interestingly, the disease-associated FMRP missense mutation I304N identified in a Fragile X patient severely impairs the interaction with Tdrd3 in biochemical experiments. We propose a contribution of Tdrd3 to FMRP-mediated translational repression and suggest that the loss of the FMRP-Tdrd3 interaction caused by the I304N mutation might contribute to the pathogenesis of Fragile X syndrome.
引用
收藏
页码:3236 / 3246
页数:11
相关论文
共 39 条
[21]   The deacetylase HDAC6 is a novel critical component of stress granules involved in the stress response [J].
Kwon, SoHee ;
Zhang, Yu ;
Matthias, Patrick .
GENES & DEVELOPMENT, 2007, 21 (24) :3381-3394
[22]   Evidence that fragile X mental retardation protein is a negative regulator of translation [J].
Laggerbauer, B ;
Ostareck, D ;
Keidel, EM ;
Ostareck-Lederer, A ;
Fischer, U .
HUMAN MOLECULAR GENETICS, 2001, 10 (04) :329-338
[23]   Complex RNA processing of TDRKH, a novel gene encoding the putative RNA-binding Tudor and KH domains [J].
Lamb, FS ;
Barna, TJ ;
Goud, C ;
Marenholz, I ;
Mischke, D ;
Schutte, BC .
GENE, 2000, 246 (1-2) :209-218
[24]   IDENTIFICATION AND CHARACTERIZATION OF A SPINAL MUSCULAR ATROPHY-DETERMINING GENE [J].
LEFEBVRE, S ;
BURGLEN, L ;
REBOULLET, S ;
CLERMONT, O ;
BURLET, P ;
VIOLLET, L ;
BENICHOU, B ;
CRUAUD, C ;
MILLASSEAU, P ;
ZEVIANI, M ;
LEPASLIER, D ;
FREZAL, J ;
COHEN, D ;
WEISSENBACH, J ;
MUNNICH, A ;
MELKI, J .
CELL, 1995, 80 (01) :155-165
[25]   Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression [J].
Mazroui, R ;
Huot, ME ;
Tremblay, S ;
Filion, C ;
Labelle, Y ;
Khandjian, EW .
HUMAN MOLECULAR GENETICS, 2002, 11 (24) :3007-3017
[26]   Inhibition of the ubiquitin-proteasome system induces stress granule formation [J].
Mazroui, Rachid ;
Di Marco, Sergio ;
Kaufman, Randal J. ;
Gallouzi, Imed-Eddine .
MOLECULAR BIOLOGY OF THE CELL, 2007, 18 (07) :2603-2618
[27]   A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs [J].
Meister, G ;
Bühler, D ;
Pillai, R ;
Lottspeich, F ;
Fischer, U .
NATURE CELL BIOLOGY, 2001, 3 (11) :945-949
[28]   SMNrp is an essential pre-mRNA splicing factor required for the formation of the mature spliceosome [J].
Meister, G ;
Hannus, S ;
Plöttner, O ;
Baars, T ;
Hartmann, E ;
Fakan, S ;
Laggerbauer, B ;
Fischer, U .
EMBO JOURNAL, 2001, 20 (09) :2304-2314
[29]   The eIF4G-homolog p97 can activate translation independent of caspase cleavage [J].
Nousch, Marco ;
Reed, Victoria ;
Bryson-Richardson, Robert J. ;
Currie, Peter D. ;
Preiss, Thomas .
RNA, 2007, 13 (03) :374-384
[30]   The pathophysiology of fragile X syndrome [J].
Penagarikano, Olga ;
Mulle, Jennifer G. ;
Warren, Stephen T. .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2007, 8 :109-129