The essential WD-repeat protein Rsa4p is required for rRNA processing and intra-nuclear transport of 60S ribosomal subunits

被引:42
作者
de la Cruz, J
Sanz-Martínez, E
Remacha, M
机构
[1] Univ Seville, Fac Biol, Dept Genet, E-41012 Seville, Spain
[2] CSIC, Ctr Biol Mol Severo Ochoa, E-28049 Madrid, Spain
[3] Univ Autonoma Madrid, E-28049 Madrid, Spain
关键词
D O I
10.1093/nar/gki887
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
We report the characterization of a novel factor, Rsa4p (Ycr072cp), which is essential for the synthesis of 60S ribosomal subunits. Rsa4p is a conserved WD-repeat protein that seems to localize in the nucleolus. In vivo depletion of Rsa4p results in a deficit of 60S ribosomal subunits and the appearance of half-mer polysomes. Northern hybridization and primer extension analyses of pre-rRNA and mature rRNAs show that depletion of Rsa4p leads to the accumulation of the 27S, 25.5S and 7S pre-rRNAs, resulting in a reduction of the mature 25S and 5.8S rRNAs. Pulse-chase analyses of pre-rRNA processing reveal that, at least, this is due to a strong delay in the maturation of 27S pre-rRNA intermediates to mature 25S rRNA. Furthermore, depletion of Rsa4p inhibited the release of the pre-60S ribosomal particles from the nucleolus to the nucleoplasm, as judged by the predominantly nucleolar accumulation of the large subunit Rpl25-eGFP reporter construct. We propose that Rsa4p associates early with pre-60S ribosomal particles and provides a platform of interaction for correct processing of rRNA precursors and nucleolar release of 60S ribosomal subunits.
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收藏
页码:5728 / 5739
页数:12
相关论文
共 62 条
[31]   The putative GTPases Nog1p and Lsg1p are required for 60S ribosomal subunit biogenesis and are localized to the nucleus and cytoplasm, respectively [J].
Kallstrom, G ;
Hedges, J ;
Johnson, A .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (12) :4344-4355
[32]   GRC5 and NMD3 function in translational control of gene expression and interact genetically [J].
Karl, T ;
Önder, K ;
Kodzius, R ;
Pichová, A ;
Wimmer, H ;
Thür, A ;
Hundsberger, H ;
Löffler, M ;
Klade, T ;
Beyer, A ;
Breitenbach, M ;
Koller, L .
CURRENT GENETICS, 1999, 34 (06) :419-429
[33]   High-definition macromolecular composition of yeast RNA-processing complexes [J].
Krogan, NJ ;
Peng, WT ;
Cagney, G ;
Robinson, MD ;
Haw, R ;
Zhong, GQ ;
Guo, XH ;
Zhang, X ;
Canadien, V ;
Richards, DP ;
Beattie, BK ;
Lalev, A ;
Zhang, W ;
Davierwala, AP ;
Mnaimneh, S ;
Starostine, A ;
Tikuisis, AP ;
Grigull, J ;
Datta, N ;
Bray, JE ;
Hughes, TR ;
Emili, A ;
Greenblatt, JF .
MOLECULAR CELL, 2004, 13 (02) :225-239
[34]   A noc complex specifically involved in the formation and nuclear export of ribosomal 40 S subunits [J].
Milkereit, P ;
Strauss, D ;
Bassler, J ;
Gadal, O ;
Kühn, H ;
Schütz, S ;
Gas, N ;
Lechner, J ;
Hurt, E ;
Tschochner, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (06) :4072-4081
[35]   Maturation and intranuclear transport of pre-ribosomes requires Noc proteins [J].
Milkereit, P ;
Gadal, O ;
Podtelejnikov, A ;
Trumtel, S ;
Gas, N ;
Petfalski, E ;
Tollervey, D ;
Mann, M ;
Hurt, E ;
Tschochner, H .
CELL, 2001, 105 (04) :499-509
[36]   60S pre-ribosome formation viewed from assembly in the nucleolus until export to the cytoplasm [J].
Nissan, TA ;
Bassler, J ;
Petfalski, E ;
Tollervey, D ;
Hurt, E .
EMBO JOURNAL, 2002, 21 (20) :5539-5547
[37]   A pre-ribosome-associated HEAT-repeat protein is required for export of both ribosomal subunits [J].
Oeffinger, M ;
Dlakic, M ;
Tollervey, D .
GENES & DEVELOPMENT, 2004, 18 (02) :196-209
[38]   Yeast Pescadillo is required for multiple activities during 60S ribosomal subunit synthesis [J].
Oeffinger, M ;
Lueng, A ;
Lamond, A ;
Tollervey, D .
RNA, 2002, 8 (05) :626-636
[39]   The WD-repeat protein Pfs2p bridges two essential factors within the yeast pre-mRNA 3′-end-processing complex [J].
Ohnacker, M ;
Barabino, SML ;
Preker, PJ ;
Keller, W .
EMBO JOURNAL, 2000, 19 (01) :37-47
[40]   THE COMPLETE DNA-SEQUENCE OF YEAST CHROMOSOME-III [J].
OLIVER, SG ;
VANDERAART, QJM ;
AGOSTONI-CARBONE, ML ;
AIGLE, M ;
ALBERGHINA, L ;
ALEXANDRAKI, D ;
ANTOINE, G ;
ANWAR, R ;
BALLESTA, JPG ;
BENIT, P ;
BERBEN, G ;
BERGANTINO, E ;
BITEAU, N ;
BOLLE, PA ;
BOLOTINFUKUHARA, M ;
BROWN, A ;
BROWN, AJP ;
BUHLER, JM ;
CARCANO, C ;
CARIGNANI, G ;
CEDERBERG, H ;
CHANET, R ;
CONTRERAS, R ;
CROUZET, M ;
DAIGNANFORNIER, B ;
DEFOOR, E ;
DELGADO, M ;
DEMOLDER, J ;
DOIRA, C ;
DUBOIS, E ;
DUJON, B ;
DUSTERHOFT, A ;
ERDMANN, D ;
ESTEBAN, M ;
FABRE, F ;
FAIRHEAD, C ;
FAYE, G ;
FELDMANN, H ;
FIERS, W ;
FRANCINGUESGAILLARD, MC ;
FRANCO, L ;
FRONTALI, L ;
FUKUHARA, H ;
FULLER, LJ ;
GALLAND, P ;
GENT, ME ;
GIGOT, D ;
GILLIQUET, V ;
GLANSDORFF, N ;
GOFFEAU, A .
NATURE, 1992, 357 (6373) :38-46