Nop53p, an essential nucleolar protein that interacts with Nop17p and Nip7p, is required for pre-rRNA processing in Saccharomyces cerevisiae

被引:31
作者
Granato, DC
Gonzales, FA
Luz, JS
Cassiola, F
Machado-Santelli, GM
Oliveira, CC
机构
[1] Univ Sao Paulo, Inst Quim, Dept Bioquim, BR-05508000 Sao Paulo, Brazil
[2] Univ Sao Paulo, Inst Biomed Sci, Dept Cellular & Dev Biol, Sao Paulo, Brazil
关键词
rRNA processing; nucleolus; ribosome synthesis; Saccharomyces cerevisiae; pre60S;
D O I
10.1111/j.1742-4658.2005.04861.x
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
In eukaryotes, pre-rRNA processing depends on a large number of nonribosomal trans-acting factors that form large and intriguingly organized complexes. A novel nucleolar protein, Nop53p, was isolated by using Nop17p as bait in the yeast two-hybrid system. Nop53p also interacts with a second nucleolar protein, Nip7p. A carbon source-conditional strain with the NOP53 coding sequence under the control of the GAL1 promoter did not grow in glucose-containing medium, showing the phenotype of an essential gene. Under nonpermissive conditions, the conditional mutant strain showed rRNA biosynthesis defects, leading to an accumulation of the 27S and 7S pre-rRNAs and depletion of the mature 25S and 5.8S mature rRNAs. Nop53p did not interact with any of the exosome subunits in the yeast two-hybrid system, but its depletion affects the exosome function. In pull-down assays, protein A-tagged Nop53p coprecipitated the 27S and 7S pre-rRNAs, and His-Nop53p also bound directly 5.8S rRNA in vitro, which is consistent with a role for Nop53p in pre-rRNA processing.
引用
收藏
页码:4450 / 4463
页数:14
相关论文
共 51 条
[1]   Functions of the exosome in rRNA, snoRNA and snRNA synthesis [J].
Allmang, C ;
Kufel, J ;
Chanfreau, G ;
Mitchell, P ;
Petfalski, E ;
Tollervey, D .
EMBO JOURNAL, 1999, 18 (19) :5399-5410
[2]   Degradation of ribosomal RNA precursors by the exosome [J].
Allmang, Christine ;
Mitchell, Philip ;
Petfalski, Elisabeth ;
Tollervey, David .
NUCLEIC ACIDS RESEARCH, 2000, 28 (08) :1684-1691
[3]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[4]   Nucleolar proteome dynamics [J].
Andersen, JS ;
Lam, YW ;
Leung, AKL ;
Ong, SE ;
Lyon, CE ;
Lamond, AI ;
Mann, M .
NATURE, 2005, 433 (7021) :77-83
[5]   Guiding ribose methylation of rRNA [J].
Bachellerie, JP ;
Cavaille, J .
TRENDS IN BIOCHEMICAL SCIENCES, 1997, 22 (07) :257-261
[6]  
BARTEL PL, 1995, METHOD ENZYMOL, V254, P241
[7]   Identification of a 60S preribosomal particle that is closely linked to nuclear export [J].
Bassler, J ;
Grandi, P ;
Gadal, O ;
Lessmann, T ;
Petfalski, E ;
Tollervey, D ;
Lechner, J ;
Hurt, E .
MOLECULAR CELL, 2001, 8 (03) :517-529
[8]   Functional redundancy of Spb1p and a snR52-dependent mechanism for the 2′-O-ribose methylation of a conserved rRNA position in yeast [J].
Bonnerot, C ;
Pintard, L ;
Lutfalla, G .
MOLECULAR CELL, 2003, 12 (05) :1309-1315
[9]   Site-specific cross-linking analyses reveal an asymmetric protein distribution for a box C/D snoRNP [J].
Cahill, NM ;
Friend, K ;
Speckmann, W ;
Li, ZH ;
Terns, RM ;
Terns, MP ;
Steitz, JA .
EMBO JOURNAL, 2002, 21 (14) :3816-3828
[10]   Npa1p, a component of very early pre-60S ribosomal particles, associates with a subset of small nucleolar RNPs required for peptidyl transferase center modification [J].
Dez, C ;
Froment, C ;
Noaillac-Depeyre, J ;
Monsarrat, B ;
Caizergues-Ferrer, M ;
Henry, Y .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (14) :6324-6337