Box H and box ACA are nucleolar localization elements of U17 small nucleolar RNA

被引:37
作者
Lange, TS
Ezrokhi, M
Amaldi, F
Gerbi, SA [1 ]
机构
[1] Brown Univ, Div Biol & Med, Providence, RI 02912 USA
[2] Univ Roma Tor Vergata, Dipartimento Biol, I-00133 Rome, Italy
关键词
D O I
10.1091/mbc.10.11.3877
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The nucleolar localization elements (NoLEs) of U17 small nucleolar RNA (snoRNA), which is essential for rRNA processing and belongs to the box H/ACA snoRNA family, were analyzed by fluorescence microscopy. Injection of mutant U17 transcripts into Xenopus laevis oocyte nuclei revealed that deletion of stems 1, 2, and 4 of U17 snoRNA reduced but did not prevent nucleolar localization. The deletion of stem 3 had no adverse effect. Therefore, the hairpins of the hairpin-hinge-hairpin-tail structure formed by these stems are not absolutely critical for nucleolar localization of U17, nor are sequences within stems 1, 3, and 4, which may tether U17 to the rRNA precursor by base pairing. In contrast, box H and box ACA are major NoLEs; their combined substitution or deletion abolished nucleolar localization of U17 snoRNA. Mutation of just box H or just the box ACA region alone did not fully abolish the nucleolar localization of U17. This indicates that the NoLEs of the box H/ACA snoRNA family function differently from the bipartite NoLEs (conserved boxes C and D) of box C/D snoRNAs, where mutation of either box alone prevents nucleolar localization.
引用
收藏
页码:3877 / 3890
页数:14
相关论文
共 72 条
[1]   The RNA world of the nucleolus: Two major families of small RNAs defined by different box elements with related functions [J].
Balakin, AG ;
Smith, L ;
Fournier, MJ .
CELL, 1996, 86 (05) :823-834
[2]   Nucleolar localization of early tRNA processing [J].
Bertrand, E ;
Houser-Scott, F ;
Kendall, A ;
Singer, RH ;
Engelke, DR .
GENES & DEVELOPMENT, 1998, 12 (16) :2463-2468
[3]   Elements essential for accumulation and function of small nucleolar RNAs directing site-specific pseudouridylation of ribosomal RNAs [J].
Bortolin, ML ;
Ganot, P ;
Kiss, T .
EMBO JOURNAL, 1999, 18 (02) :457-469
[4]   A small nucleolar RNP protein is required for pseudouridylation of eukaryotic ribosomal RNAs [J].
BousquetAntonelli, C ;
Henry, Y ;
Gelugne, JP ;
CaizerguesFerrer, M ;
Kiss, T .
EMBO JOURNAL, 1997, 16 (15) :4770-4776
[5]   The yeast nucleolar protein Cbf5p is involved in rRNA biosynthesis and interacts genetically with the RNA polymerase I transcription factor RRN3 [J].
Cadwell, C ;
Yoon, HJ ;
Zebarjadian, Y ;
Carbon, J .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (10) :6175-6183
[6]   Targeted ribose methylation of RNA in vivo directed by tailored antisense RNA guides [J].
Cavaille, J ;
Nicoloso, M ;
Bachellerie, JP .
NATURE, 1996, 383 (6602) :732-735
[7]   U17(XS8), A SMALL NUCLEOLAR RNA WITH A 12 NT COMPLEMENTARITY TO 18S RIBOSOMAL-RNA AND CODED BY A SEQUENCE REPEATED IN THE 6 INTRONS OF XENOPUS-LAEVIS RIBOSOMAL PROTEIN-S8 GENE [J].
CECCONI, F ;
MARIOTTINI, P ;
LORENI, F ;
PIERANDREIAMALDI, P ;
CAMPIONI, N ;
AMALDI, F .
NUCLEIC ACIDS RESEARCH, 1994, 22 (05) :732-741
[8]   THE XENOPUS INTRON-ENCODED U17 SNORNA IS PRODUCED BY EXONUCLEOLYTIC PROCESSING OF ITS PRECURSOR IN OOCYTES [J].
CECCONI, F ;
MARIOTTINI, P ;
AMALDI, F .
NUCLEIC ACIDS RESEARCH, 1995, 23 (22) :4670-4676
[9]   A functional role for some Fugu introns larger than the typical short ones: The example of the gene coding for ribosomal protein S7 and snoRNA U17 [J].
Cecconi, F ;
Crosio, C ;
Mariottini, P ;
Cesareni, G ;
Giorgi, M ;
Brenner, S ;
Amaldi, F .
NUCLEIC ACIDS RESEARCH, 1996, 24 (16) :3167-3172
[10]   THE RNA OF RNASE MRP IS REQUIRED FOR NORMAL PROCESSING OF RIBOSOMAL-RNA [J].
CHU, S ;
ARCHER, RH ;
ZENGEL, JM ;
LINDAHL, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) :659-663