The rRNA-processing function of the yeast U14 small nucleolar RNA can be rescued by a conserved RNA helicase-like protein

被引:68
作者
Liang, WQ
Clark, JA
Fournier, MJ
机构
[1] UNIV MASSACHUSETTS, LEDERLE GRAD RES CTR, DEPT BIOCHEM & MOL BIOL, AMHERST, MA 01003 USA
[2] UNIV MASSACHUSETTS, LEDERLE GRAD RES CTR, MOL & CELLULAR BIOL PROGRAM, AMHERST, MA 01003 USA
关键词
D O I
10.1128/MCB.17.7.4124
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The phylogenetically conserved U14 small nucleolar RNA is required for professing of rRNA, and this function involves base pairing with conserved complementary sequences in 18S RNA. With a view to identifying other important U14 interactions, a stem-loop domain required for activity of Saccharomyces cerevisiae U14 RNAs (the Y domain) was first subjected to detailed mutational analysis, The mapping results showed that most nucleotides of the Y domain can be replaced without affecting function, except for loop nucleotides conserved among five different yeast species. Defective variants were then used to identify both intragenic and extragenic suppressor mutations, All of the intragenic mutations mapped within six nucleotides of the primary mutation, suggesting that suppression involves a change in conformation and that the loop element is involved in an essential intermolecular interaction rather than intramolecular base pairing. A high-copy extragenic suppressor gene, designated DBP4 (DEAD box protein Jj, encodes an essential, putative RNA helicase of the DEAD-DEXH box family. Suppression by DBP4 (initially CA4 [T.-H. Chang, J, Arenas, and J, Abelson, Proc, Natl. Acad. Sci, USA 57:1571-1575, 1990]) restores the level of 18S rRNA and is specific for the Y domain but is not allele specific, DBP4 is predicted to function either in assembly of the U14 small nucleolar RNP or, more likely, in its interaction with other components of the rRNA processing apparatus, Mediating the interaction of U14 with precursor 18S RNA is an especially attractive possibility.
引用
收藏
页码:4124 / 4132
页数:9
相关论文
共 50 条
[1]
RNase III cleaves eukaryotic preribosomal RNA at a U3 snoRNP-dependent site [J].
AbouElela, S ;
Igel, H ;
Ares, M .
CELL, 1996, 85 (01) :115-124
[2]
Ausubel FA, 1995, CURRENT PROTOCOLS MO
[3]
ANTISENSE SNORNAS - A FAMILY OF NUCLEOLAR RNAS WITH LONG COMPLEMENTARITIES TO RIBOSOMAL-RNA [J].
BACHELLERIE, JP ;
MICHOT, B ;
NICOLOSO, M ;
BALAKIN, A ;
NI, JW ;
FOURNIER, MJ .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (07) :261-264
[4]
BALAKIN AG, 1994, J BIOL CHEM, V269, P739
[5]
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
[6]
BASE-PAIRING BETWEEN U3 AND THE PRE-RIBOSOMAL-RNA IS REQUIRED FOR 18S RIBOSOMAL-RNA SYNTHESIS [J].
BELTRAME, M ;
TOLLERVEY, D .
EMBO JOURNAL, 1995, 14 (17) :4350-4356
[7]
2 DIFFERENTIALLY REGULATED MESSENGER-RNAS WITH DIFFERENT 5' ENDS ENCODE SECRETED AND INTRACELLULAR FORMS OF YEAST INVERTASE [J].
CARLSON, M ;
BOTSTEIN, D .
CELL, 1982, 28 (01) :145-154
[8]
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
[9]
IDENTIFICATION OF 5 PUTATIVE YEAST RNA HELICASE GENES [J].
CHANG, TH ;
ARENAS, J ;
ABELSON, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1571-1575
[10]
EICHLER DC, 1994, PROG NUCLEIC ACID RE, V49, P197