A common motif organizes the structure of multi-helix loops in 16 S and 23 S ribosomal RNAs

被引:155
作者
Leontis, NB
Westhof, E
机构
[1] CNRS, Inst Biol Mol & Cellulaire, UPR 9002, F-67084 Strasbourg, France
[2] Bowling Green State Univ, Dept Chem, Bowling Green, OH 43403 USA
关键词
RNA; multi-helix loops; recurrent motif; phylogenetic analysis;
D O I
10.1006/jmbi.1998.2106
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
Phylogenetic and chemical probing data indicate that a modular RNA motif, common to loop E of eucaryotic 5 S ribosomal RNA (rRNA) and the alpha-sarcin/ricin loop of 23 S rRNA, organizes the structure of multi-helix loops in 16 S and 23 S ribosomal RNAs. The motif occurs in the 3' domain of 16 S rRNA at positions 1345-1350/1372-1376 (Escherichia coli numbering), within the three-way junction loop, which binds ribosomal protein S7, and which contains nucleotides that help to form the binding site for P-site tRNA in the ribosome. The motif also helps to structure a three-way junction within domain I of 23 S, which contains many universally conserved bases and which lies close in the primary and secondary structure to the binding site of r-protein L24. Several other highly conserved hairpin, internal, and multi-helix loops in 16 S and 23 S rRNA contain the motif, including the core junction loop of 23 S and helix 27 in the core of 16 S rRNA. Sequence conservation and range of variation in bacteria, archaea, and eucaryotes as well as chemical probing and crosslinking data, provide support for the recurrent and autonomous existence of the motif in ribosomal RNAs. Besides its presence in the hairpin ribozyme, the loop E motif is also apparent in helix P10 of bacterial RNase P, in domain P7 of one sub-group of group I introns, and in domain 3 of one subgroup of group II introns. (C) 1998 Academic Press.
引用
收藏
页码:571 / 583
页数:13
相关论文
共 69 条
[1]   REQUIREMENT FOR A CONSERVED, TERTIARY INTERACTION IN THE CORE OF 23S RIBOSOMAL-RNA [J].
AAGAARD, C ;
DOUTHWAITE, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (08) :2989-2993
[2]   RNA PROTEIN INTERACTIONS OF STORED 5S-RNA WITH TFIIIA AND RIBOSOMAL PROTEIN-L5 DURING XENOPUS-OOGENESIS [J].
ALLISON, LA ;
ROMANIUK, PJ ;
BAKKEN, AH .
DEVELOPMENTAL BIOLOGY, 1991, 144 (01) :129-144
[3]   HIGHER-ORDER STRUCTURE OF DOMAIN-III IN ESCHERICHIA-COLI 16S RIBOSOMAL-RNA, 30S SUBUNIT AND 70S RIBOSOME [J].
BAUDIN, F ;
EHRESMANN, C ;
ROMBY, P ;
MOUGEL, M ;
COLIN, J ;
LEMPEREUR, L ;
BACHELLERIE, JP ;
EBEL, JP ;
EHRESMANN, B .
BIOCHIMIE, 1987, 69 (10) :1081-1096
[4]   Viroid processing: Switch from cleavage to ligation is driven by a change from a tetraloop to a loop E conformation [J].
Baumstark, T ;
Schroder, ARW ;
Riesner, D .
EMBO JOURNAL, 1997, 16 (03) :599-610
[5]   ULTRAVIOLET LIGHT-INDUCED CROSSLINKING REVEALS A UNIQUE REGION OF LOCAL TERTIARY STRUCTURE IN POTATO SPINDLE TUBER VIROID AND HELA 5S RNA [J].
BRANCH, AD ;
BENENFELD, BJ ;
ROBERTSON, HD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (19) :6590-6594
[6]   RNA-PROTEIN INTERACTIONS IN THE ESCHERICHIA-COLI RIBOSOME [J].
BRIMACOMBE, R .
BIOCHIMIE, 1991, 73 (7-8) :927-936
[7]   Hairpin ribozyme: Current status and future prospects [J].
Burke, JM .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1996, 24 (03) :608-615
[8]  
BURKE JM, 1996, NUCL ACIDS MOL BIOL, V10, P129
[9]   A PHOTO-CROSS-LINKABLE TERTIARY STRUCTURE MOTIF FOUND IN FUNCTIONALLY DISTINCT RNA MOLECULES IS ESSENTIAL FOR CATALYTIC FUNCTION OF THE HAIRPIN RIBOZYME [J].
BUTCHER, SE ;
BURKE, JM .
BIOCHEMISTRY, 1994, 33 (04) :992-999
[10]   STRUCTURE-MAPPING OF THE HAIRPIN RIBOZYME - MAGNESIUM-DEPENDENT FOLDING AND EVIDENCE FOR TERTIARY INTERACTIONS WITHIN THE RIBOZYME-SUBSTRATE COMPLEX [J].
BUTCHER, SE ;
BURKE, JM .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 244 (01) :52-63