NUCLEOSIDE TRIPLES FROM THE GROUP-I INTRON

被引:33
作者
CHASTAIN, M
TINOCO, I
机构
[1] UNIV CALIF BERKELEY,DEPT CHEM,BERKELEY,CA 94720
[2] UNIV CALIF BERKELEY,CHEM BIODYNAM LAB,BERKELEY,CA 94720
关键词
D O I
10.1021/bi00214a022
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
Oligonucleotides modeled on a proposed base-triple domain in the P4/P6 region of the self-splicing group I intron have been characterized by NMR. The NMR data indicate that single-stranded nucleotides in this domain are in the minor groove of an adjacent helix within hydrogen bonding distance of 2'-hydroxyl groups in an interaction we term a nucleoside triple. Oligonucleotides containing the two most frequently occurring sequences among group I introns in the P4/P6 region formed nucleoside triples in the minor groove, whereas oligonucleotides containing sequences which are not conserved did not form triples. Surprisingly, the structures of the nucleosides triples in the oligonucleotides containing the two most frequently occurring sequences are different. If this difference were maintained in the context of the whole intron, it would suggest that the triples are not directly involved in catalysis, but rather that the nucleoside triples function by aligning the helical domains within the catalytic core of the intron.
引用
收藏
页码:14220 / 14228
页数:9
相关论文
共 23 条
  • [1] PREPARATION OF ISOTOPICALLY LABELED RIBONUCLEOTIDES FOR MULTIDIMENSIONAL NMR-SPECTROSCOPY OF RNA
    BATEY, RT
    INADA, M
    KUJAWINSKI, E
    PUGLISI, JD
    WILLIAMSON, JR
    [J]. NUCLEIC ACIDS RESEARCH, 1992, 20 (17) : 4515 - 4523
  • [2] BRUNGER A, 1990, X PLOR SYSTEM CRYSTA
  • [3] A BASE-TRIPLE STRUCTURAL DOMAIN IN RNA
    CHASTAIN, M
    TINOCO, I
    [J]. BIOCHEMISTRY, 1992, 31 (51) : 12733 - 12741
  • [4] MUTATIONAL ANALYSIS OF CONSERVED NUCLEOTIDES IN A SELF-SPLICING GROUP-I INTRON
    COUTURE, S
    ELLINGTON, AD
    GERBER, AS
    CHERRY, JM
    DOUDNA, JA
    GREEN, R
    HANNA, M
    PACE, U
    RAJAGOPAL, J
    SZOSTAK, JW
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) : 345 - 358
  • [5] SEQUENCE SPECIFICITY OF THE P6 PAIRING FOR SPLICING OF THE GROUP-I TD INTRON OF PHAGE-T4
    EHRENMAN, K
    SCHROEDER, R
    CHANDRY, PS
    HALL, DH
    BELFORT, M
    [J]. NUCLEIC ACIDS RESEARCH, 1989, 17 (22) : 9147 - 9163
  • [6] A TYROSYL TRANSFER-RNA SYNTHETASE BINDS SPECIFICALLY TO THE GROUP-I INTRON CATALYTIC CORE
    GUO, QB
    LAMBOWITZ, AM
    [J]. GENES & DEVELOPMENT, 1992, 6 (08) : 1357 - 1372
  • [7] STRUCTURAL FEATURES THAT GIVE RISE TO THE UNUSUAL STABILITY OF RNA HAIRPINS CONTAINING GNRA LOOPS
    HEUS, HA
    PARDI, A
    [J]. SCIENCE, 1991, 253 (5016) : 191 - 194
  • [8] CRYSTAL-STRUCTURE OF YEAST PHENYLALANINE TRANSFER-RNA .2. STRUCTURAL FEATURES AND FUNCTIONAL IMPLICATIONS
    HOLBROOK, SR
    SUSSMAN, JL
    WARRANT, RW
    KIM, SH
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1978, 123 (04) : 631 - 660
  • [9] SEPARATION AND SUPPRESSION OF COHERENT TRANSFER EFFECTS IN TWO-DIMENSIONAL NOE AND CHEMICAL-EXCHANGE SPECTROSCOPY
    MACURA, S
    WUTHRICH, K
    ERNST, RR
    [J]. JOURNAL OF MAGNETIC RESONANCE, 1982, 46 (02) : 269 - 282
  • [10] APPLICATION OF PHASE SENSITIVE TWO-DIMENSIONAL CORRELATED SPECTROSCOPY (COSY) FOR MEASUREMENTS OF H-1-H-1 SPIN-SPIN COUPLING-CONSTANTS IN PROTEINS
    MARION, D
    WUTHRICH, K
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1983, 113 (03) : 967 - 974