A novel acidophilic RNA motif that recognizes coenzyme A

被引:36
作者
Burke, DH [1 ]
Hoffman, DC [1 ]
机构
[1] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
关键词
D O I
10.1021/bi972877p
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
Specific recognition of nucleotide cofactors by RNA may be important in engineering new RNA enzymes (ribozymes). Although in vitro selections (SELEX) have identified nucleic acid motifs ("aptamers") that bind a variety of adenosine cofactors, none of these recognizes coenzyme A (CoA), the primary biological cofactor used in acyltransfer reactions. We used SELEX experiments with two random RNA pools to identify aptamers that bind CoA. Functional boundary determination and extensive comparative sequence analysis (including reselection of a mutagenized, circularly permuted RNA) led to the identification of a 52 nucleotide minimal aptamer ("min52"). The RNA structural motif contains a large internal loop with 26 unpaired nucleotides flanked by helices of any base-paired sequence. Twenty loop nucleotides are specifically required for binding activity, 12 of which are derived from the original primer binding sequences. Specificity studies with CoA analogues demonstrated that the aptamer recognizes many adenosine analogues, including ATP, and that recognition is predominantly through the Hoogsteen face of adenine. Binding activity is greatest at acidic pH (optimum near 5.0), in low or no monovalent salt, and at high concentrations of either Mg2+ or Mn2+. Strong binding activity (86% of maximum) is observed at pH 4.0, suggesting that at least some extreme conditions (acidic pH) may be compatible with RNA World theories of the origin and early evolution of life. In the presence of 10 mM Mg2+, binding is unaffected by the addition of 1 mM Ca2+, but it is mildly inhibited by 1 mM Zn2+ or Co2+ or by 0.1 mM Cu2+ or Ni2+. The dissociation constant (K-d) for the association of min52 RNA with ATP in solution was measured to be 2.4 +/- 0.4 mu M under the conditions of the selection and 0.5 +/- 0.1 mu M under optimized conditions. Finally, we show that the selected CoA aptamer populations contain other RNAs at low frequencies that preferentially recognize intact CoA and are not eluted from the resin by AMP alone.
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收藏
页码:4653 / 4663
页数:11
相关论文
共 49 条
  • [1] DIRECTED EVOLUTION OF AN RNA ENZYME
    BEAUDRY, AA
    JOYCE, GF
    [J]. SCIENCE, 1992, 257 (5070) : 635 - 641
  • [2] MODERN METABOLISM AS A PALIMPSEST OF THE RNA WORLD
    BENNER, SA
    ELLINGTON, AD
    TAUER, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (18) : 7054 - 7058
  • [3] BENNER SA, 1993, RNA WORLD, P27
  • [4] RNA LIGANDS TO HUMAN NERVE GROWTH-FACTOR
    BINKLEY, J
    ALLEN, P
    BROWN, DM
    GREEN, L
    TUERK, C
    GOLD, L
    [J]. NUCLEIC ACIDS RESEARCH, 1995, 23 (16) : 3198 - 3205
  • [5] ISOLATION OF RNA APTAMERS FOR BIOLOGICAL COFACTORS BY IN-VITRO SELECTION
    BURGSTALLER, P
    FAMULOK, M
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1994, 33 (10): : 1084 - 1087
  • [6] Bent pseudoknots and novel RNA inhibitors of type 1 human immunodeficiency virus (HIV-1) reverse transcriptase
    Burke, DH
    Scates, L
    Andrews, K
    Gold, L
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1996, 264 (04) : 650 - 666
  • [7] RNA aptamers to the adenosine moiety of S-adenosyl methionine: structural inferences from variations on a theme and the reproducibility of SELEX
    Burke, DH
    Gold, L
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (10) : 2020 - 2024
  • [8] RNA aptamers to the peptidyl transferase inhibitor chloramphenicol
    Burke, DH
    Hoffman, DC
    Brown, A
    Hansen, M
    Pardi, A
    Gold, L
    [J]. CHEMISTRY & BIOLOGY, 1997, 4 (11): : 833 - 843
  • [9] 3 SMALL RIBOOLIGONUCLEOTIDES WITH SPECIFIC ARGININE SITES
    CONNELL, GJ
    ILLANGESEKARE, M
    YARUS, M
    [J]. BIOCHEMISTRY, 1993, 32 (21) : 5497 - 5502
  • [10] ORIGIN OF GENETIC CODE
    CRICK, FHC
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1968, 38 (03) : 367 - &