tRNA prefers to kiss

Six RNA aptamers that bind to yeast phenylalanine tRNA were identified by in vitro selection from a random‐sequence pool. The two most abundantly represented aptamers interact with the tRNA anticodon loop, each through a sequence block with perfect Watson–Crick complementarity to the loop. It was possible to truncate one of these aptamers to a simple hairpin loop that forms a classical ‘kissing complex’ with the anticodon loop. Three other aptamers have nearly complete complementarity to the anticodon loop. The sixth aptamer has two sequence blocks, one complementary to the tRNA T loop and the other to the D loop; this aptamer binds better to a mutant tRNA that disrupts the normal D‐loop/T‐loop tertiary interaction than to the wild‐type tRNA. Selection of complements to tRNA loops occurred despite an attempt to direct binding to tertiary structural features of tRNA. This serves as a reminder of how special the RNA–RNA interactions are that are not based on complementarity. Nonetheless, these aptamers must present the tRNA complement in some special structural context; the simple single‐strand complement of the anticodon loop did not bind tRNA effectively.

[1]  S A Benner,et al.  Modern metabolism as a palimpsest of the RNA world. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[2]  D. Crothers,et al.  Determinants of RNA hairpin loop-loop complex stability. , 1995, Journal of molecular biology.

[3]  H. Heus,et al.  A network of heterogeneous hydrogen bonds in GNRA tetraloops. , 1996, Journal of molecular biology.

[4]  Andrew D. Ellington,et al.  genetic analysis: Selection and amplification of rare functional nucleic acids , 1991 .

[5]  I. Majerfeld,et al.  Affinity selection-amplification from randomized ribooligonucleotide pools. , 1996, Methods in enzymology.

[6]  I. Tinoco,et al.  Mapping of a protein-RNA kissing hairpin interface: Rom and Tar-Tar*. , 1998, Nucleic acids research.

[7]  Solution studies of the dimerization initiation site of HIV-1 genomic RNA. , 1998, Nucleic acids research.

[8]  F. Michel,et al.  Rules for RNA recognition of GNRA tetraloops deduced by in vitro selection: comparison with in vivo evolution , 1997, The EMBO journal.

[9]  L E Orgel,et al.  RNA catalysis and the origins of life. , 1986, Journal of theoretical biology.

[10]  M. Nomura,et al.  Activity of ribosomes containing 5S RNA with a chemically modified 3'-terminus. , 1972, Proceedings of the National Academy of Sciences of the United States of America.

[11]  D. Turner,et al.  Solution structure of (rGCGGACGC)2 by two-dimensional NMR and the iterative relaxation matrix approach. , 1996, Biochemistry.

[12]  I. Tinoco,et al.  The structure of an RNA "kissing" hairpin complex of the HIV TAR hairpin loop and its complement. , 1997, Journal of molecular biology.

[13]  D. Turner,et al.  Structure of (rGGCGAGCC)2 in solution from NMR and restrained molecular dynamics. , 1993, Biochemistry.

[14]  D. Labuda,et al.  Mechanism of codon recognition by transfer RNA studied with oligonucleotides larger than triplets. , 1985, Nucleic acids research.

[15]  R. Green,et al.  In vitro genetic analysis of the hinge region between helical elements P5-P4-P6 and P7-P3-P8 in the sunY group I self-splicing intron. , 1994, Journal of molecular biology.

[16]  C. Cantor,et al.  Fluorescence studies of the binding of a yeast tRNAPhe derivative to Escherichia coli ribosomes. , 1979, Journal of molecular biology.

[17]  S. Altman,et al.  Substrate recognition by human RNase P: identification of small, model substrates for the enzyme. , 1995, The EMBO journal.

[18]  S. Strobel,et al.  A minor groove RNA triple helix within the catalytic core of a group I intron , 1998, Nature Structural Biology.

[19]  G. Tocchini-Valentini,et al.  Two helices plus a linker: a small model substrate for eukaryotic RNase P. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[20]  K. Flaherty,et al.  Three-dimensional structure of a hammerhead ribozyme , 1994, Nature.

[21]  Selection of novel forms of a functional domain within the Tetrahymena ribozyme. , 1994, Nucleic acids research.

[22]  Sung-Hou Kim Crystal Structure of Yeast tRNA phe and General Structural Features of Other tRNAs , 1979 .

[23]  V. M. Reyes,et al.  A synthetic substrate for tRNA splicing. , 1987, Analytical biochemistry.

[24]  J W Szostak,et al.  Selection of a ribozyme that functions as a superior template in a self-copying reaction. , 1992, Science.

[25]  H. Nicholas,et al.  Interacting RNA species identified by combinatorial selection. , 1997, Bioorganic & medicinal chemistry.

[26]  D. Turner,et al.  Solution structure of (rGGCAGGCC)2 by two-dimensional NMR and the iterative relaxation matrix approach. , 1996, Biochemistry.

[27]  S R Holbrook,et al.  A curved RNA helix incorporating an internal loop with G.A and A.A non-Watson-Crick base pairing. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[28]  E. Westhof,et al.  Anticodon-anticodon interaction induces conformational changes in tRNA: yeast tRNAAsp, a model for tRNA-mRNA recognition. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[29]  W. Wintermeyer,et al.  Interactions of yeast tRNAPhe with ribosomes from yeast and Escherichia coli. A fluorescence spectroscopic study. , 1977, European journal of biochemistry.

[30]  O. Uhlenbeck,et al.  Structure of an unmodified tRNA molecule. , 1989, Biochemistry.

[31]  F. Barré-Sinoussi,et al.  HIV‐1 reverse transcriptase specifically interacts with the anticodon domain of its cognate primer tRNA. , 1989, The EMBO journal.

[32]  H. Burrell,et al.  Binding of ribosomal proteins to RNA covalently coupled to agarose. , 1977, European journal of biochemistry.

[33]  A. Klug,et al.  The crystal structure of an AII-RNAhammerhead ribozyme: A proposed mechanism for RNA catalytic cleavage , 1995, Cell.

[34]  J. Tomizawa,et al.  Complexes formed by complementary RNA stem-loops. Their formations, structures and interaction with ColE1 Rom protein. , 1991, Journal of molecular biology.

[35]  Thomas L. James,et al.  Structure of the dimer a initiation complex of HIV-1 genomic RNA , 1998, Nature Structural Biology.

[36]  M. Zuker On finding all suboptimal foldings of an RNA molecule. , 1989, Science.

[37]  J. Doudna,et al.  RNA structure, not sequence, determines the 5' splice-site specificity of a group I intron. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[38]  S Cusack,et al.  The 2.9 A crystal structure of T. thermophilus seryl-tRNA synthetase complexed with tRNA(Ser). , 1994, Science.

[39]  D. Crothers,et al.  Studies of the complex between transfer RNAs with complementary anticodons. I. Origins of enhanced affinity between complementary triplets. , 1976, Journal of molecular biology.

[40]  O. Uhlenbeck,et al.  In vitro selection of RNAs that undergo autolytic cleavage with Pb2+. , 1992, Biochemistry.

[41]  O. Uhlenbeck,et al.  Oligoribonucleotide synthesis using T7 RNA polymerase and synthetic DNA templates. , 1987, Nucleic acids research.

[42]  D. Crothers,et al.  The solution structure of an RNA loop-loop complex: the ColE1 inverted loop sequence. , 1998, Structure.

[43]  B. Ganem RNA world , 1987, Nature.

[44]  J. Puglisi,et al.  HIV-1 A-rich RNA loop mimics the tRNA anticodon structure , 1998, Nature Structural Biology.

[45]  K. M. Harrington,et al.  In vitro analysis of translational rate and accuracy with an unmodified tRNA. , 1993, Biochemistry.

[46]  M Yarus,et al.  Three small ribooligonucleotides with specific arginine sites. , 1993, Biochemistry.