Literature DB >> 2449656

Evidence for tertiary structure in natural single stranded RNAs in solution.

S Ghribi1, M C Maurel, M Rougee, A Favre.   

Abstract

Binding isotherms (20 degrees C) of ethidium bromide to a number of tRNA species at various ionic strengths indicate that i) the number ni of intercalation sites is high 7 to 11 per molecule, in the low salt form III, but small, 2 to 1, at high Mg2+ or Na+ when form I predominates. ii) modification of tRNA at strategic positions for 3D folding prevents full expression of intercalation restriction iii) maximal restriction is obtained at salt concentrations higher than needed for full conversion to form I. It is inferred that restriction, which is not observed with bihelical RNA (or DNA), requires the native tRNA 3D structure but also some physical coupling between the region of 3D folding and bihelical arms. Ribosomal RNAs, some viral RNAs, mRNA from sheep mammary gland as well as the random copolymers Poly UG, Poly AUG, Poly AUCG all exhibit intercalation restriction. Hence 3D folding of the polyribonucleotide chains appears to be a feature common to single-stranded RNAs when free in solution under physiological conditions.

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Year:  1988        PMID: 2449656      PMCID: PMC334739          DOI: 10.1093/nar/16.3.1095

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  23 in total

1.  Lack of poly(A) sequence in half of the messenger RNA coding for ewe alpha S casein.

Authors:  L M Houdebine; P Gaye; A Favre
Journal:  Nucleic Acids Res       Date:  1974-03       Impact factor: 16.971

2.  Introduction of an intramolecular flourescent pobe in E. coli tRNA(Val)(1).

Authors:  A Favre; M Yaniv
Journal:  FEBS Lett       Date:  1971-10-01       Impact factor: 4.124

3.  Secondary structures formed by random RNA sequences.

Authors:  B Ricard; W Salser
Journal:  Biochem Biophys Res Commun       Date:  1975-04-07       Impact factor: 3.575

4.  Studies on secondary structure of single-stranded RNA from bacteriophage MS2 by electron microscopy.

Authors:  A B Jacobson
Journal:  Proc Natl Acad Sci U S A       Date:  1976-02       Impact factor: 11.205

5.  Assignment of the low-field 1H NMR spectrum of Escherichia coli tRNAPhe using nuclear Overhauser effects.

Authors:  E I Hyde; B R Reid
Journal:  Biochemistry       Date:  1985-07-30       Impact factor: 3.162

Review 6.  tRNA-like structures in the genomes of RNA viruses.

Authors:  A L Haenni; S Joshi; F Chapeville
Journal:  Prog Nucleic Acid Res Mol Biol       Date:  1982

7.  Arrangement of protein subunits and the distribution of nucleic acid in turnip yellow mosaic virus. II. Electron microscopic studies.

Authors:  J T Finch; A Klug
Journal:  J Mol Biol       Date:  1966-01       Impact factor: 5.469

8.  Role of divalent ions in folding of tRNA.

Authors:  J L Leroy; M Guéron; G Thomas; A Favre
Journal:  Eur J Biochem       Date:  1977-04-15

9.  Allosteric interpretation of Mg2+ binding to the denaturable Escherichia coli tRNAGlu2+.

Authors:  M Bina-Stein; A Stein
Journal:  Biochemistry       Date:  1976-09-07       Impact factor: 3.162

10.  Three-dimensional structural model of eubacterial 5S RNA that has functional implications.

Authors:  T Pieler; V A Erdmann
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

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  1 in total

1.  Polyadenylation and degradation of structurally abnormal mitochondrial tRNAs in human cells.

Authors:  Marina Toompuu; Tea Tuomela; Pia Laine; Lars Paulin; Eric Dufour; Howard T Jacobs
Journal:  Nucleic Acids Res       Date:  2018-06-01       Impact factor: 16.971

  1 in total

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