Literature DB >> 7544890

Use of ultra stable UNCG tetraloop hairpins to fold RNA structures: thermodynamic and spectroscopic applications.

M Molinaro1, I Tinoco.   

Abstract

RNA molecules of > 20 nucleotides have been the focus of numerous recent NMR structural studies. Several investigators have used the UNCG family of hairpins to ensure proper folding. We show that th UUCG hairpin has a minimum requirement of a two base-pair stem. Hairpins with a CG loop closing base pair and an initial 5'CG or 5'GC base pair have a melting temperature approximately 55 degrees C in 10 mM sodium phosphate. The high stability of even such small hairpins suggests that the hairpin can serve as a nucleation site for folding. For high resolution NMR work, the UNCG loop family (UACG in particular) provides excellent spectroscopic markers in one-dimensional exchangeable spectra, in two-dimensional COSY spectra and in NOESY spectra that clearly define it as forming a hairpin. This allows straightforward initiation of chemical shift assignments.

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Year:  1995        PMID: 7544890      PMCID: PMC307149          DOI: 10.1093/nar/23.15.3056

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


  21 in total

1.  Extraordinarily stable mini-hairpins: electrophoretical and thermal properties of the various sequence variants of d(GCGAAAGC) and their effect on DNA sequencing.

Authors:  I Hirao; Y Nishimura; Y Tagawa; K Watanabe; K Miura
Journal:  Nucleic Acids Res       Date:  1992-08-11       Impact factor: 16.971

2.  Synthesis and purification of large amounts of RNA oligonucleotides.

Authors:  J R Wyatt; M Chastain; J D Puglisi
Journal:  Biotechniques       Date:  1991-12       Impact factor: 1.993

3.  Distinguishing between duplex and hairpin forms of RNA by 15N-1H heteronuclear NMR.

Authors:  F Aboul-ela; E P Nikonowicz; A Pardi
Journal:  FEBS Lett       Date:  1994-06-27       Impact factor: 4.124

4.  The conformation of loop E of eukaryotic 5S ribosomal RNA.

Authors:  B Wimberly; G Varani; I Tinoco
Journal:  Biochemistry       Date:  1993-02-02       Impact factor: 3.162

5.  The conformation of the sarcin/ricin loop from 28S ribosomal RNA.

Authors:  A A Szewczak; P B Moore; Y L Chang; I G Wool
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

6.  Inhibition of c-Ha-ras gene expression by hammerhead ribozymes containing a stable C(UUCG)G hairpin loop.

Authors:  M Koizumi; H Kamiya; E Ohtsuka
Journal:  Biol Pharm Bull       Date:  1993-09       Impact factor: 2.233

7.  Binding of an HIV Rev peptide to Rev responsive element RNA induces formation of purine-purine base pairs.

Authors:  J L Battiste; R Tan; A D Frankel; J R Williamson
Journal:  Biochemistry       Date:  1994-03-15       Impact factor: 3.162

8.  1H NMR studies of the high-affinity Rev binding site of the Rev responsive element of HIV-1 mRNA: base pairing in the core binding element.

Authors:  R D Peterson; D P Bartel; J W Szostak; S J Horvath; J Feigon
Journal:  Biochemistry       Date:  1994-05-10       Impact factor: 3.162

9.  Contributions of dangling end stacking and terminal base-pair formation to the stabilities of XGGCCp, XCCGGp, XGGCCYp, and XCCGGYp helixes.

Authors:  S M Freier; D Alkema; A Sinclair; T Neilson; D H Turner
Journal:  Biochemistry       Date:  1985-08-13       Impact factor: 3.162

10.  The nature of preferred hairpin structures in 16S-like rRNA variable regions.

Authors:  J Wolters
Journal:  Nucleic Acids Res       Date:  1992-04-25       Impact factor: 16.971

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  38 in total

1.  Thermodynamics of 2'-ribose substitutions in UUCG tetraloops.

Authors:  D J Williams; J L Boots; K B Hall
Journal:  RNA       Date:  2001-01       Impact factor: 4.942

2.  A ribozyme selected from variants of U6 snRNA promotes 2',5'-branch formation.

Authors:  T Tuschl; P A Sharp; D P Bartel
Journal:  RNA       Date:  2001-01       Impact factor: 4.942

3.  Polyvalent Rev decoys act as artificial Rev-responsive elements.

Authors:  T L Symensma; S Baskerville; A Yan; A D Ellington
Journal:  J Virol       Date:  1999-05       Impact factor: 5.103

4.  Solution structure of the pseudo-5' splice site of a retroviral splicing suppressor.

Authors:  Javier Cabello-Villegas; Keith E Giles; Ana Maria Soto; Ping Yu; Annie Mougin; Karen L Beemon; Yun-Xing Wang
Journal:  RNA       Date:  2004-09       Impact factor: 4.942

5.  Natural selection is not required to explain universal compositional patterns in rRNA secondary structure categories.

Authors:  Sandra Smit; Michael Yarus; Rob Knight
Journal:  RNA       Date:  2006-01       Impact factor: 4.942

Review 6.  Recognition modes of RNA tetraloops and tetraloop-like motifs by RNA-binding proteins.

Authors:  Roopa Thapar; Andria P Denmon; Edward P Nikonowicz
Journal:  Wiley Interdiscip Rev RNA       Date:  2013-10-03       Impact factor: 9.957

7.  A molecular switch underlies a human telomerase disease.

Authors:  Luis R Comolli; Ivan Smirnov; Lifeng Xu; Elizabeth H Blackburn; Thomas L James
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-13       Impact factor: 11.205

8.  Free energy profile of RNA hairpins: a molecular dynamics simulation study.

Authors:  Nan-Jie Deng; Piotr Cieplak
Journal:  Biophys J       Date:  2010-02-17       Impact factor: 4.033

9.  A high affinity binding site for the HIV-1 nucleocapsid protein.

Authors:  J A Berglund; B Charpentier; M Rosbash
Journal:  Nucleic Acids Res       Date:  1997-03-01       Impact factor: 16.971

10.  mRNA secondary structures fold sequentially but exchange rapidly in vivo.

Authors:  Elisabeth M Mahen; Peter Y Watson; Joseph W Cottrell; Martha J Fedor
Journal:  PLoS Biol       Date:  2010-02-09       Impact factor: 8.029

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