Literature DB >> 10906144

Analysis of the functional role of a G.A sheared base pair by in vitro genetics.

B Sargueil1, J McKenna, J M Burke.   

Abstract

A classical genetic strategy has been combined with an in vitro selection method to search for functional interactions between the two domains of the hairpin ribozyme. G(21) is located within internal loop B; it is proposed to form a sheared base pair with A(43) across loop B and to bind a Mg(2+) ion. Both nucleotides are important for ribozyme function, and G.A sheared base pairs are a very widespread motif in structured RNA. We took advantage of its presence in the hairpin ribozyme to study its functional role. Pseudorevertants, in which the loss of G(21) was compensated by mutations at other positions, were isolated by in vitro selection. The vast majority of G(21) revertants contained substitutions within domain A, pointing to functional communication between specific sites within the two domains of the hairpin ribozyme. The possibility of a direct or redundant contacts is supported by electrophoretic mobility shift studies showing that a complex formed between domain B of the ribozyme and the substrate was disrupted and restored by base substitutions that have analogous effects on catalytic activity. The functional significance of this complex, the role of the nucleotides involved, and the basis for magnesium ion requirement is discussed.

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Year:  2000        PMID: 10906144     DOI: 10.1074/jbc.M005591200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  5 in total

Review 1.  Recent advances in the elucidation of the mechanisms of action of ribozymes.

Authors:  Y Takagi; M Warashina; W J Stec; K Yoshinari; K Taira
Journal:  Nucleic Acids Res       Date:  2001-05-01       Impact factor: 16.971

2.  Structural features of the Seneca Valley virus internal ribosome entry site (IRES) element: a picornavirus with a pestivirus-like IRES.

Authors:  Margaret M Willcocks; Nicolas Locker; Zarmwa Gomwalk; Elizabeth Royall; Mehran Bakhshesh; Graham J Belsham; Neeraja Idamakanti; Kevin D Burroughs; P Seshidhar Reddy; Paul L Hallenbeck; Lisa O Roberts
Journal:  J Virol       Date:  2011-02-16       Impact factor: 5.103

3.  A conserved structure within the HIV gag open reading frame that controls translation initiation directly recruits the 40S subunit and eIF3.

Authors:  Nicolas Locker; Nathalie Chamond; Bruno Sargueil
Journal:  Nucleic Acids Res       Date:  2010-11-11       Impact factor: 16.971

4.  A new type of IRES within gag coding region recruits three initiation complexes on HIV-2 genomic RNA.

Authors:  Laure Weill; Laurie James; Nathalie Ulryck; Nathalie Chamond; Cecile H Herbreteau; Theophile Ohlmann; Bruno Sargueil
Journal:  Nucleic Acids Res       Date:  2009-12-06       Impact factor: 16.971

5.  Functional analysis of Kaposi's sarcoma-associated herpesvirus vFLIP expression reveals a new mode of IRES-mediated translation.

Authors:  Zulkefley Othman; Mariam K Sulaiman; Margaret M Willcocks; Nathalie Ulryck; David J Blackbourn; Bruno Sargueil; Lisa O Roberts; Nicolas Locker
Journal:  RNA       Date:  2014-09-22       Impact factor: 4.942

  5 in total

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