Literature DB >> 19741022

Three-way RNA junctions with remote tertiary contacts: a recurrent and highly versatile fold.

Marcos de la Peña1, David Dufour, José Gallego.   

Abstract

Three-way junction RNAs adopt a recurrent Y shape when two of the helices form a coaxial stack and the third helix establishes one or more tertiary contacts several base pairs away from the junction. In this review, the structure, distribution, and functional relevance of these motifs are examined. Structurally, the folds exhibit conserved junction topologies, and the distal tertiary interactions play a crucial role in determining the final shape of the structures. The junctions and remote tertiary contacts behave as flexible hinge motifs that respond to changes in the other region, providing these folds with switching mechanisms that have been shown to be functionally useful in a variety of contexts. In addition, the juxtaposition of RNA domains at the junction and at the distal tertiary complexes enables the RNA helices to adopt unusual conformations that are frequently used by proteins, RNA molecules, and antibiotics as platforms for specific binding. As a consequence of these properties, Y-shaped junctions are widely distributed in all kingdoms of life, having been observed in small naked RNAs such as riboswitches and ribozymes or embedded in complex ribonucleoprotein systems like ribosomal RNAs, RNase P, or the signal recognition particle. In all cases, the folds were found to play an essential role for the functioning or assembly of the RNA or ribonucleoprotein systems that contain them.

Mesh:

Substances:

Year:  2009        PMID: 19741022      PMCID: PMC2764472          DOI: 10.1261/rna.1889509

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  86 in total

1.  RNA tertiary interactions in the large ribosomal subunit: the A-minor motif.

Authors:  P Nissen; J A Ippolito; N Ban; P B Moore; T A Steitz
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-10       Impact factor: 11.205

2.  Crystal structure of the ribonucleoprotein core of the signal recognition particle.

Authors:  R T Batey; R P Rambo; L Lucast; B Rha; J A Doudna
Journal:  Science       Date:  2000-02-18       Impact factor: 47.728

3.  Is counterion delocalization responsible for collapse in RNA folding?

Authors:  V L Murthy; G D Rose
Journal:  Biochemistry       Date:  2000-11-28       Impact factor: 3.162

4.  Structure and assembly of the Alu domain of the mammalian signal recognition particle.

Authors:  O Weichenrieder; K Wild; K Strub; S Cusack
Journal:  Nature       Date:  2000-11-09       Impact factor: 49.962

5.  Role of SRP19 in assembly of the Archaeoglobus fulgidus signal recognition particle.

Authors:  J L Diener; C Wilson
Journal:  Biochemistry       Date:  2000-10-24       Impact factor: 3.162

6.  The complete atomic structure of the large ribosomal subunit at 2.4 A resolution.

Authors:  N Ban; P Nissen; J Hansen; P B Moore; T A Steitz
Journal:  Science       Date:  2000-08-11       Impact factor: 47.728

7.  Structure of the 30S ribosomal subunit.

Authors:  B T Wimberly; D E Brodersen; W M Clemons; R J Morgan-Warren; A P Carter; C Vonrhein; T Hartsch; V Ramakrishnan
Journal:  Nature       Date:  2000-09-21       Impact factor: 49.962

8.  A universal mode of helix packing in RNA.

Authors:  E A Doherty; R T Batey; B Masquida; J A Doudna
Journal:  Nat Struct Biol       Date:  2001-04

9.  The structural basis of ribosome activity in peptide bond synthesis.

Authors:  P Nissen; J Hansen; N Ban; P B Moore; T A Steitz
Journal:  Science       Date:  2000-08-11       Impact factor: 47.728

10.  Assembly of archaeal signal recognition particle from recombinant components.

Authors:  S H Bhuiyan; K Gowda; H Hotokezaka; C Zwieb
Journal:  Nucleic Acids Res       Date:  2000-03-15       Impact factor: 16.971

View more
  43 in total

Review 1.  The ubiquitous hammerhead ribozyme.

Authors:  Christian Hammann; Andrej Luptak; Jonathan Perreault; Marcos de la Peña
Journal:  RNA       Date:  2012-03-27       Impact factor: 4.942

2.  Ubiquitous presence of the hammerhead ribozyme motif along the tree of life.

Authors:  Marcos de la Peña; Inmaculada García-Robles
Journal:  RNA       Date:  2010-08-12       Impact factor: 4.942

3.  Structure of the three-way helical junction of the hepatitis C virus IRES element.

Authors:  Jonathan Ouellet; Sonya Melcher; Asif Iqbal; Yiliang Ding; David M J Lilley
Journal:  RNA       Date:  2010-06-25       Impact factor: 4.942

4.  Rapid construction of empirical RNA fitness landscapes.

Authors:  Jason N Pitt; Adrian R Ferré-D'Amaré
Journal:  Science       Date:  2010-10-15       Impact factor: 47.728

5.  Mapping L1 ligase ribozyme conformational switch.

Authors:  George M Giambaşu; Tai-Sung Lee; William G Scott; Darrin M York
Journal:  J Mol Biol       Date:  2012-07-03       Impact factor: 5.469

6.  Structure-function analysis from the outside in: long-range tertiary contacts in RNA exhibit distinct catalytic roles.

Authors:  Tara L Benz-Moy; Daniel Herschlag
Journal:  Biochemistry       Date:  2011-09-19       Impact factor: 3.162

7.  Investigation of the Melting Behavior of DNA Three-Way Junctions in the Closed and Open States.

Authors:  Carolyn E Carr; Luis A Marky
Journal:  Biophys J       Date:  2017-08-08       Impact factor: 4.033

8.  Increased Flexibility between Stems of Intramolecular Three-Way Junctions by the Insertion of Bulges.

Authors:  Carolyn E Carr; Luis A Marky
Journal:  Biophys J       Date:  2018-06-19       Impact factor: 4.033

9.  A general design strategy for protein-responsive riboswitches in mammalian cells.

Authors:  Simon Ausländer; Pascal Stücheli; Charlotte Rehm; David Ausländer; Jörg S Hartig; Martin Fussenegger
Journal:  Nat Methods       Date:  2014-10-05       Impact factor: 28.547

10.  iTRAQ quantitative analysis of multidrug resistance mechanisms in human gastric cancer cells.

Authors:  Huai-Dong Hu; Feng Ye; Da-Zhi Zhang; Peng Hu; Hong Ren; Sang-Lin Li
Journal:  J Biomed Biotechnol       Date:  2010-06-06
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.