Literature DB >> 30912490

The kink-turn in the structural biology of RNA.

Lin Huang1, David M J Lilley1.   

Abstract

The kink-turn (k-turn) is a widespread structural motif found in functional RNA species. It typically comprises a three-nucleotide bulge followed by tandem trans sugar edge-Hoogsteen G:A base pairs. It introduces a sharp kink into the axis of duplex RNA, juxtaposing the minor grooves. Cross-strand H-bonds form at the interface, accepted by the conserved adenine nucleobases of the G:A basepairs. Alternative acceptors for one of these divides the k-turns into two conformational classes N3 and N1. The base pair that follows the G:A pairs (3b:3n) determines which conformation is adopted by a given k-turn. k-turns often mediate tertiary contacts in folded RNA species and frequently bind proteins. Common k-turn binding proteins include members of the L7Ae family, such as the human 15·5k protein. A recognition helix within these proteins binds in the widened major groove on the outside of the k-turn, that makes specific H-bonds with the conserved guanine nucleobases of the G:A pairs. L7Ae binds with extremely high affinity, and single-molecule data are consistent with folding by conformational selection. The standard, simple k-turn can be elaborated in a variety of ways, that include the complex k-turns and the k-junctions. In free solution in the absence of added metal ions or protein k-turns do not adopt the tightly-kinked conformation. They undergo folding by the binding of proteins, by the formation of tertiary contacts, and some (but not all) will fold on the addition of metal ions. Whether or not folding occurs in the presence of metal ions depends on local sequence, including the 3b:3n position, and the -1b:-1n position (5' to the bulge). In most cases -1b:-1n = C:G, so that the 3b:3n position is critical since it determines both folding properties and conformation. In general, the selection of these sequence matches a given k-turn to its biological requirements. The k-turn structure is now very well understood, to the point at which they can be used as a building block for the formation of RNA nano-objects, including triangles and squares.

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Year:  2018        PMID: 30912490     DOI: 10.1017/S0033583518000033

Source DB:  PubMed          Journal:  Q Rev Biophys        ISSN: 0033-5835            Impact factor:   5.318


  10 in total

1.  Improving the Performance of the Amber RNA Force Field by Tuning the Hydrogen-Bonding Interactions.

Authors:  Petra Kührová; Vojtěch Mlýnský; Marie Zgarbová; Miroslav Krepl; Giovanni Bussi; Robert B Best; Michal Otyepka; Jiří Šponer; Pavel Banáš
Journal:  J Chem Theory Comput       Date:  2019-04-02       Impact factor: 6.006

2.  Simulation Study of the Plasticity of k-Turn Motif in Different Environments.

Authors:  Haomiao Zhang; Haozhe Zhang; Changjun Chen
Journal:  Biophys J       Date:  2020-08-20       Impact factor: 4.033

3.  RNA kink-turns are highly anisotropic with respect to lateral displacement of the flanking stems.

Authors:  Eva Matoušková; Tomáš Dršata; Lucie Pfeifferová; Jiří Šponer; Kamila Réblová; Filip Lankaš
Journal:  Biophys J       Date:  2022-02-03       Impact factor: 4.033

4.  Structure and folding of four putative kink turns identified in structured RNA species in a test of structural prediction rules.

Authors:  Lin Huang; Xinli Liao; Mengxiao Li; Jia Wang; Xuemei Peng; Timothy J Wilson; David M J Lilley
Journal:  Nucleic Acids Res       Date:  2021-06-04       Impact factor: 16.971

5.  Effect of methylation of adenine N6 on kink turn structure depends on location.

Authors:  Saira Ashraf; Lin Huang; David M J Lilley
Journal:  RNA Biol       Date:  2019-06-24       Impact factor: 4.652

6.  Profiling of RNA ribose methylation in Arabidopsis thaliana.

Authors:  Songlin Wu; Yuqiu Wang; Jiayin Wang; Xilong Li; Jiayang Li; Keqiong Ye
Journal:  Nucleic Acids Res       Date:  2021-04-19       Impact factor: 16.971

7.  Elucidation of structure-function relationships in Methanocaldococcus jannaschii RNase P, a multi-subunit catalytic ribonucleoprotein.

Authors:  Hong-Duc Phan; Andrew S Norris; Chen Du; Kye Stachowski; Bela H Khairunisa; Vaishnavi Sidharthan; Biswarup Mukhopadhyay; Mark P Foster; Vicki H Wysocki; Venkat Gopalan
Journal:  Nucleic Acids Res       Date:  2022-08-12       Impact factor: 19.160

8.  Functional organization of box C/D RNA-guided RNA methyltransferase.

Authors:  Zuxiao Yang; Jiayin Wang; Lin Huang; David M J Lilley; Keqiong Ye
Journal:  Nucleic Acids Res       Date:  2020-05-21       Impact factor: 16.971

Review 9.  Modulating Immune Response with Nucleic Acid Nanoparticles.

Authors:  Jake K Durbin; Daniel K Miller; Julia Niekamp; Emil F Khisamutdinov
Journal:  Molecules       Date:  2019-10-17       Impact factor: 4.411

10.  Eukaryotic Box C/D methylation machinery has two non-symmetric protein assembly sites.

Authors:  Simone Höfler; Peer Lukat; Wulf Blankenfeldt; Teresa Carlomagno
Journal:  Sci Rep       Date:  2021-09-02       Impact factor: 4.379

  10 in total

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