4.8 Article

Double-stranded RNA bending by AU-tract sequences

期刊

NUCLEIC ACIDS RESEARCH
卷 48, 期 22, 页码 12917-12928

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkaa1128

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资金

  1. Spanish MINECO (AEI/FEDER, UE) [MAT2017-83273-R, BFU2017-83794-P]
  2. Comunidad de Madrid [S2018/NMT-4443, Y2018/BIO4747]
  3. Spanish Ministry of Science and Innovation, through the 'Maria de Maeztu' Programme for Units of Excellence in RD [CEX2018-000805-M]
  4. European Research Council (ERC) under the European Union Horizon 2020 research and innovation [681299]
  5. Marie Sklodowska-Curie Fellowship within the Horizons 2020 framework [DLV-795286]
  6. Swiss National Science Foundation [31003A_179256/1, CRSK-2 190731/1]
  7. International PhD Program of 'La Caixa-Severo Ochoa'
  8. Spanish Ministry of Competitiveness and Industry of a FPI fellowship [BES-2015-071244, PRE2018-083464]
  9. European Research Council (ERC) [681299]
  10. Swiss National Science Foundation (SNF) [CRSK-2_190731] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

Sequence-dependent structural deformations of the DNA double helix (dsDNA) have been extensively studied, where adenine tracts (A-tracts) provide a striking example for global bending in the molecule. However, in contrast to dsDNA, sequence-dependent structural features of dsRNA have received little attention. In this work, we demonstrate that the nucleotide sequence can induce a bend in a canonical Watson-Crick base-paired dsRNA helix. Using allatom molecular dynamics simulations, we identified a sequence motif consisting of alternating adenines and uracils, or AU-tracts, that strongly bend the RNA double-helix. This finding was experimentally validated using atomic force microscopy imaging of dsRNA molecules designed to display macroscopic curvature via repetitions of phased AU-tract motifs. At the atomic level, this novel phenomenon originates from a localized compression of the dsRNA major groove and a large propeller twist at the position of the AU-tract. Moreover, the magnitude of the bending can be modulated by changing the length of the AU-tract. Altogether, our results demonstrate the possibility of modifying the dsRNA curvature by means of its nucleotide sequence, which may be exploited in the emerging field of RNA nanotechnology and might also constitute a natural mechanism for proteins to achieve recognition of specific dsRNA sequences.

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