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N(6)-Methyladenosine Modification in a Long Noncoding RNA Hairpin Predisposes Its Conformation to Protein Binding.

Publication ,  Journal Article
Zhou, KI; Parisien, M; Dai, Q; Liu, N; Diatchenko, L; Sachleben, JR; Pan, T
Published in: J Mol Biol
February 27, 2016

N(6)-Methyladenosine (m(6)A) is a reversible and abundant internal modification of messenger RNA (mRNA) and long noncoding RNA (lncRNA) with roles in RNA processing, transport, and stability. Although m(6)A does not preclude Watson-Crick base pairing, the N(6)-methyl group alters the stability of RNA secondary structure. Since changes in RNA structure can affect diverse cellular processes, the influence of m(6)A on mRNA and lncRNA structure has the potential to be an important mechanism for m(6)A function in the cell. Indeed, an m(6)A site in the lncRNA metastasis associated lung adenocarcinoma transcript 1 (MALAT1) was recently shown to induce a local change in structure that increases the accessibility of a U5-tract for recognition and binding by heterogeneous nuclear ribonucleoprotein C (HNRNPC). This m(6)A-dependent regulation of protein binding through a change in RNA structure, termed "m(6)A-switch", affects transcriptome-wide mRNA abundance and alternative splicing. To further characterize this first example of an m(6)A-switch in a cellular RNA, we used nuclear magnetic resonance and Förster resonance energy transfer to demonstrate the effect of m(6)A on a 32-nucleotide RNA hairpin derived from the m(6)A-switch in MALAT1. The observed imino proton nuclear magnetic resonance resonances and Förster resonance energy transfer efficiencies suggest that m(6)A selectively destabilizes the portion of the hairpin stem where the U5-tract is located, increasing the solvent accessibility of the neighboring bases while maintaining the overall hairpin structure. The m(6)A-modified hairpin has a predisposed conformation that resembles the hairpin conformation in the RNA-HNRNPC complex more closely than the unmodified hairpin. The m(6)A-induced structural changes in the MALAT1 hairpin can serve as a model for a large family of m(6)A-switches that mediate the influence of m(6)A on cellular processes.

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Published In

J Mol Biol

DOI

EISSN

1089-8638

Publication Date

February 27, 2016

Volume

428

Issue

5 Pt A

Start / End Page

822 / 833

Location

Netherlands

Related Subject Headings

  • RNA, Messenger
  • RNA, Long Noncoding
  • Protein Binding
  • Nucleic Acid Conformation
  • Models, Molecular
  • Humans
  • Biochemistry & Molecular Biology
  • Alternative Splicing
  • Adenosine
  • 3107 Microbiology
 

Citation

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Zhou, K. I., Parisien, M., Dai, Q., Liu, N., Diatchenko, L., Sachleben, J. R., & Pan, T. (2016). N(6)-Methyladenosine Modification in a Long Noncoding RNA Hairpin Predisposes Its Conformation to Protein Binding. J Mol Biol, 428(5 Pt A), 822–833. https://doi.org/10.1016/j.jmb.2015.08.021
Zhou, Katherine I., Marc Parisien, Qing Dai, Nian Liu, Luda Diatchenko, Joseph R. Sachleben, and Tao Pan. “N(6)-Methyladenosine Modification in a Long Noncoding RNA Hairpin Predisposes Its Conformation to Protein Binding.J Mol Biol 428, no. 5 Pt A (February 27, 2016): 822–33. https://doi.org/10.1016/j.jmb.2015.08.021.
Zhou KI, Parisien M, Dai Q, Liu N, Diatchenko L, Sachleben JR, et al. N(6)-Methyladenosine Modification in a Long Noncoding RNA Hairpin Predisposes Its Conformation to Protein Binding. J Mol Biol. 2016 Feb 27;428(5 Pt A):822–33.
Zhou, Katherine I., et al. “N(6)-Methyladenosine Modification in a Long Noncoding RNA Hairpin Predisposes Its Conformation to Protein Binding.J Mol Biol, vol. 428, no. 5 Pt A, Feb. 2016, pp. 822–33. Pubmed, doi:10.1016/j.jmb.2015.08.021.
Zhou KI, Parisien M, Dai Q, Liu N, Diatchenko L, Sachleben JR, Pan T. N(6)-Methyladenosine Modification in a Long Noncoding RNA Hairpin Predisposes Its Conformation to Protein Binding. J Mol Biol. 2016 Feb 27;428(5 Pt A):822–833.
Journal cover image

Published In

J Mol Biol

DOI

EISSN

1089-8638

Publication Date

February 27, 2016

Volume

428

Issue

5 Pt A

Start / End Page

822 / 833

Location

Netherlands

Related Subject Headings

  • RNA, Messenger
  • RNA, Long Noncoding
  • Protein Binding
  • Nucleic Acid Conformation
  • Models, Molecular
  • Humans
  • Biochemistry & Molecular Biology
  • Alternative Splicing
  • Adenosine
  • 3107 Microbiology