Stabilization of VEGF i-motif structure by CpG methylation

The intercalated motif (i-motif) is a non-canonical nucleic acid structure formed by intercalated hemi-protonated cytosine base pairs (C–C+) under acidic conditions. The i-motif structure formation is involved in biological processes such as transcription regulation. Therefore, the identification of...

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Veröffentlicht in:Biochemical and biophysical research communications 2022-02, Vol.594, p.88-92
Hauptverfasser: Kimura, Kosuke, Oshikawa, Daiki, Ikebukuro, Kazunori, Yoshida, Wataru
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Oshikawa, Daiki
Ikebukuro, Kazunori
Yoshida, Wataru
description The intercalated motif (i-motif) is a non-canonical nucleic acid structure formed by intercalated hemi-protonated cytosine base pairs (C–C+) under acidic conditions. The i-motif structure formation is involved in biological processes such as transcription regulation. Therefore, the identification of factors controlling i-motif formation is important in elucidating the cellular functions it controls. We previously reported that the VEGF G-quadruplex structure is stabilized by CpG methylation. In this study, the effect of CpG methylation on the stability of the VEGF i-motif structure was investigated. The VEGF i-motif-forming oligonucleotide contains four cytosines on CpG sites, and three of the four cytosines (C4, C15, and C20) are involved in C–C+ formation in the i-motif structure. Circular dichroism (CD) spectra analysis demonstrated that full CpG methylation increased the pH of mid transition (pHT) of the i-motif structure by 0.1, and the melting temperature (Tm) by 5.1 °C in 25 mM sodium cacodylate buffer at pH 5.0. Moreover, single methylation at C4, C15, and C20 increased Tm by 0.5, 1.7, and 2.0 °C in the buffer, respectively. These results demonstrated that CpG methylation stabilized the VEGF i-motif structure. [Display omitted] •Full CpG methylation increased the pH of mid transition of the VEGF i-motif by 0.1.•Full CpG methylation increased the melting temperature at pH 5.0 by 5.1 °C.•Methylation at cytosines involved in C–C+ formation stabilized the i-motif.
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The i-motif structure formation is involved in biological processes such as transcription regulation. Therefore, the identification of factors controlling i-motif formation is important in elucidating the cellular functions it controls. We previously reported that the VEGF G-quadruplex structure is stabilized by CpG methylation. In this study, the effect of CpG methylation on the stability of the VEGF i-motif structure was investigated. The VEGF i-motif-forming oligonucleotide contains four cytosines on CpG sites, and three of the four cytosines (C4, C15, and C20) are involved in C–C+ formation in the i-motif structure. Circular dichroism (CD) spectra analysis demonstrated that full CpG methylation increased the pH of mid transition (pHT) of the i-motif structure by 0.1, and the melting temperature (Tm) by 5.1 °C in 25 mM sodium cacodylate buffer at pH 5.0. Moreover, single methylation at C4, C15, and C20 increased Tm by 0.5, 1.7, and 2.0 °C in the buffer, respectively. 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These results demonstrated that CpG methylation stabilized the VEGF i-motif structure. [Display omitted] •Full CpG methylation increased the pH of mid transition of the VEGF i-motif by 0.1.•Full CpG methylation increased the melting temperature at pH 5.0 by 5.1 °C.•Methylation at cytosines involved in C–C+ formation stabilized the i-motif.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>35078112</pmid><doi>10.1016/j.bbrc.2022.01.054</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0001-9828-0896</orcidid></addata></record>
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subjects Amino Acid Motifs
Buffers
Circular Dichroism
CpG Islands
CpG methylation
Cytosine - chemistry
DNA Methylation
G-Quadruplexes
Humans
Hydrogen-Ion Concentration
i-motif
Intercalating Agents
Nucleic Acid Conformation
Oligonucleotides - chemistry
Protein Structure, Secondary
Temperature
Thermal stability
Vascular Endothelial Growth Factor A - chemistry
Vascular Endothelial Growth Factor A - metabolism
VEGF
title Stabilization of VEGF i-motif structure by CpG methylation
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