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<p>As one of the most prevalent messenger RNA modifications in eukaryotes, <i>N</i><sup>6</sup>-methyladenosine (m<sup>6</sup>A) regulates various physiological and pathological processes. The RNA m<sup>6</sup>A sequencing techniques have significantly advanced the understanding of m<sup>6</sup>A biology, however, there is a lack of tools to <i>in situ</i> spatially characterize RNA m<sup>6</sup>A and its interacting components inside cells. Spatial information could significantly promote our understanding of the m<sup>6</sup>A dynamics and functions in complex biological contexts. While traditional m<sup>6</sup>A antibody immunostaining method images global cellular m<sup>6</sup>A sites, we here develop a non-antibody-based fluorescent imaging tool to <i>in situ</i> visualize single m<sup>6</sup>A site of specific cellular RNA, named m<sup>6</sup>A REading and Fluorescent Imaging <i>In situ</i> (m<sup>6</sup>A-REFII), which contains m<sup>6</sup>A reader module, hybridization probe module for targeting specific m<sup>6</sup>A-locating RNA sequence, and fluorescent signaling module. We successfully leveraged m<sup>6</sup>A-REFII to visualize m<sup>6</sup>A-modified RNAs at distinct subcellular localizations as well as to reveal the dynamic changes of targeted m<sup>6</sup>A sites in response to CRISPR-mediated m<sup>6</sup>A reduction and heat shock stimuli. Furthermore, we demonstrated the compatibility of m<sup>6</sup>A-REFII with protein immunofluorescence staining and validated the finding that the scaffold attachment factor B protein binds m<sup>6</sup>A-modified long interspersed element-1 RNA. Collectively, m<sup>6</sup>A-REFII is a new tool empowering visualization of single m<sup>6</sup>A modification on specific RNAs at the single-cell level.</p>

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m6A-REFII: an antibody-independent tool for in situ visualizing cellular specific RNA m6A compatible with protein immunofluorescence staining

  • 期刊论文

  • 发表日期：

    2025年6月11日

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  • Yujie Mi,
  • Chenyang Huang,
  • Donghong Liu,
  • Tengwei Li,
  • Xiner Ying,
  • Jie Cao,
  • Jianzhao Liu

摘要

As one of the most prevalent messenger RNA modifications in eukaryotes, N6-methyladenosine (m6A) regulates various physiological and pathological processes. The RNA m6A sequencing techniques have significantly advanced the understanding of m6A biology, however, there is a lack of tools to in situ spatially characterize RNA m6A and its interacting components inside cells. Spatial information could significantly promote our understanding of the m6A dynamics and functions in complex biological contexts. While traditional m6A antibody immunostaining method images global cellular m6A sites, we here develop a non-antibody-based fluorescent imaging tool to in situ visualize single m6A site of specific cellular RNA, named m6A REading and Fluorescent Imaging In situ (m6A-REFII), which contains m6A reader module, hybridization probe module for targeting specific m6A-locating RNA sequence, and fluorescent signaling module. We successfully leveraged m6A-REFII to visualize m6A-modified RNAs at distinct subcellular localizations as well as to reveal the dynamic changes of targeted m6A sites in response to CRISPR-mediated m6A reduction and heat shock stimuli. Furthermore, we demonstrated the compatibility of m6A-REFII with protein immunofluorescence staining and validated the finding that the scaffold attachment factor B protein binds m6A-modified long interspersed element-1 RNA. Collectively, m6A-REFII is a new tool empowering visualization of single m6A modification on specific RNAs at the single-cell level.