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Developmental mRNA m5C landscape and regulatory innovations of massive m5C modification of maternal mRNAs in animals

Author

Listed:
  • Jianheng Liu

    (Sun Yat-Sen University)

  • Tao Huang

    (Sun Yat-Sen University)

  • Wanying Chen

    (Sun Yat-Sen University)

  • Chenhui Ding

    (Sun Yat-Sen University)

  • Tianxuan Zhao

    (Sun Yat-Sen University)

  • Xueni Zhao

    (Sun Yat-Sen University)

  • Bing Cai

    (Sun Yat-Sen University)

  • Yusen Zhang

    (Sun Yat-Sen University)

  • Song Li

    (Sun Yat-Sen University)

  • Ling Zhang

    (Sun Yat-Sen University)

  • Maoguang Xue

    (Zhejiang University School of Medicine
    Zhejiang University School of Medicine)

  • Xiuju He

    (Sun Yat-Sen University)

  • Wanzhong Ge

    (Zhejiang University School of Medicine
    Zhejiang University School of Medicine
    Zhejiang University)

  • Canquan Zhou

    (Sun Yat-Sen University)

  • Yanwen Xu

    (Sun Yat-Sen University)

  • Rui Zhang

    (Sun Yat-Sen University)

Abstract

m5C is one of the longest-known RNA modifications, however, its developmental dynamics, functions, and evolution in mRNAs remain largely unknown. Here, we generate quantitative mRNA m5C maps at different stages of development in 6 vertebrate and invertebrate species and find convergent and unexpected massive methylation of maternal mRNAs mediated by NSUN2 and NSUN6. Using Drosophila as a model, we reveal that embryos lacking maternal mRNA m5C undergo cell cycle delays and fail to timely initiate maternal-to-zygotic transition, implying the functional importance of maternal mRNA m5C. From invertebrates to the lineage leading to humans, two waves of m5C regulatory innovations are observed: higher animals gain cis-directed NSUN2-mediated m5C sites at the 5' end of the mRNAs, accompanied by the emergence of more structured 5'UTR regions; humans gain thousands of trans-directed NSUN6-mediated m5C sites enriched in genes regulating the mitotic cell cycle. Collectively, our studies highlight the existence and regulatory innovations of a mechanism of early embryonic development and provide key resources for elucidating the role of mRNA m5C in biology and disease.

Suggested Citation

  • Jianheng Liu & Tao Huang & Wanying Chen & Chenhui Ding & Tianxuan Zhao & Xueni Zhao & Bing Cai & Yusen Zhang & Song Li & Ling Zhang & Maoguang Xue & Xiuju He & Wanzhong Ge & Canquan Zhou & Yanwen Xu &, 2022. "Developmental mRNA m5C landscape and regulatory innovations of massive m5C modification of maternal mRNAs in animals," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-30210-0
    DOI: 10.1038/s41467-022-30210-0
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    Cited by:

    1. Jianheng Liu & Tao Huang & Jing Yao & Tianxuan Zhao & Yusen Zhang & Rui Zhang, 2023. "Epitranscriptomic subtyping, visualization, and denoising by global motif visualization," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    2. You Wu & Wenna Shao & Mengxiao Yan & Yuqin Wang & Pengfei Xu & Guoqiang Huang & Xiaofei Li & Brian D. Gregory & Jun Yang & Hongxia Wang & Xiang Yu, 2024. "Transfer learning enables identification of multiple types of RNA modifications using nanopore direct RNA sequencing," Nature Communications, Nature, vol. 15(1), pages 1-19, December.
    3. Lior Fishman & Avani Modak & Gal Nechooshtan & Talya Razin & Florian Erhard & Aviv Regev & Jeffrey A. Farrell & Michal Rabani, 2024. "Cell-type-specific mRNA transcription and degradation kinetics in zebrafish embryogenesis from metabolically labeled single-cell RNA-seq," Nature Communications, Nature, vol. 15(1), pages 1-20, December.
    4. Jing Zhang & Huili Li & Lee A. Niswander, 2024. "m5C methylated lncRncr3–MeCP2 interaction restricts miR124a-initiated neurogenesis," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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