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Full-term development of mice from enucleated oocytes injected with cumulus cell nuclei

Author

Listed:
  • T. Wakayama

    (John A. Burns School of Medicine, University of Hawaii
    Faculty of Agriculture, University of Tokyo)

  • A. C. F. Perry

    (John A. Burns School of Medicine, University of Hawaii
    Babraham Institute)

  • M. Zuccotti

    (John A. Burns School of Medicine, University of Hawaii
    Laboratorio Biologia dello Sviluppo, University of Pavia)

  • K. R. Johnson

    (Jackson Laboratory)

  • R. Yanagimachi

    (John A. Burns School of Medicine, University of Hawaii)

Abstract

Until recently, fertilization was the only way to produce viable mammalian offspring, a process implicitly involving male and female gametes. However, techniques involving fusion of embryonic or fetal somatic cells with enucleated oocytes have become steadily more successful in generating cloned young1,2,3. Dolly the sheep4 was produced by electrofusion of sheep mammary-derived cells with enucleated sheep oocytes. Here we investigate the factors governing embryonic development by introducing nuclei from somatic cells (Sertoli, neuronal and cumulus cells) taken from adult mice into enucleated mouse oocytes. We found that some enucleated oocytes receiving Sertoli or neuronal nuclei developed in vitro and implanted following transfer, but none developed beyond 8.5 days post coitum; however, a high percentage of enucleated oocytes receiving cumulus nuclei developed in vitro. Once transferred, many of these embryos implanted and, although most were subsequently resorbed, a significant proportion (2 to 2.8%) developed to term. These experiments show that for mammals, nuclei from terminally differentiated, adult somatic cells of known phenotype introduced into enucleated oocytes are capable of supporting full development.

Suggested Citation

  • T. Wakayama & A. C. F. Perry & M. Zuccotti & K. R. Johnson & R. Yanagimachi, 1998. "Full-term development of mice from enucleated oocytes injected with cumulus cell nuclei," Nature, Nature, vol. 394(6691), pages 369-374, July.
  • Handle: RePEc:nat:nature:v:394:y:1998:i:6691:d:10.1038_28615
    DOI: 10.1038/28615
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    Cited by:

    1. Sayaka Wakayama & Daiyu Ito & Erika Hayashi & Takashi Ishiuchi & Teruhiko Wakayama, 2022. "Healthy cloned offspring derived from freeze-dried somatic cells," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    2. M. Samiec & M. Skrzyszowska, 2005. "Microsurgical nuclear transfer by intraooplasmic karyoplast injection as an alternative embryo reconstruction method in somatic cloning of pigs and other mammal species; application value of the metho," Czech Journal of Animal Science, Czech Academy of Agricultural Sciences, vol. 50(6), pages 235-242.
    3. Ruimin Xu & Qianshu Zhu & Yuyan Zhao & Mo Chen & Lingyue Yang & Shijun Shen & Guang Yang & Zhifei Shi & Xiaolei Zhang & Qi Shi & Xiaochen Kou & Yanhong Zhao & Hong Wang & Cizhong Jiang & Chong Li & Sh, 2023. "Unreprogrammed H3K9me3 prevents minor zygotic genome activation and lineage commitment in SCNT embryos," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    4. Onaizah Onaizah & Liangcheng Xu & Kevin Middleton & Lidan You & Eric Diller, 2020. "Local stimulation of osteocytes using a magnetically actuated oscillating beam," PLOS ONE, Public Library of Science, vol. 15(6), pages 1-15, June.
    5. Zhaodi Liao & Jixiang Zhang & Shiyu Sun & Yuzhuo Li & Yuting Xu & Chunyang Li & Jing Cao & Yanhong Nie & Zhuoyue Niu & Jingwen Liu & Falong Lu & Zhen Liu & Qiang Sun, 2024. "Reprogramming mechanism dissection and trophoblast replacement application in monkey somatic cell nuclear transfer," Nature Communications, Nature, vol. 15(1), pages 1-18, December.

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