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Mice cloned from olfactory sensory neurons

Abstract

Cloning by nuclear transplantation has been successfully carried out in various mammals, including mice. Until now mice have not been cloned from post-mitotic cells such as neurons. Here, we have generated fertile mouse clones derived by transferring the nuclei of post-mitotic, olfactory sensory neurons into oocytes. These results indicate that the genome of a post-mitotic, terminally differentiated neuron can re-enter the cell cycle and be reprogrammed to a state of totipotency after nuclear transfer. Moreover, the pattern of odorant receptor gene expression and the organization of odorant receptor genes in cloned mice was indistinguishable from wild-type animals, indicating that irreversible changes to the DNA of olfactory neurons do not accompany receptor gene choice.

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Figure 1: Genetically marking post-mitotic OSNs.
Figure 2: Mice derived from OSN nuclei.
Figure 3: Mice produced from OSNs expressing the P2 odorant receptor.

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References

  1. Rideout, W. M., Eggan, K. & Jaenisch, R. Nuclear cloning and epigenetic reprogramming of the genome. Science 293, 1093–1098 (2001)

    Article  CAS  Google Scholar 

  2. Hochedlinger, K. & Jaenisch, R. Nuclear transplantation: lessons from frogs and mice. Curr. Opin. Cell Biol. 14, 741–748 (2002)

    Article  CAS  Google Scholar 

  3. Gurdon, J. B. & Byrne, J. A. The first half-century of nuclear transplantation. Proc. Natl Acad. Sci. USA 100, 8048–8052 (2003)

    Article  ADS  CAS  Google Scholar 

  4. Osada, T., Kusakabe, H., Akutsu, H., Yagi, T. & Yanagimachi, R. Adult murine neurons: their chromatin and chromosome changes and failure to support embryonic development as revealed by nuclear transfer. Cytogenet. Genome Res. 97, 7–12 (2002)

    Article  CAS  Google Scholar 

  5. Yamazaki, Y. et al. Assessment of the developmental totipotency of neural cells in the cerebral cortex of mouse embryo by nuclear transfer. Proc. Natl Acad. Sci. USA 98, 14022–14026 (2001)

    Article  ADS  CAS  Google Scholar 

  6. Chien, Y. H., Gascoigne, N. R., Kavaler, J., Lee, N. E. & Davis, M. M. Somatic recombination in a murine T-cell receptor gene. Nature 309, 322–326 (1984)

    Article  ADS  CAS  Google Scholar 

  7. Hozumi, N. & Tonegawa, S. Evidence for somatic rearrangement of immunoglobulin genes coding for variable and constant regions. Proc. Natl Acad. Sci. USA 73, 3628–3632 (1976)

    Article  ADS  CAS  Google Scholar 

  8. Brack, C., Hirama, M., Lenhard-Schuller, R. & Tonegawa, S. A complete immunoglobulin gene is created by somatic recombination. Cell 15, 1–14 (1978)

    Article  CAS  Google Scholar 

  9. Gao, Y. et al. A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis. Cell 95, 891–902 (1998)

    Article  CAS  Google Scholar 

  10. Frank, K. M. et al. Late embryonic lethality and impaired V(D)J recombination in mice lacking DNA ligase IV. Nature 396, 173–177 (1998)

    Article  ADS  CAS  Google Scholar 

  11. Rehen, S. K. et al. Chromosomal variation in neurons of the developing and adult mammalian nervous system. Proc. Natl Acad. Sci. USA 98, 13361–13366 (2001)

    Article  ADS  CAS  Google Scholar 

  12. Kaushal, D. et al. Alteration of gene expression by chromosome loss in the postnatal mouse brain. J. Neurosci. 23, 5599–5606 (2003)

    Article  CAS  Google Scholar 

  13. Chun, J. & Schatz, D. G. Rearranging views on neurogenesis: neuronal death in the absence of DNA end-joining proteins. Neuron 22, 7–10 (1999)

    Article  CAS  Google Scholar 

  14. Chun, J. Selected comparison of immune and nervous system development. Adv. Immunol. 77, 297–322 (2001)

    Article  CAS  Google Scholar 

  15. Yagi, T. Diversity of the cadherin-related neuronal receptor/protocadherin family and possible DNA rearrangement in the brain. Genes Cells 8, 1–8 (2003)

    Article  CAS  Google Scholar 

  16. Zhang, X. & Firestein, S. The olfactory receptor gene superfamily of the mouse. Nature Neurosci. 5, 124–133 (2002)

    Article  CAS  Google Scholar 

  17. Ressler, K. J., Sullivan, S. L. & Buck, L. B. A zonal organization of odorant receptor gene expression in the olfactory epithelium. Cell 73, 597–609 (1993)

    Article  CAS  Google Scholar 

  18. Vassar, R., Ngai, J. & Axel, R. Spatial segregation of odorant receptor expression in the mammalian olfactory epithelium. Cell 74, 309–318 (1993)

    Article  CAS  Google Scholar 

  19. Buck, L. & Axel, R. A novel multigene family may encode odorant receptors: a molecular basis for odor recognition. Cell 65, 175–187 (1991)

    Article  CAS  Google Scholar 

  20. Kratz, E., Dugas, J. C. & Ngai, J. Odorant receptor gene regulation: implications from genomic organization. Trends Genet. 18, 29–34 (2002)

    Article  CAS  Google Scholar 

  21. Goldstein, B. J. & Schwob, J. E. Analysis of the globose basal cell compartment in rat olfactory epithelium using GBC-1, a new monoclonal antibody against globose basal cells. J. Neurosci. 16, 4005–4016 (1996)

    Article  CAS  Google Scholar 

  22. Holbrook, E. H., Szumowski, K. E. & Schwob, J. E. An immunochemical, ultrastructural, and developmental characterization of the horizontal basal cells of rat olfactory epithelium. J. Comp. Neurol. 363, 129–146 (1995)

    Article  CAS  Google Scholar 

  23. Ohta, Y. & Ichimura, K. Proliferation markers, proliferating cell nuclear antigen, Ki67, 5-bromo-2′-deoxyuridine, and cyclin D1 in mouse olfactory epithelium. Ann. Otol. Rhinol. Laryngol. 109, 1046–1048 (2000)

    Article  CAS  Google Scholar 

  24. Gerdes, J. et al. Cell cycle analysis of a cell proliferation-associated human nuclear antigen defined by the monoclonal antibody Ki-67. J. Immunol. 133, 1710–1715 (1984)

    CAS  Google Scholar 

  25. Wakayama, T., Perry, A. C., Zuccotti, M., Johnson, K. R. & Yanagimachi, R. Full-term development of mice from enucleated oocytes injected with cumulus cell nuclei. Nature 394, 369–374 (1998)

    Article  ADS  CAS  Google Scholar 

  26. Wakayama, T., Rodriguez, I., Perry, A. C., Yanagimachi, R. & Mombaerts, P. Mice cloned from embryonic stem cells. Proc. Natl Acad. Sci. USA 96, 14984–14989 (1999)

    Article  ADS  CAS  Google Scholar 

  27. Rideout, W. M. et al. Generation of mice from wild-type and targeted ES cells by nuclear cloning. Nature Genet. 24, 109–110 (2000)

    Article  CAS  Google Scholar 

  28. Hochedlinger, K. & Jaenisch, R. Monoclonal mice generated by nuclear transfer from mature B and T donor cells. Nature 415, 1035–1038 (2002)

    Article  ADS  CAS  Google Scholar 

  29. Eggan, K. et al. Hybrid vigor, fetal overgrowth, and viability of mice derived by nuclear cloning and tetraploid embryo complementation. Proc. Natl Acad. Sci. USA 98, 6209–6214 (2001)

    Article  ADS  CAS  Google Scholar 

  30. Nagy, A. et al. Embryonic stem cells alone are able to support fetal development in the mouse. Development 110, 815–821 (1990)

    CAS  PubMed  Google Scholar 

  31. Wang, F., Nemes, A., Mendelsohn, M. & Axel, R. Odorant receptors govern the formation of a precise topographic map. Cell 93, 47–60 (1998)

    Article  CAS  Google Scholar 

  32. Gogos, J. A., Osborne, J., Nemes, A., Mendelsohn, M. & Axel, R. Genetic ablation and restoration of the olfactory topographic map. Cell 103, 609–620 (2000)

    Article  CAS  Google Scholar 

  33. Srinivas, S. et al. Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus. BMC Dev. Biol. 1, 4 (2001)

    Article  CAS  Google Scholar 

  34. Rossant, J. A monoclonal mouse? Nature 415, 967–969 (2002)

    Article  ADS  CAS  Google Scholar 

  35. Ohnuma, S. & Harris, W. A. Neurogenesis and the cell cycle. Neuron 40, 199–208 (2003)

    Article  CAS  Google Scholar 

  36. Edelman, G. M. Neural Darwinism (Basic Books, New York, NY, 1987)

    Google Scholar 

  37. Ishii, T. et al. Monoallelic expression of the odourant receptor gene and axonal projection of olfactory sensory neurones. Genes Cells 6, 71–78 (2001)

    Article  CAS  Google Scholar 

  38. Serizawa, S. et al. Negative feedback regulation ensures the one receptor-one olfactory neuron rule in mouse. Science 302, 2088–2094 (2003)

    Article  ADS  CAS  Google Scholar 

  39. Serizawa, S. et al. Mutually exclusive expression of odorant receptor transgenes. Nature Neurosci. 3, 687–693 (2000)

    Article  CAS  Google Scholar 

  40. Ebrahimi, F. A., Edmondson, J., Rothstein, R. & Chess, A. YAC transgene-mediated olfactory receptor gene choice. Dev. Dyn. 217, 225–231 (2000)

    Article  CAS  Google Scholar 

  41. Qasba, P. & Reed, R. R. Tissue and zonal-specific expression of an olfactory receptor transgene. J. Neurosci. 18, 227–236 (1998)

    Article  CAS  Google Scholar 

  42. Vassalli, A., Rothman, A., Feinstein, P., Zapotocky, M. & Mombaerts, P. Minigenes impart odorant receptor-specific axon guidance in the olfactory bulb. Neuron 35, 681–696 (2002)

    Article  CAS  Google Scholar 

  43. Sambrook, J., Fritsch, E. F. & Maniatis, T. Molecular Cloning: a Laboratory Manual 2nd edn (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1989)

    Google Scholar 

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Acknowledgements

We thank L. Moring, A. Nemes, M. Mendelsohn, J. Loring, J. Dausman, A. Meissner and K. Hochedlinger for assistance during the course of these experiments; T. Cutforth, J. de Nooij, T. Jessell and J. Johnson for sharing reagents necessary for our experiments; and members of the Jaenisch, Axel and Chess laboratories for discussion and assistance during the course of these experiments, especially F. A. Ebrahimi, M. Rios, W. M. R. Rideout, L. Jackson-Grusby and B. Shykind. This research was sponsored by NIH grants to R.J. and R.A. K.B. is an Associate and R.A. is an Investigator of the Howard Hughes Medical Institute. K.E. is a Junior Fellow in the Harvard Society of Fellows.

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Correspondence to Andrew Chess or Rudolf Jaenisch.

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Supplementary information

Supplementary Figure 1

Excision of the Rosa LoxP Stop LoxP cassette in ES cells cloned from P2-IRES-GFP expressing OSNS. (JPG 35 kb)

Supplementary Figure 2

ES cells cloned from P2 expressing OSNs bear only two copies of the P2 gene. (JPG 16 kb)

Supplementary Figure 3

Genomic organization of the P2-IRES-GFP locus in cloned mice. (JPG 61 kb)

Supplementary Figure Legends (DOC 20 kb)

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Eggan, K., Baldwin, K., Tackett, M. et al. Mice cloned from olfactory sensory neurons. Nature 428, 44–49 (2004). https://doi.org/10.1038/nature02375

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