Author
Listed:
- Kevin Eggan
(Massachusetts Institute of Technology
Harvard University)
- Kristin Baldwin
(Howard Hughes Medical Institute, College of Physicians and Surgeons, Columbia University)
- Michael Tackett
(Massachusetts Institute of Technology)
- Joseph Osborne
(Howard Hughes Medical Institute, College of Physicians and Surgeons, Columbia University
College of Physicians and Surgeons, Columbia University)
- Joseph Gogos
(Howard Hughes Medical Institute, College of Physicians and Surgeons, Columbia University)
- Andrew Chess
(Massachusetts Institute of Technology)
- Richard Axel
(Howard Hughes Medical Institute, College of Physicians and Surgeons, Columbia University)
- Rudolf Jaenisch
(Massachusetts Institute of Technology)
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.
Suggested Citation
Kevin Eggan & Kristin Baldwin & Michael Tackett & Joseph Osborne & Joseph Gogos & Andrew Chess & Richard Axel & Rudolf Jaenisch, 2004.
"Mice cloned from olfactory sensory neurons,"
Nature, Nature, vol. 428(6978), pages 44-49, March.
Handle:
RePEc:nat:nature:v:428:y:2004:i:6978:d:10.1038_nature02375
DOI: 10.1038/nature02375
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