4.4 Article

Rapid and efficient genetic manipulation of gyrencephalic carnivores using in utero electroporation

Journal

MOLECULAR BRAIN
Volume 5, Issue -, Pages -

Publisher

BIOMED CENTRAL LTD
DOI: 10.1186/1756-6606-5-24

Keywords

Ferrets; Cerebral cortex; in utero electroporation

Categories

Funding

  1. 21st Century COE Program Center for Integrated Brain Medical Sciences from the Ministry of Education, Culture, Sports, Science and Technology (MEXT)
  2. Global COE Program Comprehensive Center of Education and Research for Chemical Biology of the Diseases from MEXT, PRESTO from Japan Science and Technology Agency, Human Frontier Science Program
  3. Takeda Science Foundation
  4. Takeda Medical Research Foundation
  5. Astellas Foundation for Research on Metabolic Disorders
  6. Life Science Foundation of Japan
  7. Kurata Memorial Hitachi Science and Technology Foundation
  8. Mitsubishi Foundation
  9. Fukuda Foundation for Medical Technology
  10. Yamada Science Foundation
  11. Hokuto Foundation
  12. Daiichi-Sankyo Foundation of Life Sciences
  13. Research Foundation for Opto-Science and Technology
  14. Santen Pharmaceutical

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Background: Higher mammals such as primates and carnivores have highly developed unique brain structures such as the ocular dominance columns in the visual cortex, and the gyrus and outer subventricular zone of the cerebral cortex. However, our molecular understanding of the formation, function and diseases of these structures is still limited, mainly because genetic manipulations that can be applied to higher mammals are still poorly available. Results: Here we developed and validated a rapid and efficient technique that enables genetic manipulations in the brain of gyrencephalic carnivores using in utero electroporation. Transgene-expressing ferret babies were obtained within a few weeks after electroporation. GFP expression was detectable in the embryo and was observed at least 2 months after birth. Our technique was useful for expressing transgenes in both superficial and deep cortical neurons, and for examining the dendritic morphologies and axonal trajectories of GFP-expressing neurons in ferrets. Furthermore, multiple genes were efficiently co-expressed in the same neurons. Conclusion: Our method promises to be a powerful tool for investigating the fundamental mechanisms underlying the development, function and pathophysiology of brain structures which are unique to higher mammals.

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