Brain transcriptional stability upon prion protein-encoding gene invalidation in zygotic or adult mouse
2010

Brain Stability After Prion Protein Gene Invalidation in Mice

Sample size: 10 publication 10 minutes Evidence: moderate

Author Information

Author(s): Chadi Sead, Rachel Young, Sandrine Le Guillou, Gaëlle Tilly, Frédérique Bitton, Marie-Laure Martin-Magniette, Ludivine Soubigou-Taconnat, Sandrine Balzergue, Marthe Vilotte, Coralie Peyre, Bruno Passet, Vincent Béringue, Jean-Pierre Renou, Fabienne Le Provost, Hubert Laude, Jean-Luc Vilotte

Primary Institution: INRA, UMR1313, Génétique Animale et Biologie Intégrative, Jouy-en-Josas, France

Hypothesis

What is the physiological function of the prion protein in the brain?

Conclusion

The study suggests that the physiological function of the prion protein is redundant in adult mice or only important for a small subset of brain cells.

Supporting Evidence

  • Only subtle transcriptomic differences were observed in the brains of Prnp knockout mice.
  • Neuronal Prnp disruption induced a response to oxidative stress and remodeling of the nervous system.
  • The study suggests that PrP may have a more detrimental role during embryogenesis.

Takeaway

The prion protein in the brain doesn't seem to change much when it's removed in adult mice, which means it might not be very important for brain function.

Methodology

Comparative transcriptomic analysis using microarray and QPCR on brain samples from wild-type and Prnp knockout mice.

Potential Biases

Potential bias due to the genetic background of the mice used in the study.

Limitations

The study may not capture all cellular responses due to the mixed cell population in adult brain tissues.

Participant Demographics

Mice of FVB/N genetic background, including both wild-type and Prnp knockout.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1471-2164-11-448

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