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Mol Cell Neurosci. 2009 Nov;42(3):161-71. doi: 10.1016/j.mcn.2009.06.010. Epub 2009 Jul 4.

Disorganized olfactory bulb lamination in mice deficient for transcription factor AP-2epsilon.

Author information

1
Department of Craniofacial Biology, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO 80045, USA.

Abstract

Within the olfactory bulb, neurons and their axonal connections are organized into distinct layers corresponding to different functionalities. Here we demonstrate that transcription factor AP-2epsilon is required for olfactory bulb development, specifically the establishment of appropriate neuronal lamination. During normal mouse embryogenesis, AP-2epsilon transcripts are one of the earliest markers of olfactory bulb formation, and expression eventually becomes refined to the projection neurons, the mitral and tufted cells. To assess the function of AP-2epsilon in olfaction, we generated a null allele (the "AK" allele) by inserting a Cre recombinase transgene into the endogenous AP-2epsilon genomic locus. AP-2epsilon-null mice exhibited defective olfactory bulb architecture. The mitral cell layer was disorganized, typified by misoriented and aberrantly positioned projection neurons, and the adjacent internal plexiform layer was absent. Despite the significant disruption of olfactory bulb organization, AP-2epsilon null mice were viable and could discriminate a variety of odors. AP-2epsilon-null mice thus provide compelling evidence for the robust nature of the mouse olfactory system, and serve as a model system to probe both the regulation of neuronal lamination and the functional circuitry of the olfactory bulb. We also show that Cre recombinase expression directed by the AP-2epsilon locus can specifically target floxed genes within the olfactory bulb, extending the utility of this AK allele.

PMID:
19580868
PMCID:
PMC2745980
DOI:
10.1016/j.mcn.2009.06.010
[Indexed for MEDLINE]
Free PMC Article

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