Normal corpus callosum in Emx1 mutant mice with C57BL/6 background

Citation
Hl. Guo et al., Normal corpus callosum in Emx1 mutant mice with C57BL/6 background, BIOC BIOP R, 276(2), 2000, pp. 649-653
Citations number
22
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
276
Issue
2
Year of publication
2000
Pages
649 - 653
Database
ISI
SICI code
0006-291X(20000924)276:2<649:NCCIEM>2.0.ZU;2-E
Abstract
The Emx1 gene is a mouse homologue of a Drosophila head gap gene, empty spi racles. Corpus callosum defects have been reported for mutant mice lacking the Emx1 gene, indicating a possible involvement of the Emx1 gene in the re gulation of axon guidance during development. However, it has recently come to light that genetic background could influence the outcome of the corpus callosum defects in mutant mice generated by ES cell technology. To invest igate whether the corpus callosum defects resulted directly from Emx1 gene inactivation, we backcrossed the Emx1 mutant mice into the C57BL/6 backgrou nd and found that the Emx1 homozygous mutant mice with the C57BL/6 backgrou nd showed a normal corpus callosum score even though the cross-sectional ar ea was 8% less than that of their wild-type littermates, indicating that ge netic background could change the pattern of corpus callosum defects in Emx 1 mutant mice. Furthermore, the indusium griseum and taenia tecta were alwa ys present and the cerebral cortical layers were well differentiated in Emx 1 mutant mice. These results suggest that inactivation of the Emx1 gene doe s not contribute directly to the defects of corpus callosum and other brain structures associated with Emx1 mutant mice derived from a 129/Sv backgrou nd. (C) 2000 Academic Press.