18th International Mouse Genome Conference17-22 October 2004, Seattle, USA
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POSTER 43 - MOUSE HAIRY EARS (EH) INVERSION MUTATION DISRUPTS NO GENE TRANSCRIPTS, BUT EXPRESSION OF HOXC GENES IN SKIN IS DISTURBED
Mentzer S 1, Sundberg J 2, Cacheiro N 1, Chao H 3, Carpenter D 1, Johnson D 1, Rinchik E 3, You Y 1
1 Oak Ridge National Laboratory, Oak Ridge, United States, 2 The Jackson Laboratory, Bar Harbor, United States, 3 University of Tennessee, Knoxville, United States
The mouse Hairy Ears (Eh) mutation is a paracentric inversion, In(15)Eh2Rl, in the distal half of Chr 15. Heterozygous Eh/+ mice have small and hairy ears, whereas Eh/Eh homozygotes in C3H/Rl background typically die before weaning. We mapped both the proximal and distal inversion breakpoints to BAC clones using fluorescent in situ hybridization (FISH) on metaphase Eh/+ cell spreads, cloned the distal breakpoint, and determined inversion breakpoint sequences. Consequently, genes surrounding the inversion breakpoints were identified. No protein-coding transcripts are disrupted by either inversion breakpoints. The proximal breakpoint occurs between Sntb1 (syntrophin 1, centromerically) and Has2 (hyaluronan synthase 2, telomerically), while the distal breakpoint takes place between the Hoxc4 (Homeobox C4, centromerically) and an uncharacterized transcript (GenBank accession numbers: BF606930 and AK019974, telomerically). Therefore the inversion spans ~47 Mb. Quantitative RNA analysis by TaqMan real-time PCR assay for the Hoxc genes indicated that expression of many members of Hoxc has been changed in skin during skin/hair morphogenesis and in adult mice. Hair fiber analysis using scanning electron microscopy revealed that ear-specific hair fibers grow longer in the ears of the Eh mutation. Histology analysis of ear-skin did not reveal any obvious abnormalities. Taken together, our results suggest that Hoxc genes play important roles in hair growth.
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