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Abstract Details

Expression Pattern of C9ORF72 Ortholog in Mice
Anterior Horn
S06 - (-)
004
Recently, a noncoding hexanucleotide repeat in C9ORF72 was identified as the cause of chromosome 9p-associated ALS and FTD. The C9ORF72 repeat expansion is a relatively common cause of ALS and FTD in Western population. Repeat expansion results in reduced expression of the major transcripts of C9ORF72, suggesting that haploinsufficiency may play a role in disease.
We used gene targeting to disrupt the expression of the C9ORF72 ortholog in mice using LacZ knock-in strategy.
We found high expression of C9ORF72 mouse ortholog in hippocampus, thalamus, brainstem and cerebral cortex. This gene is also transcribed in spinal cord, especially in the ventral horn. We didn't detect expression in skeletal muscle.
Our mice will be a useful tool to examine the expression pattern of C9ORF72, until antibodies have been identified that can reliably recognize C9ORF72. Also, we will describe preliminary results for phenotypes of C9ORF72 heterozygous and homozygous knockout animals.
Authors/Disclosures

PRESENTER
No disclosure on file
Joyce A. Cramer (Yale University School of Medicine) No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file