The targeting vector has been generated using C57BL/6J DNA and transfected into C57BL/6NTac ES cell line.
Mmp27 exon 1 contains the translation initiation codon.
Exon 2 has been flanked by loxP sites.
The constitutive KO allele has been generated after Cre-mediated recombination by crossing chimeras to a Cre-Deleter on a C57BL/6 background.
The constitutive KO line has been subsequently backcrossed to C57BL/6NTac animals for at least 2 generations and the Cre-transgene was removed by segregation.
Deletion of exon 2 should result in loss of function of the Mmp27 gene by deleting the peptidase and generating a frameshift (premature stop codon in exon 3).
The remaining recombination sites are located in intron regions of the genome.
Datamining and Design performed in 2006.
Gene Family: Peptidase
Genetic Background: C57BL/6
Gene Symbol: Mmp27
Gene Accession Number: NM_001030289
Allele Type: KO
Source: Institut Clinique de la Souris (ICS), Illkirch, France
Availability: Cryopreserved at Taconic
Official Gene Name: matrix metallopeptidase 27