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Construction of a targeting vector by recombineering and generation of Cebpd conditional knockout mice for the study of cell-type specific functions of C/EBPdelta in vivo

Posted on:2014-03-09Degree:M.SType:Thesis
University:Hood CollegeCandidate:Sharan, ShikhaFull Text:PDF
GTID:2454390008450140Subject:Health Sciences
Abstract/Summary:PDF Full Text Request
The Cebpd gene encodes the transcription factor C/EBPdelta. A germ line deletion of the Cebpd gene in mice increased tumor multiplicity but reduced metastatic progression in a transgenic model of mammary tumorigenesis, indicating that C/EBPdelta can be both a tumor suppressor and tumor promoter. To address whether these phenotypes were caused by C/EBPdelta functions in mammary epithelial cells and/or cells of the tumor microenvironment, we needed a conditional knockout (cko) mouse model where the Cebpd gene can be deleted by cell-type specific expression of a Cre recombinase transgene. I have used homologous recombination technology to construct a cko targeting vector in which Cre recombination sites were placed on either side of the Cebpd coding region. This vector was used to generate mice carrying a Cebpd cko allele, and that can now be crossed into various mouse models to study cell-type specific deletions of Cebpd..
Keywords/Search Tags:Cell-type specific, C/ebpdelta, Targeting vector, Conditional knockout, Cebpd gene
PDF Full Text Request
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