Generation of conditional Hoxc8 loss-of-function and Hoxc8→Hoxc9 replacement alleles in mice

Jessica Blackburn, Melissa Rich, Nima Ghitani, Jeh Ping Liu

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

The Hox family of transcription factors are expressed at different domains along the rostrocaudal (R-C) body axis during development. To examine the function of Hoxc8 and Hoxc9 in specific cell types and at different developmental times, we have generated and characterized loxP flanked (floxed) Hoxc8 and Hoxc8→Hoxc9 replacement alleles of mice, with either GFP or LacZ reporters. Although all four alleles of mice behave like wild-type controls in motor behavioral testing, slight differences in endogenous Hox gene expression were observed among these alleles depending on the type of reporters used and the presence of Hoxc9 cDNA in the targeting constructs. The efficiency of Cre-mediated recombination was evaluated by crossing these mice with the Nestin-cre and Isl1-cre mice, and the loss of Hoxc8 expression with or without Hoxc9 mis-expression was confirmed in embryonic spinal cord. In addition, an upregulation of reporter gene expression was observed after Cre-mediated recombination. These mice will be useful tools to analyze Hox gene function in a cell type-specific manner.

Original languageEnglish
Pages (from-to)680-687
Number of pages8
JournalGenesis
Volume47
Issue number10
DOIs
StatePublished - 2009

Funding

FundersFunder number
National Institute of Neurological Disorders and StrokeR01NS045933

    Keywords

    • Cre-loxP
    • Gene targeting
    • Hoxc8
    • Hoxc9
    • Mouse

    ASJC Scopus subject areas

    • Genetics
    • Endocrinology
    • Cell Biology

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