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Prepublished online as a Blood First Edition Paper on July 17, 2003; DOI 10.1182/blood-2003-03-0966.

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Submitted March 28, 2003
Accepted June 23, 2003

The zebrafish spi1 promoter drives myeloid-specific expression in stable transgenic fish

Alister C Ward, Dora O McPhee, Melanie M Condron, Sony Varma, Stephen H Cody, Sara M Onnebo, Barry H Paw, Leonard I Zon, and Graham J Lieschke*

Cytokine Biology Laboratory, Ludwig Institute for Cancer Research, Parkville, VIC, Australia
Centre for Cellular and Molecular Biology, Deakin University, Burwood, VIC, Australia
Howard Hughes Medical Institute, Children's Hospital, Boston, MA, USA

* Corresponding author; email: Graham.Lieschke{at}ludwig.edu.au.

The spi1 (pu.1) gene has recently been identified as a useful marker of early myeloid cells in zebrafish. In order to enhance the versatility of this organism as a model for studying myeloid development, the promoter of this gene has been isolated and characterized. Transient transgenesis revealed that a 5.3 kb promoter fragment immediately upstream of the spi1 coding sequence was sufficient to drive expression of EGFP in injected embryos in a manner that largely recapitulated the native spi1 gene expression pattern. This fragment was successfully used to produce a germline transgenic line of zebrafish with EGFP-expressing myeloid cells. These TG(spi1:EGFP)pA301 transgenic zebrafish represent a valuable tool for further studies of myeloid development and its perturbation.


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