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Richard Dorsky

Associate Professor of Neurobiology and Anatomy

B.A. University of California, Berkeley

Ph.D. University of California, San Diego

Research

References

richard.dorsky@neuro.utah.edu

Rich Dorsky's PubMed Literature Search

Research

During development of the central nervous system (CNS), cells are influenced by their environment to adopt specific fates.   These environmental signals are crucial for the correct patterning of cell types and their subsequent functional connections.   My laboratory is studying the role of the Wnt/ß-catenin signaling pathway in CNS cell fate specification.   We use zebrafish as a model organism, focusing on the regulation of Wnt/ß-catenin target genes in the CNS by a family of transcription factors called Tcf proteins.   Tcfs are required for ß-catenin to regulate transcription, and can act as repressors or activators of target genes depending on the state of Wnt signaling.   Three major questions are being addressed:   (1)   What cells in the CNS require ß-catenin/Tcf signaling?   (2)   What is the function of Tcf proteins in these cells?   (3)   Which genes are Lef/Tcf targets during CNS cell differentiation?

(1) What cells in the CNS require ß-catenin/Tcf signaling?   We are using several approaches to address this question.   We have generated transgenic zebrafish lines that express GFP under the control of a ß-catenin-responsive promoter, and are now characterizing GFP-expressing cell populations in the CNS and determining whether transgene expression in these regions also requires ß-catenin signals.   We have also cloned all of the existing tcf genes in zebrafish and are systematically examining their expression during CNS development.   Through these experiments we hope to identify novel ß-catenin/Tcf-responsive cell populations in the CNS.

(2) What is the function of Tcf proteins in responsive cells?   ß-catenin/Tcf activity could affect proliferation, cell fate, differentiation, or multiple pathways. To determine the necessity for Tcf function in individual cells, we have generated transgenic lines that expresse inducible constitutive repressors and activators of Tcf target genes.   We can activate the inducible promoters and follow the misexpressing cells in vivo to identify essential developmental roles played by ß-catenin/Tcf function in CNS development.   In addition, we are performing loss-of-function studies for tcf genes using either mutations or antisense gene knockdown.   Our goal is to uncover novel roles for ß-catenin/Tcf function in the development of specific CNS cell populations.

(3) What are the target genes?   Tcf function can lead to the repression or activation of downstream genes, but particular targets in the CNS are unknown.   We are using chromatin immunoprecipitation (ChIP) with our transgenic lines as well as specific Tcf antibodies to directly analyze candidate gene promoters as potential targets of Tcf   in the CNS.   The goal of this project is to identify Tcf target genes that are directly involved in cell fate determination and patterning of the CNS.

Expression of TOPdGFP, a live reporter for Wnt/ß-catenin signaling, in a 24-hour old zebrafish embryo.

 

References