Ph.D. Program in Structural and
Computational Biology and
Molecular Biophysics

Gadi Shaulsky

Gadi Shaulsky

Baylor College of Medicine

Department: Molecular and Human Genetics
Address: One Baylor Plaza Rm S930
Houston, TX 77030
Phone: (713) 798-8082
Fax: (713) 798-1021
Email: gadi@bcm.tmc.edu
Web: www.bcm.edu/db/db_fac-shaulsky.html

Education

B.Sc. Biology, Tel Aviv University, Israel (1985)
M.Sc. Biochemistry, Tel Aviv University, Israel (1986)
Ph.D. Cell Biology, The Weizmann Institute of Science, Rehovot, Israel (1991)
Postdoctoral: Department of Biology, UC San Diego

Honors

2005 Michael E. DeBakey, M.D., Excellence in Research Award

2000-2002 Basil O'Connor Starter Scholar (March of Dimes)

1994-1996 American Cancer Society (California branch) Senior Postdoctoral fellowship

1992-1993 Rothschild Fund fellowship for postgraduate studies.

Research Topic

Genetics and Functional Genomics of Dictyostelium Development

Research Description

Functional genomics

We have used microarrays to discover gene function in development (Booth et al., 2005), de-differentiation (Katoh et al., 2004), spore germination (Xu et al., 2004), and in drug resistance (Van Driessche et al. 2007). We also showed that the microarray is a good phenotyping tool for discovering epistatic relationships between six genes in the cAMP-dependent Protein Kinase regulatory pathway (Van Driessche et al., 2005). In collaboration with Dr. Kuspa, we are generating insertional mutations in most Dictyostelium genes and using the mutants to discover gene function by parallel phenotyping and by expression analysis.

Data Mining

We are collaborating with Dr. Blaz Zupan and his group at the University of Ljubljana in Slovenia to develop new concepts in genetic analysis. Together we have developed a tool that performs automated epistasis analysis http://genepath.org/. We also developed a tool that analyzes regulatory sequences in eukaryotic promoters http://dictybase.org/. We are currently developing a web tool that would access and analyze all of our microarray data.

The evolution of social behavior in Dictyostelium

Social organisms must deal with cheaters�individuals that reap the benefits of sociality without paying the costs. In Dictyostelium, some cells sacrifice themselves to benefit other cells that may be genetically different, providing a fertile ground for cheating. In collaboration with Drs. Strassmann and Queller at Rice University and Dr. Kuspa at BCM we found over 100 genes that participate in social interactions (Santorelli et al., 2008). We are using genetics to find and characterize additional genes that determine social decisions, find whether they are involved in rapid-evolutionary arms races, and test how cooperators resist cheating (Foster et al., 2004; Khare and Shaulsky, 2006).

bZIPs and the regulation of gene expression

A central signaling molecule in Dictyostelium is the Differentiation Inducing Factor (DIF-1) � A chlorinated alkylphenone. The mechanism of DIF signal reception is unknown. We isolated several strains that are insensitive to DIF-1 and identified dimA, which encodes a bZIP transcription factor (Thompson et al., 2004). We found another bZIP, dimB, that has overlapping functions with dimA (Huang et al., 2006). We are now mutating the remaining 17 bZIPs in the Dictyostelium genome to investigate their functions.

Selected Publications

Journal Covers

Lab Members

Current Graduate Students
Former Grad Students
Current Post Docs
Former Post Docs

Lab Photos

Shaulsky lab

Last edited on: September 22, 2009