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

Eryong Huang

Eryong Huang

Baylor College of Medicine

Department: Molecular & Human Genetics
Address: One Baylor Plaza, Rm. S416
Houston, TX 77030
Phone: (713) 798-4347
Fax: (713) 798-1021
Email: eh139881@bcm.tmc.edu
Web:

Education

M.S. Medical Sciences, China Medical University (1999); M.S. Molecular Biology, Purdue Univeristy (2002)

Honors

2003-2004 Fellowship of WM Keck Center of Computational and Structural Biology,
2004 Best Poster Award, SCBMB/CMB Research Conference

Research Topic

bZIP transcription factors and the development of Dictyostelium Discoideum

Research Description

The slime mould Dictyostelium discoideum has a characteristic uni-cellular to multi-cellular differentiation process that is induced by starvation. This is a highly regulated process and requires the cooperation of multiple signaling pathways. My aim is to identify all 19 bZIP transcription factors (TF) in the genome and study their function both experimentally and computationally. My plan is to knock out individual bZIPs and learn their phenotypes. DimA is a bZIP transcription factor that has been shown to be necessary for DIF-1 response, which is an alkyl hexanone produced by prespore cells and play an important role in stalk cell formation. However, the complexity of DIF-1 effects and the dimerization nature of bZIP transcription factors (TF) necessitate the studies on its dimerization partners in the whole genome. I have successfully knocked out 7 other bZIPs, and out of these 7 strains, dimB- shares similar phenotypic defects as dimA-. A great deal of work has been done on phenotyping dimB- mutant, and the results show that DimA and DimB could dimerize in vitro. My next plan is to do microarray phenotyping on the mutants. Differential analysis will be done to catch the candidate target genes of each individual bZIP. Dimerization pattern between each bZIP TFs will also be studied.

Selected Publications

Last edited on: March 17, 2008