Julia Zeitlinger, PhDAssistant Investigator, Stowers Institute for Medical
Research
Assistant Professor of Pathology and Laboratory Medicine
Division
of Cancer & Developmental Biology
Ph.D.: 1999, European Molecular Biology Laboratory in Heidelberg,
Germany
Postdoctoral: Whitehead Institute for Biomedical Research, M.I.T
Email: jbz @ stowers-institute.org
Zeitlinger
Lab web site
Publications: Click here for list of publication from PubMed
Ph.D. students are welcome. Contact me for more info.
Human disease is frequently associated with aberrant signal
transduction components, DNA-binding transcription factors and
chromatin modifying enzymes, yet how these components regulate
specific biological outcomes is largely unknown. There is therefore
a critical need to understand how regulatory proteins affect
global gene expression and cellular behavior in a context-specific
manner.
The long-term goal of our research is to identify predictive rules by which gene expression programs are established in an organism and apply them to human disease. It is known that gene expression programs are specified by signal transduction pathways that are activated by signals from neighboring cells during development. How these signal transduction pathways regulate gene expression is highly context-dependent. Based on current knowledge, gene regulation depends on two principles, combinatorial regulation and (epigenetic) cellular memory. We are studying both principles by combining the power of classical Drosophila genetics with that of state-of-the-art genomics techniques.
One of the techniques frequently used in the lab to globally
map protein-DNA interactions is ChIP-chip and ChIP-seq analysis.
In this technique, chromatin immunoprecipitation (ChIP) is performed
using antibodies against a DNA-binding protein. The DNA to which
the protein is bound is then identified by either microarray
analysis (chip) or sequencing (seq). For example, we have applied
this technique to study the dorso-ventral axis specification
in Drosophila, which involves the transcription factors Dorsal,
Twist and Snail.
