Interested in quantitative biology, gene regulation, epigenetics, system biology and X-chromosome inactivation.
https://www.molgen.mpg.de/schulz-lab
🎛️ Using CasTuner and enhancer deletions we show that Xist expression and silencing efficiency are dose-dependent 📈: reduced Xist RNA = impaired X-chromosome silencing
🎛️ Using CasTuner and enhancer deletions we show that Xist expression and silencing efficiency are dose-dependent 📈: reduced Xist RNA = impaired X-chromosome silencing
→ They drive high Xist RNA levels needed for robust silencing.
→ They drive high Xist RNA levels needed for robust silencing.
🔹 Phase 1 (Binary ON/OFF): Early TFs target proximal regulatory elements
→ They sense X-chromosome number (XX vs XY) to trigger initial Xist upregulation—ensuring female-specific activation.
🔹 Phase 1 (Binary ON/OFF): Early TFs target proximal regulatory elements
→ They sense X-chromosome number (XX vs XY) to trigger initial Xist upregulation—ensuring female-specific activation.
This is done by the Xist gene, a master regulator that coats one X in RNA.
But how does Xist KNOW when to turn on—and only in females?
🔬 Our new study reveals a two-step regulatory logic that decodes sex and development.
This is done by the Xist gene, a master regulator that coats one X in RNA.
But how does Xist KNOW when to turn on—and only in females?
🔬 Our new study reveals a two-step regulatory logic that decodes sex and development.