Edda Schulz @eddaschulz.bsky.social · 20/01/2026⚒️ Through constructing a synthetic antisense locus, Verena then showed that gene repression, induced by antisense transcription can be stable for several days, when ESCs differentiate. 000
Edda Schulz @eddaschulz.bsky.social · 20/01/2026🧬 Till then found experimental evidence for promoter-repression by antisense transcription through a genome-wide analysis of nascent transcription during ESC differentiation. Here promoter-overlapping antisense pairs show mutual exclusive expression. 110
Edda Schulz @eddaschulz.bsky.social · 20/01/2026💻 Through extensive stochastic simulations 📈 Verena showed that (convergent) antisense transcription ➡️⬅️ can store stable memory, if antisense txn goes through the gene promoter and induces a stable repressed state. 100
Edda Schulz @eddaschulz.bsky.social · 17/11/2025📣 SAVE THE DATE Next X-inactivation meeting in Sapporo, Japan, 19-23 October 2026. Visit x-inactivation-meeting.org to join our mailing list. 🧬 speakers @dandergassen.bsky.social @marnieblewitt.bsky.social @heard65.bsky.social @crougeulle.bsky.social @sexchrlab.bsky.social @zhouqi1982.bsky.social 14018
Edda Schulz @eddaschulz.bsky.social · 06/10/2025🎯 Why It Matters: High Xist Levels are required for silencing the entire chromosome. 🎛️ Using CasTuner and enhancer deletions we show that Xist expression and silencing efficiency are dose-dependent 📈: reduced Xist RNA = impaired X-chromosome silencing 110
Edda Schulz @eddaschulz.bsky.social · 06/10/2025🔹 Phase 2 (High-Level Boost): Late TFs activate distal enhancers → They drive high Xist RNA levels needed for robust silencing. 100
Edda Schulz @eddaschulz.bsky.social · 06/10/2025The Xist switch has two distinct phases: 🔹 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. 110