Really happy to share that our preprint is now published in @narjournal.bsky.social! 🎉
Posts by Thomas Balan
now published at BMC Biology!
rdcu.be/fdITD
There are Science papers and then there are *I just dropped and shattered my mug of coffee Usual Suspects style* Science papers www.science.org/doi/10.1126/...
✍️ The @sandraduharcourt.bsky.social Lab published a new article
📖 Genome Biology
📃 A H3K27me3 reader complex couples H3K27me3 accumulation to nascent transcription of transposable elements in Paramecium
🔗 link.springer.com/article/10.1...
Merci Raphaël !!
Thanks Max!
Thank you Bassem!
Thank you Peter!
Thanks Ralf!
First first-author paper out! 🎉
We show that the classically repressive mark H3K27me3 can be linked to active transcription through a newly identified reader complex 🤯
Really grateful to everyone involved in this project during my PhD!
Thread below 👇
Germ cells have their own versions of core transcription factors and fertility depends on them.
We're hiring a PhD student to figure out how! 📢
Fly genetics + proteomics + genomics. Fully funded.
Aarhus University 🇩🇰
Deadline May 1 👇
Please share with anyone who might be interested!
Our work on chromatin evolution in brown algae is finally out!
This is also my first "co-first author" paper!! I’m excited to share what we found 👇
Excited to share our new preprint exploring how Paramecium achieves diverse flow functions, i.e. feeding and swimming, simultaneously. This work was spearheaded by our ExM expert, PhD student Daphne Laan @daphnelaan.bsky.social :
www.biorxiv.org/content/10.6...
Excited to announce the upcoming Jacques Monod Conference on the mechanistic and evolutionary basis of programmed DNA elimination (Sept 21–25, 2026):
cjm.sb-roscoff.fr/en/conferenc...
Organized by @laurarossevo.bsky.social and myself.
How does the piRNA pathway solve the self vs. non-self problem? 🧬
Since piRNAs come from single-stranded RNA, how does the cell choose the right ones? For years, "piRNA clusters" were seen as THE privileged source. But are they really special and earmarked for biogenesis? (1/19)
A Naïve RNA Sampling Core Enables Adaptive piRNA Specificity Against Transposable Elements www.biorxiv.org/content/10.64898/2026.02...
Happy to begin the year with the publication of a Journal Club article - Programmed ‘DNA splicing’ removes transposons from genes.
rdcu.be/eXBym
Out today, our take on 6-methyladenine #6mA evolution in Eukaryotes @natgenet.nature.com. We asked a simple question, is really DNA 6mA common across the eukaryotes? The answer is "yes" if you're a unicellular eukaryote 🦠, not so if you're multicellular 🐝🌱🍄. www.nature.com/articles/s41... 1/9
Excited to share our new preprint on BioRxiv!
A collaborative effort spanning many years and several labs to uncover what the germline chromosomes of Paramecium really look like. 🔗 www.biorxiv.org/content/10.1...
1/5
Congrats Andreas!!
Lab’s first paper is out!! We show the first structures of #Asgard #chromatin by #cryo-EM 🧬❄️
Asgard histones form closed and open hypernucleosomes. Closed are conserved across #Archaea, while open resemble eukaryotic H3–H4 octasomes and are Asgard-specific. More here: www.cell.com/molecular-ce...
BMP signaling-dependent dorsal-to-ventral gradient of PAX3/7 transcriptional activity revealed by the P34::tk::LacZ reporter. Left: expression patterns of neural progenitor (NP) and interneuron (IN) TF markers in the developing spinal cord. Right: Immunostaining for β-galactosidase (β-gal; red/grey), GFP (blue/grey) and either OLIG3 (green/grey) or pSMAD1/5/9 (green/grey) on transverse sections of E9.0 (bottom) and E9.5 (top) P34::tk::LacZ; Pax3+/GFP spinal cords at brachial level. Black and white panels show magnified views of the boxed region.
How do pleiotropic TFs generate organized diversity in developing tissues? @spinalorga.bsky.social shows that PAX3 & PAX7 organize #SpinalCord by acting as both repressors & pioneer activators, regulated by #morphogens to ensure precise neural subtype specification @plosbiology.org 🧪 plos.io/4qumsla
Thanks Max!!
@ijmonod.bsky.social @i2bcparissaclay.bsky.social @frm-officiel.bsky.social @EUR_G.E.N.E @upcite.bsky.social
This is part of my PhD work that I recently concluded in the lab of @sandraduharcourt.bsky.social 🎓 🎓
Huge thanks to everyone who contributed to this story (Mélanie, Marc & Valério, who are co-authors with me on this project !) as well as all collaborators for their dedication and insights. 🎉
By revealing how condensin I assists a domesticated transposase in sculpting the somatic genome, this work opens the door to exploring how genome organisation shapes DNA elimination in Paramecium 🤩
👉 To conclude, we show that condensin I physically and functionally interacts with PiggyMac, thus highlighting a strong interaction between the two machineries.
🧬 We demonstrate that this new development-specific complex is essential for DNA elimination and the establishment of H3K9me3 & H3K27me3 patterns during development, fully phenocopying PiggyMac depletion.
🧪Using TurboID proximity labelling, we identified condensin I subunits among the closest interactors of the PiggyMac endonuclease, leading to the identification of a development-specific condensin I complex
During Paramecium development, 30% of the germline genome, including TEs, is precisely eliminated to form a functional somatic genome.
The endonuclease PiggyMac and its partners catalyse this process, but how they are targeted to DNA is unknown. (see doi.org/10.1002/wrna... for more)