Daniel MK Lee

@dannimklee.bsky.social

MSCA postdoctoral fellow at Max Planck Institute for Molecular Genetics. PhD alumnus at Institut Curie. Epigenetics, DevBio, Transcriptional regulation, Organoids

Happily, our fly stock room has been restored to 18°C and the labs are now a chilly 30°C. We will see how the hot week ahead progresses.

Bardin Lab@bardinlab.bsky.social · 2mo ago

How HOT is TOO HOT to work in lab? 33°C? 35°C? 37°C? Our aircon in the BDD @institutcurie.bsky.social , which hasn't worked well for years, is now dead. This is our "18°C" room for important fly stocks (now at 29°C!). It is 33°C in the labs today, and will only increase over the next 6 days!

I am extremely honored and grateful to see our work featured on PreLights @prelights.bsky.social. If you want a quick dive into how acute loss of PRC2 impacts TLS formation, check out this excellent breakdown by María @mariamafau.bsky.social. I had a great time discussing the work with her.🔬👇

María Mariner@mariamafau.bsky.social · 3mo ago

🚨Happy to share a new PreLight covering the latest #preprint by the Meissner lab (@molgen.mpg.de) on acute SUZ12 degradation during TLS formation. A work brilliantly executed by @dannimklee.bsky.social et al. Get to know more about him and his work here ⤵️ prelights.biologists.com/highlights/t...

Big congrats to Julia! Besides doing amazing science, she has always been a super kind, supportive colleague. I can not wait to hear more about her cool work and so so happy for her for her new journey!

FMI science@fmiscience.bsky.social · 4mo ago

In this interview, @juliabatki.bsky.social, FMI’s newest group leader, reflects on the early curiosity that drew her to science, why FMI is the right home for her lab, how studying cell clearance could help us understand disease, and her love of improv. www.fmi.ch/news-events/...

🧵 CTCF is essential for embryonic development, but why has remained unclear. By combining gastruloids with a temporal degron system, we uncovered a surprising dual function — and it changes how we think about CTCF's role in development. 1/8 www.biorxiv.org/content/10.6...

A dual role for CTCF in development

CTCF is an essential DNA binding protein whose absence leads to embryonic lethality. CTCF is primarily known for its role in 3D genome organization where its N-terminal domain interacts with cohesin to anchor chromatin loops. How CTCF facilitates proper embryonic development remains unclear, necessitating temporal control to resolve its stage-specific functions. By combining gastruloids, an in vitro model of embryonic development, with a degron system to rapidly deplete CTCF at defined timepoints, we show that early CTCF depletion impairs early gastruloid morphogenesis. Surprisingly, ATAC-seq and time-resolved RNA-seq revealed that differentiation was unaffected. CTCF binding is strongly enriched at promoters of downregulated genes. Re-expression of a CTCF variant with an N-terminal truncation, incapable of looping, was sufficient to rescue the expression of CTCF-promoter bound genes and the defects in morphogenesis. However, extended culture (up to 168 hours) of gastruloids reconstituted with N-terminal truncated CTCF led to their collapse. Our work shows that CTCF has a dual function in early mammalian development: at early stages CTCF regulates developmentally important genes through promoter binding, while at later stages its looping function is required for correct development. ### Competing Interest Statement The authors have declared no competing interest. European Research Council, https://ror.org/0472cxd90, 637587, 865459 Dutch Research Council, https://ror.org/04jsz6e67, 016.161.316, VI.C.222.049 Dutch Cancer Society, https://ror.org/0368jnd28, N/A

biorxiv.org

Are you a DNMT3 enthusiast wondering how they achieve specificity at CpG islands during development? And why is DNMT3B specifically required for methylation on the inactive X? We set out to dissect the mechanism, now published in Genes & Development genesdev.cshlp.org/content/earl... [1/12]

Chromatin binding and N-terminal domains of DNMT3B1 confer specificity for developmentally regulated CpG island methylation

A biweekly scientific journal publishing high-quality research in molecular biology and genetics, cancer biology, biochemistry, and related fields

genesdev.cshlp.org

Very excited to share our new Molecular Cell paper on missense mutations in Polycomb genes and how they can disrupt chromatin regulation to drive neurodevelopmental disorders. A huge thank you to everyone involved, and to our amazing collaborators! www.cell.com/molecular-ce...

Unbalanced chromatin binding of Polycomb complexes drives neurodevelopmental disorders

Borges, González-Blanco, Arigela, et al. report new missense mutations in the PRC1 genes RNF2 and RING1 in individuals with neurodevelopmental disorders. Functional dissection of a deleterious variant...

cell.com

During germline epigenetic reprogramming, Polycomb must be restricted in the gametes to ensure proper genome regulation in the fertilized embryo. 2 must-read papers assess what happens when Ezhip (Polycomb antagonist) is lost. They come to highly similar conclusions and should be read in tandem 1/4