Anamaria Elek

@aelek.bsky.social

Postdoc @ Kaessmann and Sasse labs @zmbh.uni-heidelberg.de Previously PhD @ Sebé-Pedrós lab @crg.eu Interested in regulatory genomics, evolution, machine learning, and especially the combination of all of the above. https://anamaria.elek.hr/

Huge congrats from our whole lab to Sir David Attenborough on his 100th birthday!!! 🎉🥳❤️ I had the honor of meeting him - and being interviewed by him - in 2013 for his BBC documentary "Rise of Animals: Triumph of the Vertebrates", which featured part of our work.

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Excited to share the preprint from my main postdoc project! It’s been a long journey—huge thanks to everyone who made it possible, especially @leticiarm1618.bsky.social for being the best collaborator one could ask for, and the amazing @kaessmannlab.bsky.social lab for the invaluable support!

Kaessmann Lab@kaessmannlab.bsky.social · 10mo ago

We are thrilled to share our new preprint entitled “The origin and molecular evolution of the mammalian liver cell architecture” www.biorxiv.org/content/10.1...

BCA is a project to look out for — charting the diversity of cell type transcriptomes across the tree of life. Not only will it empower evolutionary studies, but also drive advances in biotechnology, biomedicine, and ecology. Kudos to the relentless, meticulous, and persistent team doing this work!

Arnau Sebé-Pedrós@arnausebe.bsky.social · 11mo ago

Happy to share the Biodiversity Cell Atlas white paper, out today in @nature.com. We look at the possibilities, challenges, and potential impacts of molecularly mapping cells across the tree of life. www.nature.com/articles/s41...

I am very happy to have posted my first bioRxiv preprint. A long time in the making - and still adding a few final touches to it - but we're excited to finally have it out there in the wild: www.biorxiv.org/content/10.1... Read below for a few highlights...

Decoding cnidarian cell type gene regulation

Animal cell types are defined by differential access to genomic information, a process orchestrated by the combinatorial activity of transcription factors that bind to cis -regulatory elements (CREs) to control gene expression. However, the regulatory logic and specific gene networks that define cell identities remain poorly resolved across the animal tree of life. As early-branching metazoans, cnidarians can offer insights into the early evolution of cell type-specific genome regulation. Here, we profiled chromatin accessibility in 60,000 cells from whole adults and gastrula-stage embryos of the sea anemone Nematostella vectensis. We identified 112,728 CREs and quantified their activity across cell types, revealing pervasive combinatorial enhancer usage and distinct promoter architectures. To decode the underlying regulatory grammar, we trained sequence-based models predicting CRE accessibility and used these models to infer ontogenetic relationships among cell types. By integrating sequence motifs, transcription factor expression, and CRE accessibility, we systematically reconstructed the gene regulatory networks that define cnidarian cell types. Our results reveal the regulatory complexity underlying cell differentiation in a morphologically simple animal and highlight conserved principles in animal gene regulation. This work provides a foundation for comparative regulatory genomics to understand the evolutionary emergence of animal cell type diversity. ### Competing Interest Statement The authors have declared no competing interest. European Research Council, https://ror.org/0472cxd90, ERC-StG 851647 Ministerio de Ciencia e Innovación, https://ror.org/05r0vyz12, PID2021-124757NB-I00, FPI Severo Ochoa PhD fellowship European Union, https://ror.org/019w4f821, Marie Skłodowska-Curie INTREPiD co-fund agreement 75442, Marie Skłodowska-Curie grant agreement 101031767

biorxiv.org

🧬🔍How can enhancers achieve tissue-specific activity? We use MPRAs of synthetic enhancers to derive interpretable rules on TFBS arrangement 🚦 and discover that negative synergies drive specificity in hematopoiesis 🩸. Shoutout to @Robert Frömel & @larsplus.bsky.social for leading this work 🦹🦸.

Lars Velten@larsplus.bsky.social · last yr.

Out in Cell @cp-cell.bsky.social: Design principles of cell-state-specific enhancers in hematopoiesis 🧬🩸 screen of fully synthetic enhancers in blood progenitors 🤖 AI that creates new cell state specific enhancers 🔍 negative synergies between TFs lead to specificity! www.cell.com/cell/fulltex... 🧵

Out in Cell @cp-cell.bsky.social: Design principles of cell-state-specific enhancers in hematopoiesis 🧬🩸 screen of fully synthetic enhancers in blood progenitors 🤖 AI that creates new cell state specific enhancers 🔍 negative synergies between TFs lead to specificity! www.cell.com/cell/fulltex... 🧵

Design principles of cell-state-specific enhancers in hematopoiesis

Screen of minimalistic enhancers in blood progenitor cells demonstrates widespread dual activator-repressor function of transcription factors (TFs) and enables the model-guided design of cell-state-sp...

cell.com

New preprint from the @arnausebe.bsky.social lab! 💐 Here @crisnava.bsky.social, @seanamontgomery.bsky.social & collaborators develop a novel ChIPseq protocol, and demonstrate its huge potential to study the evolution of chromatin function and regulation across the eukaryotic tree of life.

Figure 1 from the paper, with two panels. Panel a shows a schematic cladogram of the eukaryotic tree of life with an adjacent table showing the presence/absence of various histone post-translational modifications in various lineages. Panel b is a summary of the multiplexing strategy for ChIP-seq experiments developed in the paper.
bioRxiv Evolutionary Biology@biorxiv-evobio.bsky.social · last yr.

Diversity and evolution of chromatin regulatory states across eukaryotes https://www.biorxiv.org/content/10.1101/2025.03.17.643675v1