Silvia Ramundo

@sramundo.bsky.social

Curious scientist leading a research team mainly working on organelle biology and biotechnology: we study -and often “torture”- chloroplasts to understand how they do their magic ;) https://www.oeaw.ac.at/gmi/research/research-groups/silvia-ramundo

I often find people who think as I do. Like this student in my microbiology course at the University of Canterbury. I talked about cotransduction in microbial genetics, and then bacteriophage therapy to fend off antibiotic resistant bacteria. The student drew this in class, and showed it to me.

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Did you ever want to sequence that one interesting cell you observed in your microscopy experiment? We have a new pre-print out today that describes a genetic barcoding method, Waldo, to perform live-cell imaging and single-cell sequencing on the same single cells. www.biorxiv.org/content/10.6...

Linking live-cell imaging to single-cell sequencing using genetic barcoding

Linking cellular phenotype to genotype and gene expression is a central goal in biomedical research. Live-cell imaging captures dynamic cellular phenotypes, whereas single-cell sequencing measures gen...

biorxiv.org

A big thank you to the one and only @harmitmalik.bsky.social for such a thoughtful and memorable gift and for an unforgettable collaboration at Fred Hutch’s Basic Scuences Division @basicsci.fredhutch.org ! We love you, Harmit! ♥️

Harmit Singh Malik@harmitmalik.bsky.social · 2d ago

Celebrating the 3 amigos on their paper identifying metazoan HJURP orthologs: @jeremyahollis.bsky.social (Malik/ Campbell labs), @irinakitop.bsky.social (Nic Lehrbach lab), Jason Stonick (Cecilia Moens lab). @basicsci.fredhutch.org Mugs: sciencegrit.com Paper: www.science.org/doi/10.1126/...

Challenge 3: functional integration. Rather than always inventing new genetic programs, nascent organisms often co-opt ancestral modules, turning environmentally induced cell states into spatially deployed cell types (e.g., Volvox regA, derived from a stress-response gene).

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Challenge 2: the Darwinian threshold. Groups need a life cycle before they can evolve one, a classic chicken-and-egg problem. The way out: life cycles can be scaffolded "for free," either by the environment (e.g., floods dispersing cells) or by physics (packing stress fracturing snowflake yeast).

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Challenge 1: forming groups. Across yeast, algae, bacteria and holozoans, lab evolution shows group formation arises fast (within 100–750 generations) and convergently, often through simple mutations like loss of ACE2 in snowflake yeast.

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Multicellularity has evolved at least 45 times in eukaryotes alone, plus additional origins in bacteria and archaea. But how does it actually happen? We organize the paper around three perceived challenges: group formation, becoming a Darwinian individual, and functional integration.

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I'm not going to lie, this review puts the various challenges driving multicellularity very elegantly. For anyone excited about this field, this review is a must read. And damn this video is very very nice ! Congrats Will, Kai and Ozan.

Will Ratcliff@wcratcliff.bsky.social · 4d ago

Out today in @nature.com: our review on how single cells evolve into multicellular organisms. With Ozan Bozdag, @kaitong25.bsky.social, Peter Yunker, and @matthewherron.bsky.social. rdcu.be/9ZuiKow9twKa For an overview, check out the video below.

Then came the evolutionary surprise. HREZ and Tm-2² are not close relatives. They sit in distinct branches of the plant NLR immune receptor family. Yet both recognize tobamovirus movement proteins. Two evolutionary paths, one viral target. (5/9)

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Whenever I see this poster, made to tease a visiting student in our lab, I can’t help but smile! Looking back on my own PhD days, even the toughest moments make me laugh now. And for the record, that student is now happily doing a postdoc! So there’s hope, even on those “I’m quitting science” days 🙃

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