Iana V. Kim
@ianakim.bsky.social
330 followers 500 following 29 posts
Postdoctoral researcher in the Sebe-Pedros and Marti-Renom Labs at CRG. Transposable elements enthusiast, passionate about piRNAs, 3D genomes, and Star Trek 🖖
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ianakim.bsky.social
Really grateful to see our work featured by @quantamagazine.bsky.social in this piece on the evolution of genome regulation. Huge thanks to @philipcball.bsky.social for such a beautifully written article.
philipcball.bsky.social
I adored writing this piece. It brings together several of the things preoccupying me right now, like chromatin organization and gene regulation. There's so much more to be said on that. Also, these marine critters look gorgeous.
www.quantamagazine.org/loops-of-dna...
Loops of DNA Equipped Ancient Life To Become Complex | Quanta Magazine
New work shows that physical folding of the genome to control genes located far away may have been an early evolutionary development.
www.quantamagazine.org
Reposted by Iana V. Kim
arnausebe.bsky.social
A thoughtful and beautifully written @quantamagazine.bsky.social article about genome regulatory innovation at the origin of animals. Featuring some of our work and highlighting key open questions. Thanks to @philipcball.bsky.social for this fantastic piece.
philipcball.bsky.social
I adored writing this piece. It brings together several of the things preoccupying me right now, like chromatin organization and gene regulation. There's so much more to be said on that. Also, these marine critters look gorgeous.
www.quantamagazine.org/loops-of-dna...
Loops of DNA Equipped Ancient Life To Become Complex | Quanta Magazine
New work shows that physical folding of the genome to control genes located far away may have been an early evolutionary development.
www.quantamagazine.org
Reposted by Iana V. Kim
rafeeque.com
🧵5 Top Free Alternatives to BioRender for Scientific Illustrations!

These five websites offer free scientific illustrations for biologists. Great for presentations, research papers and other research communication needs.

Save and share the post!
Reposted by Iana V. Kim
seanamontgomery.bsky.social
Updating my intro slides with this fantastic figure now! (And maybe I'll add an extra dashed line for my beloved bryophytes)
strassert.bsky.social
Happy to have contributed to this great article: #Protist genomics: key to understanding eukaryotic evolution. Congrats Alexandra Schoenle et al. #ProtistsOnSky
authors.elsevier.com/sd/article/S...
Reposted by Iana V. Kim
Reposted by Iana V. Kim
kazu-maeshima.bsky.social
Our new paper is out@ScienceAdvances👇
www.science.org/doi/10.1126/...
🧬Our Repli-Histo labeling marks nucleosomes in euchromatin and heterochromatin in live human cells.
🔍 @katsuminami.bsky.social et al. have developed a chromatin behavior atlas within the nucleus. 1/2
ianakim.bsky.social
Thank you so much, Lorenza :)
ianakim.bsky.social
Thank you, Isabel!
ianakim.bsky.social
Thank you very much, Thibaut!
ianakim.bsky.social
Thank you, Paula :)
ianakim.bsky.social
thank you, Juan!
ianakim.bsky.social
thanks a lot, Claus! :)
ianakim.bsky.social
thank you, Dima!
ianakim.bsky.social
There’s much more to explore in the paper—so dive in! It also opens exciting questions for future research: What is the role (if any) of loop extrusion in the formation of these structures? Are these loops dynamic across development/cell types? When did insulating sequence elements evolved?
ianakim.bsky.social
This is our (current/tentative) model for the early evolution of animal chromatin architecture.
ianakim.bsky.social
Finally, in unicellulars, chromatin architecture is “passively” defined by active/repressive chromatin states, without evidence of sequence elements or specific factor binding. See for example co-segregating repressive domains in Sphaeroforma, highly enriched in TEs:
ianakim.bsky.social
In sponges we do not identify loops, despite the existence of distal enhancers. We hypothesize this could be explained by the relative proximity (<10Kb) of these enhancers to the closest TSS. What we do observe are prominent chromatin jets/fountains, as also recently described in other species.
ianakim.bsky.social
In the cnidarian Nematostella, we observe multiple enhancer-promoter loops, including some very distal ones (1Mb). Interestingly, here loops show a characteristic one-sided stripe, which may suggest active extrusion (?).
ianakim.bsky.social
In placozoans, we observed promoter-promoter hubs, highly conserved across two distantly related species.
Not all genes participate in these hubs, only those containing a sequence motif found in TIR sequences of a Mutator DNA transposon, with highly conserved insertions across all placozoans.
ianakim.bsky.social
What proteins are involved in forming these loops? CTCF is absent in non-bilaterians. Using chromatin proteomics and DAP-seq, we identified two ctenophore-specific zf-C2H2 proteins that we called Ctenophore Tethering Element Proteins, which also cannot bind methylated sites.
ianakim.bsky.social
The most unexpected finding is the presence of chromatin loops genome-wide in ctenophores, cnidarians and placozoans. Nothing in unicellular holozoans. See an example of the beautiful regulatory landscapes in Mnemiopsis, with thousands of loops connecting enhancers and promoters.
ianakim.bsky.social
To interpret these maps we first generated new, chromosome-scale assemblies for Capsaspora, Mnemiopsis and Ephydatia, reassembled pre-existing scaffolds for others species, and profiled diverse linear epigenomic marks (hPTMs, accessibility, methylation).
ianakim.bsky.social
To reconstruct the evolutionary history of animal regulatory genomes, we used Micro-C to explore 3D genomes across 7 lineages (9 species in total!) spanning the origin of Metazoa.