We used rabies virus ๐พ to map how #psilocybin modifies long-range circuits ๐ง , revealing network-specific reorganization that we didnโt expect.
The full study is now online at Cell. @cp-cell.bsky.social
Paper ๐ www.cell.com/cell/fulltex...
Thread for a synopsis ๐
bsky.app/profile/alex...
05.12.2025 16:29
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Here, we develop a #CRISPR #epi-editing platform to probe #GeneRegulation in the brain. Silencing Neurexin-1 promoters in neurons affects downstream promoters & splicing patterns. Our data reveals transcriptional interference as key to shaping cell type-specific RNA isoforms of synaptic genes. ๐งช
16.09.2025 14:15
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The Gomez LAB
Hi Monica, may I be added to the feed? My neurobiology lab is at UC Berkeley an my lab website: www.andreagomezlab.com
15.09.2025 20:31
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mRNA 3โฒUTRs chaperone intrinsically disordered regions to control protein activity
More than 2,700 human mRNA 3โฒUTRs have hundreds of highly conserved (HC) nucleotides, but their biological roles are unclear. Here, we show that mRNAs with HC 3โฒUTRs mostly encode proteins with long intrinsically disordered regions (IDRs), including MYC, UTX, and JMJD3. These proteins are only fully active when translated from mRNA templates that include their 3โฒUTRs, raising the possibility of functional interactions between 3โฒUTRs and IDRs. Rather than affecting protein abundance or localization, we find that HC 3โฒUTRs control transcriptional or histone demethylase activity through co-translationally determined protein oligomerization states that are kinetically stable. 3โฒUTR-dependent changes in protein folding require mRNA-IDR interactions, suggesting that mRNAs act as IDR chaperones. These mRNAs are multivalent, a biophysical RNA feature that enables their translation in network-like condensates, which provide favorable folding environments for proteins with long IDRs. These data indicate that the coding sequence is insufficient for the biogenesis of biologically active conformations of IDR-containing proteins and that RNA can catalyze protein folding. ### Competing Interest Statement The authors have declared no competing interest. Pershing Square Foundation, https://ror.org/04tce9s05 G. Harold & Leila Y. Mathers Foundation National Institutes of Health, DP1GM123454, R35GM144046 Memorial Sloan Kettering Cancer Center, https://ror.org/02yrq0923, P30 CA008748
Very interesting looking work from @christinemayr.bsky.social lab
I'll put it at the top of my reading list, but the abstract already gave me some cool ideas.
#RNASky #RNABiology ๐งช
www.biorxiv.org/content/10.1...
07.07.2025 21:23
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In this time of chaos - something good! We are excited to share our final (or near final) speaker list for the 3rd UCSF Full Circle Symposium 4/3-4/4 to highlight Native biologists! Please share the word and register to attend the webinar in person! More info: qbi.ucsf.edu/full-circle-...
05.03.2025 20:59
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Yesss! #RNAsky
26.02.2025 17:33
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Our latest study is available as a preprint.
We show that psychedelics induce subtle changes in gene expression but robust changes in alternative splicing lasting at least one month, suggesting that alternative splicing may represent a general mechanism for prolonged plasticity in neurons. #RNAsky
17.01.2025 05:01
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Thank you to @mayoonthebrain.bsky.social & @indigenerd.bsky.social for keynoting, & Tristan McClure-Begley, Katherine Bonson, Xiangmin Xu, Daniele Piomelli, Adrian Preda, and Kate Lawson, Steve Grant, & all attendees, for participating in this #psychedelic symposium @UCIrvine yesterday!
19.11.2024 20:53
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Stimulating discussions. Many take-aways. Thanks @svmahler.bsky.social
19.11.2024 21:54
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