William Garland

@willgarland.bsky.social

RNA decay, RNA sorting, transcriptional regulation Aarhus University, Denmark 🇩🇰

How do cells sort which RNAs to keep or destroy? New preprint from THJ, Brenneke and Plaschka labs shows that export and decay machineries (TREX2/PAXT) both recognise UAP56-bound RNAs. Whether they’re exported or degraded depends on where in the nucleus this happens. www.biorxiv.org/content/10.1...

Molecular basis of polyadenylated RNA fate determination in the nucleus

Eukaryotic genomes generate a plethora of polyadenylated (pA+) RNAs, that are packaged into ribonucleoprotein particles (RNPs). To ensure faithful gene expression, functional pA+ RNPs, including prote...

biorxiv.org

“Today Google is launching an AI co-scientist, a new AI system built on Gemini 2.0 designed to aid scientists in creating novel hypotheses and research plans. AI co-scientist is a collaborative tool to help experts gather research and refine their work” blog.google/feed/google-...

We’re launching a new AI system for scientists.

Today Google is launching an AI co-scientist, a new AI system built on Gemini 2.0 designed to aid scientists in creating novel hypotheses and research plans. Researchers…

blog.google

We are pleased to announce registration for RNA 2025 - the 30th Annual Meeting of the RNA Society - is now open! www2.rnasociety.org This year’s meeting will be held at the beautiful Town and Country Resort & Convention Center in sunny San Diego, California, USA from May 27th - June 1st, 2025.

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Is there a common contaminant database for proximity labelling-MS data? I see that the CRAPome has a section for proximity-dependent biotinylation but it is limited to human cells. I keep seeing the same nonsense proteins enriched in mTurbo-experiments and would love to know if this is common crap.

Cell lines are frozen, chrome tabs, spreadsheets and documents have been closed. All done for this year ✌️ Back in Derbyshire and busy making sausage rolls. It's been a productive year, but i'm in dire need of a break.

📢 Latest publication from the lab! We explore how cells manage the excess pA− RNAs generated by pervasive transcription. While the NEXT complex usually takes charge, in its absence, a network of tailing enzymes, export factors, and exonucleases steps in to modify and degrade these RNAs.

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New preprint! Great to be a part of this collaboration with the Cusack and Kadlec groups. Here we have uncovered the cryo-EM structure of the snRNA export complex, revealing how PHAX bridges CBC-bound RNA to CRM1-RanGTP, committing it to export. www.biorxiv.org/content/10.1...

Structural basis for the synergistic assembly of the snRNA export complex

The nuclear cap-binding complex (CBC) and its partner ARS2 play crucial roles in regulating Pol II transcript fate through mutually exclusive interactions with RNA effectors. One such effector, PHAX, ...

biorxiv.org

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Check it out! The RNA Society 2025 Meeting Site is now live! Registration will open in January RNASociety Note the fabulous artwork by former EmoryBCDB student Dr. Carly Lancaster- make your plans now to join us in San Diego May 27-June 1, 2025

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