Marie Winz
@mariewinz.bsky.social
170 followers 260 following 13 posts
RNA biologist at Johannes Gutenberg University Mainz, Germany: co-translational quality control - RNA modification - and beyond. Lab url: ak-winz.pharmazie.uni-mainz.de
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Reposted by Marie Winz
kusterlab.bsky.social
New preprint: We isolate peptide–RNA photo-crosslinks with tunable RNA chains from living cells for mass spec. This maps over 4,700 crosslinking sites across 744 proteins and offers the first glimpse into the RNA sequences in crosslinks by MS. Read here: doi.org/10.1101/2025...
Peptide-RNA photo-crosslinks with tunable RNA chain map protein-RNA interfaces
Photo-crosslinking mass spectrometry enables the identification of protein-RNA interactions in living cells, pinpointing interaction interfaces at single-amino acid resolution. However, current isolat...
doi.org
Reposted by Marie Winz
mariewinz.bsky.social
Thrilled to announce our #preprint on a new factor in the last line of defense in #translation quality control out on #bioRXiv! Spearheaded by fantastic PhD student @kaushikiyer.bsky.social, supported by Chloé Walter, Alina Kraft, Max Müller and Lena Tittel.
biorxivpreprint.bsky.social
Jlp2 is an RQC complex-independent release factor acting on aberrant peptidyl-tRNA, protecting cells against translation elongation stress https://www.biorxiv.org/content/10.1101/2025.09.04.673968v1
mariewinz.bsky.social
Curiously, Jlp2 acts not only on peptidyl-tRNA on large ribosomal subunits, but also on full monosomes. However, we also show that Jlp2 requires ribosome splitting for activity, suggesting that the monosomes represent re-assembled subunits. Read our preprint for full story!
mariewinz.bsky.social
Instead, we find that Jlp2 acts as a release factor enabling peptide release from ribosome-bound peptidyl-tRNA. We show that Jlp2 acts independently of the RQC complex and of other, known or expected release factors. Through peptide release, Jlp2 maintains cellular fitness in translation stress.
mariewinz.bsky.social
We identify yeast Jlp2 as a translation quality control factor that regulates CAT tailing upon RQC dysfunction, counteracting CAT tail-dependent protein aggregation. However, NOT by physically competing with or influencing abundance or function of Rqc2, the factor that catalyzes CAT tailing.
mariewinz.bsky.social
Stalled or collided ribosomes are split during quality control, leaving aberrant nascent peptides conjugated to tRNA bound to large ribosomal subunits. Those peptides are targeted by #RQC, and ubiquitinated and/or CAT tailed to facilitate degradation. If RQC fails, who comes to the rescue?
mariewinz.bsky.social
Thrilled to announce our #preprint on a new factor in the last line of defense in #translation quality control out on #bioRXiv! Spearheaded by fantastic PhD student @kaushikiyer.bsky.social, supported by Chloé Walter, Alina Kraft, Max Müller and Lena Tittel.
biorxivpreprint.bsky.social
Jlp2 is an RQC complex-independent release factor acting on aberrant peptidyl-tRNA, protecting cells against translation elongation stress https://www.biorxiv.org/content/10.1101/2025.09.04.673968v1
mariewinz.bsky.social
#proudPI moment yesterday, seeing my PhD student @kaushikiyer.bsky.social ace his talk at #EMBLProtein conference, presenting his work on new translation quality control factor Jlp2. Really did a great job holding up our lab's flag!!! 😄
Reposted by Marie Winz
kowaeva.bsky.social
Postdoc positions in structural biology of RNA processing complexes.

An ERC-funded position will dissect pre-mRNA processing pathways in the infective organism Trypanosoma brucei. An ANR-funded position will characterise large complexes in RNA modification.

Details: tinyurl.com/postdoc-RNA-...
Postdoc in Structural Biology of RNA processing complexes
Postdoctoral positions in structural biology of macromolecular complexes are available in the laboratory of Dr. Eva Kowalinski at the EMBL Grenoble, France. We are looking for highly motivated and amb...
tinyurl.com
mariewinz.bsky.social
4. Backtracked RNA can be polyadenylated (AAA) on the 3' end by the TRAMP complex. We speculate that AAA-marked nascent RNA could either be degraded or trigger reverse torpedo termination.

Although this work focuses on RNAPI, many findings apply broadly to RNAPs
mariewinz.bsky.social
3. We proposed an alternative model for torpedo termination, where a 5'→3' exonuclease trims the nascent RNA to RNAP boundaries, followed by backtracking-mediated cleavage.
mariewinz.bsky.social
2. We uncovered multiple mechanisms contributing to RNAPI transcription termination, including road-block termination, end-nucleolytic cleavage, and Rat1 torpedo termination.
mariewinz.bsky.social
Summary by Tomasz:
Some key takeaways:
1. The first experimental evidence supporting the model of immobilized RNAPs and spinning DNA—validated by experimental confirmation of theoretical predictions.
mariewinz.bsky.social
Paper alert 🚨 Check out our new paper about RNA polymerase I termination! Great collaboration with
Liz Petfalski, Katarzyna Grelewska-Nowotko and David Tollervey!
online yesterday in @CellReports! It took a while but finally come to life! t.co/5RPpxAhRvU
It was a pleasure to contribute!
https://www.cell.com/cell-reports/fulltext/S2211-1247(25)00096-8
t.co