Ana Tufegdzic Vidakovic
@anatv.bsky.social
400 followers 290 following 12 posts
Group Leader at MRC Laboratory of Molecular Biology. Transcription, RNA Polymerase II, Ubiquitin
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anatv.bsky.social
@mrclmb.bsky.social MRC LMB is looking for a new group leader in Chemical/Synthetic Biology. Come and join us in this fantastic institute! Core funding, amazing science all around you and great collaborative colleagues are just some of the highlights. Please share the news!
philholliger.bsky.social
We are looking to recruit a tenure track group leader in the field of Chemical/Synthetic Biology (in the broadest sense) to lead a research program within the Division of Protein & Nucleic Acid Chemistry ( www.jobs.ac.uk/job/DNW809/r... ) at the MRC Laboratory of Molecular Biology (LMB).
Research Group Leader in Chemical/Synthetic Biology at MRC Laboratory of Molecular Biology
Start your UK & international job search for academic jobs, research jobs, science jobs and managerial jobs in leading universities and top...
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anatv.bsky.social
Looking forward to presenting at the Cambridge RNA club again! If you are interested in gene regulation and around Cambridge, stop by!
cambridgerna.bsky.social
Ever wondered how RNA polymerase II gears up to tackle obstacles on DNA?
Turns out, cells have a preparation pathway, and it’s way cooler than we imagined!
Join us and @anatv.bsky.social on June 26th to discover how Pol II gets battle-ready! 💥🧪 #RNAClub
anatv.bsky.social
The first PhD student of our lab, 5'-Ivan Shlamovitz, has passed his viva with flying colours! What a special moment! The whole lab (and many friends at the LMB) are proud! 👏😁
anatv.bsky.social
We conclude that ARMC5 and Integrator phosphatase work in parallel to monitor the quantity and quality of Pol II complexes before they are licenced to enter elongation.
anatv.bsky.social
We conduct a synthetic lethality mini-screen and identify Integrator phosphatese compensates for the loss of ARMC5! When both Integrator phosphatase and ARMC5 are missing, excessive Pol II enters early elongation, but many of these are transcription-incompetent and fail to reach gene ends.
anatv.bsky.social
Loss of ARMC5 causes profound accumulation of Pol II both off-DNA and at gene beginnings, but not in gene bodies. Something else is preventing all this excess Pol II at initial stages of transcription to proceed into elongation. What is it?
anatv.bsky.social
But why would cells ubiquitylate and destroy promoter-proximal Pol II? We find that ARMC5 targets "defective" Pol II complexes! So what happens to transcription if this pathway is lost?
anatv.bsky.social
We find this new Ub Pol II form specifically comes from the promoter-proximal zone, leads to Pol II degradation, and identify the E3 ligase responsible is ARMC5-CUL3!
anatv.bsky.social
It all started when we observed a strange new form of ubiquitylated Pol II on gels, that looked and behaved very different than the only well-characterized Ub Pol II form we knew about at the time - elongation-stalled Pol II (more on that subject in our 2020 paper)

www.cell.com/cell/fulltex...
Regulation of the RNAPII Pool Is Integral to the DNA Damage Response
Control of the pool of available RNA polymerase II shapes how cells respond to UV stress and the efficacy of the resulting damage response.
www.cell.com
anatv.bsky.social
Congratulations Marta 👏👏👏!