long-lived species and humans living 100+ years are known to have increased DNA repair capacity
but how DNA repair could be boosted to extend human lifespan is largely unknown
our research in Nature Aging today proposes a target to enable such a boost: the DREAM complex
Targeting DNA damage in ageing: towards supercharging DNA repair, read now our latest article in @NaturePortfolio Nature Reviews in Drug Discovery. @ArBujarrabal@George_Garinis Paul Robbins Jan Vijg @CECAD_@UKKoeln
Free access to the article here:
https://t.co/T2rX40orEC
Excited to announce our paper in @NAR_Open: "Distinct #DNARepair mechanisms prevent #Formaldehyde toxicity during development, reproduction, and aging." https://t.co/RE3P7XPgSZ
Read our new paper about different neuronal aging rates! 🧠
And discover how we identified new compounds that might be key for neuroprotection.
🔬 🫐
#Neuroscience#Aging#Biotech (1/5)
It's finally out!
Read our updated story about stochasticity and #aging clocks.
We restructured the paper, reworked the text, and included more validation. 👇 #bioinformatics
We updated our preprint and validated the stochastic clock on ~17k new samples, showing that also a variety of mammalian species, age acceleration (smoking) and deceleration (e.g. calorie-restriction), as well as reprogramming are predictable with just one biological sample+noise
Congratulations to @ArBujarrabal receiving the Stefan-Jentsch-Award at the 6th German-French DNA Repair meeting 2023 in Mainz by Julian Stingele of the German Society for DNA Repair. @imbmainz @CECAD_ @UKKoeln @FOR5504 @UniCologne
Today I presented my thesis work about the DREAM complex at the 6th German-French meeting in #DNArepair and received the DGDR Stefan Jentsch award!! 🎉 A huge honour and a great conference!!
Congratulations @SiyaoWang1005 on the new group leader positions @imbmainz Looking forward to your next breakthrough discoveries on epigenetic regulation of genome stability, inheritance and aging.
📢Announcing the 2nd batch of speakers for the 3rd VitaDAO DeSci & Longevity Symposium!
🗣️Speakers: @Vinz_Sorrentino, Aldo de Pape, @ArBujarrabal, @EmmaTeeling1, @manveerbasra_
Sign up now!👇
https://t.co/bExISgF4zy
@CeronLab@schumacherbj Thank you very much! You are right with the issues of inhibiting DREAM, and although the lin-52 mutant we used is already better than other mutants of DREAM on this, finding a way of isolating DNA repair from the equation is a must! Hopefully we can follow it up :)
It is officially out! It has been a long time. Check the paper on how the DREAM complex represses DNA repair, and limiting its function can keep the genome healthy and without damage!
👇
Our DREAM paper is out: We found the first master regulator of DNA repair capacities! Read and re-tweet now: The DREAM complex functions as conserved master regulator of somatic DNA repair capacities, @CECAD_@UKKoeln@UniCologne
https://t.co/rVMe4rAxaf
@TWBredy @OdedRechavi@schumacherbj Yes, in these non-replicative cells the repair they have is enough to extend beyond the reproductive lifespan and most healthspan. Having even better repair would probably just have been a waste of energy evolutionary speaking. Only now with current lifespans it is an issue.
@PetrovADmitri@OdedRechavi@schumacherbj Yes to the developing! But do not take anything yet. DREAM complex members are involved in other complexes to be wary of and inhibiting DREAM could promote cell division by itself in some cells. More research needs to be done!
@TWBredy @OdedRechavi@schumacherbj Good difficult question. 1st possibility, DNA repair mechanisms might have evolved to be co-regulated with germline+cell cycle genes, so, deregulation of repair genes might hamper differentiated somatic cell function.
@AlexanderMWolf7@schumacherbj@CECAD_@UKKoeln@UniCologne Focusing only on DNA repair, as many somatic cells are replaceable it might be more energy and function efficient to replace a cell as it gets damaged rather than keeping it spending resources on its repair. Just a possibility
@AlexanderMWolf7@schumacherbj@CECAD_@UKKoeln@UniCologne DREAM regulates other things part of the same package; DNA repair+cell division and germline related genes. The effects on somatic cells are good in terms of DNA repair but could be detrimental in other cases. Hopefully we can limit this effect to DNA repair even more, we'll see!
@DavidBahry@schumacherbj We have not looked into this but literature shows that there might be a connection. In the end, DREAM, mTOR, GH, all can regulate initiation of cell cycle, something to dig into!