Hi Sumin! Thanks for your thoughts. Yes, more quantitative, time-resolved data would be exciting.
24.02.2026 03:30
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Hi Sumin! Thanks for your thoughts. Yes, more quantitative, time-resolved data would be exciting.
Nice work! I like the different models proposed. I wonder if the part of the mechanism could involve the Polycomb domain acting as a roadblock to loop extrusion, thereby limiting E-P interactions? I agree that "Degron-based experiments combined with single-cell measurements" will be important.
Great news :) Congrats, Takashi!
😂
- Independent localization of H2AK119Ub and H3K27me3 in worm embryos.
- Removing Ub did not influence K27me3 levels, and vice versa.
- It is interesting that different cells/organisms utilize conserved chromatin-modifying machineries differently.
www.science.org/doi/10.1126/...
I like the stratification, too.
Also, quite striking threshold at AT content ~0.55 (Fig. 2D).
We know how things always take longer than we hope... 😅 I hope you are doing well!
Congrats, Tien-Chi! Quite striking differences in the nuclear organization.
Thanks - I love your inducible, time-resolved experiments in this (and your past) papers!
We did journal club today on this preprint - interesting parallels that CHD4 and its partners block aberrant TF binding in mESCs (this preprint), human cells (PMID:38281186), and fly testis (PMID:28522526).
Fascinated by how CHD4 controls cryptic regulatory elements without a strong presence there.
Exciting work on orphan genes in fertilization and evolution!
Congrats, Anna! 🎉
Avidity.
In plants, PRC2 accessory VEL proteins polymerize much like PRC1 subunits in animals, reinforcing silencing. Multimerization - overcoming weak affinity through 'avidity' - seems to be an important conserved principle in chromatin regulation.
pubmed.ncbi.nlm.nih.gov/40858112/
Donated. FlyBase is a truly essential resource!
Congrats, Ellen! This is so exciting 😊
Thanks for the explanation, Li. It is a good reminder to me not to assume all Aly-class genes regulate the same targets. Looking forward to learn what you find about their roles in de novo genes. Congrats again!
Exciting work!
Many Achi/Vis targets seem not expressed in the tMAC (aly) mutant (as you discussed). Curious if Aly motif (AGYWGGC) sits upstream of Achi/Vis motif in de novo genes. If so, it is interesting how selection resulted in a simple, but still reasonably complex regulatory syntax.
A brief mountain break.
Reducing H1 levels (by CRAMP1 KD) derepresses PRC2 target genes without reducing H3K27me3. It was interesting:
1) once again, H3K27me3 mark alone seems not sufficient for gene repression,
2) how is H1 deposited at Polycomb target sites?
Congrats, Iva!
Beautifully written, Susanna! 😊
True: my ESI MIRA, submitted last February, was withdrawn three weeks before the study section because of a support letter. No sub-award, no expected co-authorship, just a letter. So be careful - their definition of 'collaboration' is very broad.
Congrats, Susanna!! 🎉
Congrats on your exciting work!
I find unstructured regions in proteins enigmatic and very interesting.
Congrats on your exciting work!
Great news! Congratulations!! 🎉
" The common genetic marker Stubble influences Fab2L transgene expression" - balancer and marker mutations are not always inert.
Thank you. I emailed his office.
Today’s the day! I’m happy to announce that the Murphy Lab will be moving to Cornell this July! The lab will be in Biotech and I’ll be joining the Department of Molecular Biology and Genetics. There will be lots of recruiting soon, including students and postdocs. Please RT. 🙏 TY.
Great opportunity for postbacs to do exciting research and gain experience before graduate school!