Yicheng Long
@yichenglong.bsky.social
91 followers 180 following 10 posts
Assistant Professor of Biochemistry, Weill Cornell Medicine. www.longlab.org. Studying epigenetics, nucleic acids, stem cells and heart. Cech lab alumnus
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yichenglong.bsky.social
The project is spearheaded by our wonderful research associate Christian Much along with a dream team - grad student Sandy Rajkumar, postdoc Liming Chen, technician John Cohen and our amazing collaborator Dr. Geoff Pitt @geoffrey-pitt.bsky.social & Aravind Gade in his lab @weillcornell.bsky.social.
yichenglong.bsky.social
We also dived into the three mutually exclusive PRC2.1 complexes. Surprisingly, PHF19 antagonizes the role of MTF2 on regulating PRC2 occupancy and H3K27me3 deposition. MTF2 loss-of-function mutants also phenocopies the cardiomyocyte differentiation phenotype of the loss of PRC2.1 line.
yichenglong.bsky.social
PRC2.1 and PRC2.2 exhibits opposing function in cardiomyocyte differentiation, potentially through their specificity on key transcription factor and ion channel genes. Interestingly, loss of PRC2.1 accelerates differentiation and increases spontaneous action potential frequency.
yichenglong.bsky.social
Loss of PRC2.1 or PRC2.2 in hPSCs by separation-of-function mutants led to loss of H3K27me3 in a gene-specific manner. For example, the H3K27me3 peaks at BARHL1 and ARV1 are specifically deposited by PRC2.1 and PRC2.2, respectively. This specificity is observed genome wide.
yichenglong.bsky.social
Excited to share our work on the specificity of PRC2 subcomplexes in stem cell and differentiation. We show that PRC2.1 and PRC2.2 exhibit distinct H3K27 methylation specificity in human pluripotent stem cells and opposing role in differentiation. Now online at Mol Cell: www.cell.com/molecular-ce...
Distinct specificity and functions of PRC2 subcomplexes in human stem cells and cardiac differentiation
Much et al. reveal that the PRC2 subcomplexes PRC2.1 and PRC2.2 play distinct roles in the epigenetic repression of developmental genes in human stem cells. Interactions between the PRC2 core and its ...
www.cell.com
Reposted by Yicheng Long
peterlewislab.bsky.social
We are excited to share our new preprint demonstrating that nucleic acid interactions with SUZ12 constrain PRC2 activity, establishing a kinetic buffer essential for targeted gene silencing and revealing vulnerabilities in diffuse midline gliomas.
www.biorxiv.org/content/10.1...
yichenglong.bsky.social
It provides compelling evidence that the PRC2 subcomplexes act non-redundantly and regulate lineage-specific gene expression through distinct macromolecular interactions. Thanks to our collaborator and neighbor Dr. Geoff Pitt @geoffrey-pitt.bsky.social !
yichenglong.bsky.social
We use a human pluripotent stem cell model and a serial of CRISPR-mediated separation‐of‐function mutants to reveal that distinct Polycomb Repressive Complex 2 (PRC2) subcomplexes (PRC2.1 and PRC2.2) differentially deposit H3K27me3 and oppositely affect cardiomyocyte differentiation.
yichenglong.bsky.social
Thanks for the recognition and kind words, Matthias!