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New UNC Charlotte study reveals how just three molecules can launch gene-silencing condensates, organizing the epigenome and controlling stem cell differentiation

A new study by UNC Charlotte scientists has discovered a self-clustering mechanism in the Polycomb protein CBX2 that is essential for initiating gene-repressive condensates and guiding stem cells toward their proper fates. The researchers found that CBX2 clusters recruit two Polycomb repressive complexes, creating multicomponent repres...

SourceUniversity of North Carolina at Charlotte·JournalMolecular Cell·TypeExperimental study·DateMar 4, 2026

DGIST has successfully discovered a novel DNA damage repair pathway in human cells

A team of scientists has identified a novel DNA damage repair pathway in human cells, revealing that proteins present in the nuclear membrane directly interact with damaged DNA. This breakthrough could lead to the development of new cancer treatments that target this pathway and overcome treatment resistance.

SourceDGIST (Daegu Gyeongbuk Institute of Science and Technology)·JournalProceedings of the National Academy of Sciences·DateAug 14, 2025

Temperature steers plant cell fate through epigenetic reprogramming

Researchers discovered temperature influences plant cell fate by regulating epigenetic marks. Low ambient temperatures can rescue developmental defects by compensating for PRC2 loss, highlighting the importance of H3K27me3 in maintaining cellular identity.

SourceChinese Academy of Sciences Headquarters·JournalDevelopmental Cell·TypeExperimental study·DateApr 27, 2025

Discovering cancers of epigenetic origin without DNA mutation

Researchers have found that genetic mutations are not essential for cancer onset, and instead, epigenetic dysregulation plays a crucial role. Epigenetic changes can cause gene expression to be altered, leading to tumour formation even after the signal has been restored.

SourceCNRS·JournalNature·DateApr 24, 2024

USC Stem Cell study throws our understanding of gene regulation for a loop

Researchers discovered that PDS5A modifies DNA loops without affecting histone modifications, enabling the study of loop-mediated gene silencing. The loss of PDS5A disrupted genome organization, leading to aberrant gene activation and potentially driving diseases like cancer and developmental disorders.

SourceKeck School of Medicine of USC·JournalNature Communications·TypeExperimental study·DateJan 16, 2024
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“We were dancing around the lab” – cellular identity discovery has potential to impact cancer treatments

Researchers at Trinity College Dublin have discovered a new process that explains why cells have unique identities. By studying Polycomb protein complexes, the team found that different forms of these proteins recruit distinct complexes to DNA, shedding light on cellular identity and its potential impact on cancer treatments.

SourceTrinity College Dublin·JournalMolecular Cell·DateApr 7, 2023

Oncotarget | Unveiling the non-canonical functions of EZH2 in prostate cancer

Researchers from Northwestern University discuss the multifaceted tumorigenic functions of EZH2, including its role in regulating translation and coactivating transcription. This new understanding may provide novel insights into advancing EZH2-targeting strategies for prostate cancer patients.

SourceImpact Journals LLC·JournalOncotarget·TypeCommentary/editorial·DateMar 3, 2023

Study reveals how the ovarian reserve is established

Researchers identify PRC1 as key to establishing and maintaining ovarian reserve, providing insights into female reproductive health and lifespan. The study's findings may help explain premature ovarian failure and infertility in humans.

SourceUniversity of California - Davis·JournalNature Communications·TypeExperimental study·DateAug 10, 2022
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Epigenetic switch helps keep early embryo cells on the right track

A study reveals an epigenetic switch that restricts early embryo cells from differentiating into certain tissue lineages. The research identifies PRC2 as a key regulator of gene expression in embryonic development, allowing for better control of stem cell specialization and blastoid formation.

SourceKU Leuven·JournalNature Cell Biology·TypeExperimental study·DateJun 13, 2022

A novel neurological disorder associated with the Polycomb complex identified

Researchers discovered a novel neurological disorder caused by spontaneous mutations in the RNF2 gene, leading to symptoms such as intellectual disabilities, seizures, and feeding difficulties. The study, led by Dr. Shinya Yamamoto and Dr. Vandana Shashi, found that loss-of-function variants in RNF2 disrupt normal neuronal development ...

SourceTexas Children's Hospital·JournalHuman Molecular Genetics·DateJul 8, 2021

Mount Sinai researchers identify mechanisms that are essential for proper skin development

Researchers found that Polycomb repressive complex 1 (PRC1) and Polycomb repressive complex 2 (PRC2) maintain the skin-specific gene expression pattern necessary for proper development of the skin. The study suggests that targeting both complexes may be a more effective form of treatment for certain cancers.

SourceThe Mount Sinai Hospital / Mount Sinai School of Medicine·JournalGenes & Development·DateFeb 18, 2021

'BAH-code' reader senses gene-silencing tag in cells

Researchers have identified a new and evolutionarily conserved pathway responsible for silencing genes in mammalian cells. BAHCC1 protein is involved in the Polycomb pathway, which generates a chemical tag to silence genes, and its high expression is linked to leukemia, challenging current understanding of gene silencing.

SourceUNC Lineberger Comprehensive Cancer Center·JournalNature Genetics·DateNov 2, 2020
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New discovery explains why cells with identical genes perform unique jobs

A team from Trinity College Dublin discovered two new families of proteins, PALI1 and PALI2, that are vital for embryonic development and controlling cellular identity in complex animals. These proteins help understand why cells look and act differently despite having identical genes.

SourceTrinity College Dublin·JournalMolecular Cell·DateApr 5, 2018
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Penn biologists show how plants turn off genes they don't need

Researchers at the University of Pennsylvania have discovered a mechanism for regulating gene activity in plants by identifying small DNA sequences called Polycomb response elements (PREs) that direct the silencing of genes. These PREs can be manipulated using gene-editing techniques to alter gene expression without adding foreign gene...

SourceUniversity of Pennsylvania·JournalNature Genetics·DateAug 21, 2017

Jarid2 may break the Polycomb silence

Researchers found that Jarid2, a component of the Polycomb repressive complex 2, occasionally activates gene expression in fruit fly embryos. This challenges the traditional view of Polycomb proteins as transcriptional repressors, suggesting a more complex role for PRC2 and its components in development and cancer.

SourceStowers Institute for Medical Research·JournalMolecular and Cellular Biology·DateApr 30, 2012

How the wrong genes are repressed: New finding from UCL

Researchers at University College London have identified a new mechanism for how polycomb proteins repress the wrong genes in embryonic stem cells. The discovery has significant implications for tissue engineering and cell differentiation, as it reveals how polycomb proteins control gene activity through interaction with short RNAs.

SourceUniversity College London·JournalMolecular Cell·DateJun 11, 2010

Tags on, tags off

Researchers at EMBL identified a new Polycomb group complex, PR-DUB, which surprisingly removes the same gene-silencing tag as another complex. This unexpected behavior may be a case of fine-tuning to maintain optimal levels of chemical tagging.

SourceEuropean Molecular Biology Laboratory·JournalNature·DateMay 3, 2010
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Sugarcoating fruit fly development

Researchers found that adding a sugar tag to nuclear proteins is vital for normal development in fruit flies, revealing a critical link between Ogt and Polycomb protein function.

SourceEuropean Molecular Biology Laboratory·JournalScience·DateMay 29, 2009

Mapping the foundation of human development

Researchers successfully mapped the regulatory circuitry of human embryonic stem cells using microarray technology. The study reveals that Polycomb group proteins play a crucial role in repressing genes essential for later development, leading to uncontrolled growth when these genes are lost.

SourceWhitehead Institute for Biomedical Research·JournalCell·DateApr 20, 2006

How embryonic stem cells maintain their identity

Researchers found that Polycomb proteins repress developmental genes, while bivalent domains mark key genes with both repressive and activating characteristics. This helps explain embryonic stem cell stability and differentiation potential.

SourceCell Press·JournalCell·DateApr 20, 2006
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Mapping dynamic Polycomb group proteins during Drosophila development

Researchers mapped dynamic Polycomb group protein PC and PH across various developmental stages in Drosophila. The study reveals the proteins' diverse binding locations, implying different gene silencing mechanisms. Further analysis is needed to understand their role in development and conservation across species.

SourcePLOS·JournalPLOS Biology·DateApr 19, 2006

Study helps explain gene silencing in the developing embryo

Researchers have linked Polycomb gene silencing to histone protein methylation, explaining the permanence of Hox gene silencing. The study found that Polycomb proteins function through methylating a specific lysine residue on histone 3, leading to permanent gene silencing.

SourceUniversity of North Carolina Health Care·JournalScience·DateOct 29, 2002