The human methyltransferase MLL4 plays a critical role in embryogenesis and development, and aberrant activity of MLL4 is linked to neurodegenerative and developmental disorders and cancer. MLL4 contains the catalytic SET domain that catalyzes mono methylation of lysine 4 of histone H3 (H3K4me1) and seven plant homeodomain (PHD) fingers, six of which have not been structurally and functionally characterized. Here, we demonstrate that the triple PHD finger cassette of MLL4, harboring its fourth, fifth and sixth PHD fingers (MLL4) forms an integrated module, maintains the binding selectivity of the PHD6 finger toward acetylated lysine 16 of histone H4 (H4K16ac), and is capable of binding to DNA. Our findings highlight functional correlation between H4K16ac and H3K4me1, two major histone modifications that are recognized and written, respectively, by MLL4.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10799173PMC
http://dx.doi.org/10.1016/j.jmb.2023.168212DOI Listing

Publication Analysis

Top Keywords

histone h4k16ac
8
triple phd
8
phd finger
8
finger cassette
8
cassette mll4
8
lysine histone
8
phd fingers
8
mll4
7
histone
4
h4k16ac binding
4

Similar Publications

A noncanonical role of roX RNAs in autosomal epigenetic repression.

Nat Commun

January 2025

Shenzhen Key Laboratory of Synthetic Genomics, Guangdong Provincial Key Laboratory of Synthetic Genomics, Key Laboratory of Quantitative Synthetic Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.

Article Synopsis
  • roX RNAs are essential for male development in Drosophila, and their absence leads to male lethality during late larval stages.
  • They are known for their role in balancing X-linked gene expression but have shown to also target autosomal genes, which had not been extensively studied before.
  • The research highlights that roX RNAs function as both activators of X-linked genes and repressors of autosomal genes through their interactions with specific protein complexes, revealing a complex role in gene regulation.
View Article and Find Full Text PDF

PX-12 modulates vorinostat-induced acetylation and methylation marks in CAL 27 cells.

Epigenomics

December 2024

Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.

Aim: The hypoxic tumor microenvironment (TME) in oral squamous cell carcinoma (OSCC) is primarily regulated by hypoxia-inducible factor-1 alpha (HIF-1α), impacting histone acetylation and methylation, which contribute to drug resistance. Vorinostat, a histone deacetylase inhibitor (HDACi), de-stabilizes HIF-1α, while PX-12, a thioredoxin-1 (Trx-1) inhibitor, prevents HIF-1α accumulation. Combining HDACi with a Trx-1 inhibitor may enhance efficacy and reduce resistance by increasing reactive oxygen species (ROS) in cancer cells.

View Article and Find Full Text PDF

is an old long noncoding RNA recruited for X chromosome dosage compensation in a reptile.

Science

September 2024

Centro de Ciencias Genómicas, Universidad Nacional Autónoma de México (UNAM), CP62210 Cuernavaca, México.

Long noncoding RNAs (lncRNAs) are essential regulatory elements of sex chromosomes that act to equalize gene expression levels between males and females. , , and regulate X chromosomes in placental mammals, marsupials, and , respectively. Because the green anole () shows complete dosage compensation of its X chromosome, we tested whether a lncRNA was involved.

View Article and Find Full Text PDF

Background: As the leading cause of end-stage liver disease, nonalcoholic fatty liver disease (NAFLD) is mainly induced by lipid dyshomeostasis. The translation of endogenous circular RNAs (circRNAs) is closely related to the progression of various diseases, but the involvement of circRNAs in NAFLD has not been determined.

Methods: Combined high-throughput circRNA profiles were used to identify circRNAs with translational potential.

View Article and Find Full Text PDF
Article Synopsis
  • - The study highlights that abnormal trophoblast self-renewal and differentiation in early pregnancy can lead to miscarriages, with the KAT8 enzyme playing a critical role in regulating these processes.
  • - Researchers found that deleting KAT8 in trophoblasts causes severe developmental issues, but boosting the expression of a key marker (CDX2) can partially counteract these defects.
  • - Changes in the levels of KAT8, CDX2, and H4K16ac are linked to recurrent pregnancy loss, suggesting that targeting the KAT8-H4K16ac-CDX2 pathway might be a potential treatment option for this issue.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!