Functions and interactions of mammalian KDM5 demethylases

E Pavlenko, T Ruengeler, P Engel, S Poepsel - Frontiers in genetics, 2022 - frontiersin.org
Mammalian histone demethylases of the KDM5 family are mediators of gene expression
dynamics during developmental, cellular differentiation, and other nuclear processes. They …

Molecular mechanisms of KDM5A in cellular functions: Facets during development and disease

R Kirtana, S Manna, SK Patra - Experimental Cell Research, 2020 - Elsevier
Gene expression is influenced at many layers by a fine-tuned crosstalk between multiple
extrinsic signalling pathways and intrinsic regulatory molecules that respond to …

Theoretical analysis of Polycomb-Trithorax systems predicts that poised chromatin is bistable and not bivalent

K Sneppen, L Ringrose - Nature communications, 2019 - nature.com
Abstract Polycomb (PcG) and Trithorax (TrxG) group proteins give stable epigenetic memory
of silent and active gene expression states, but also allow poised states in pluripotent cells …

Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity

JS Witteveen, MH Willemsen, TCD Dombroski… - Nature Genetics, 2016 - nature.com
Numerous genes are associated with neurodevelopmental disorders such as intellectual
disability and autism spectrum disorder (ASD), but their dysfunction is often poorly …

Physical and functional interaction between SET1/COMPASS complex component CFP-1 and a Sin3S HDAC complex in C. elegans

F Beurton, P Stempor, M Caron, A Appert… - Nucleic Acids …, 2019 - academic.oup.com
The CFP1 CXXC zinc finger protein targets the SET1/COMPASS complex to non-methylated
CpG rich promoters to implement tri-methylation of histone H3 Lys4 (H3K4me3). Although …

A Drosophila model of intellectual disability caused by mutations in the histone demethylase KDM5

S Zamurrad, HAM Hatch, C Drelon, HM Belalcazar… - Cell reports, 2018 - cell.com
Mutations in KDM5 family histone demethylases cause intellectual disability in humans.
However, the molecular mechanisms linking KDM5-regulated transcription and cognition …

Regulation of Aspergillus nidulans CreA-Mediated Catabolite Repression by the F-Box Proteins Fbx23 and Fbx47

LJ de Assis, M Ulas, LNA Ries, NAM El Ramli… - MBio, 2018 - Am Soc Microbiol
The attachment of one or more ubiquitin molecules by SCF (S kp–C ullin–F-box) complexes
to protein substrates targets them for subsequent degradation by the 26S proteasome …

SIN-3 acts in distinct complexes to regulate the germline transcriptional program in Caenorhabditis elegans

VJ Robert, M Caron, L Gely, A Adrait… - …, 2023 - journals.biologists.com
The transcriptional co-regulator SIN3 influences gene expression through multiple
interactions that include histone deacetylases. Haploinsufficiency and mutations in SIN3 are …

Sin3a regulates epithelial progenitor cell fate during lung development

C Yao, G Carraro, B Konda, X Guan, T Mizuno… - …, 2017 - journals.biologists.com
Mechanisms that regulate tissue-specific progenitors for maintenance and differentiation
during development are poorly understood. Here, we demonstrate that the co-repressor …

A KDM5–Prospero transcriptional axis functions during early neurodevelopment to regulate mushroom body formation

HAM Hatch, HM Belalcazar, OJ Marshall, J Secombe - Elife, 2021 - elifesciences.org
Mutations in the lysine demethylase 5 (KDM5) family of transcriptional regulators are
associated with intellectual disability, yet little is known regarding their spatiotemporal …