نتایج جستجو برای: histone demethylases

تعداد نتایج: 43210  

2010
Jillian M. Hagel Peter J. Facchini

Demethylases play a pivitol role in numerous biological processes from covalent histone modification and DNA repair to specialized metabolism in plants and microorganisms. Enzymes that catalyze O- and N-demethylation include 2-oxoglutarate (2OG)/Fe(II)-dependent dioxygenases, cytochromes P450, Rieske-domain proteins and flavin adenine dinucleotide (FAD)-dependent oxidases. Proposed mechanisms f...

Journal: :EMBO reports 2009
Tanya Shaw Paul Martin

Tissue repair is a complex process that requires wound-edge cells to proliferate and migrate, which in turn necessitates induction of a large repair transcriptome. Epigenetic modifications have emerged as crucial regulators of gene expression. Here, we ask whether epigenetic reprogramming might contribute to the concerted induction of repair genes by wound-edge cells. Polycomb group proteins (P...

Journal: :Cell 2016
Carsten Merkwirth Virginija Jovaisaite Jenni Durieux Olli Matilainen Sabine D. Jordan Pedro M. Quiros Kristan K. Steffen Evan G. Williams Laurent Mouchiroud Sarah U. Tronnes Virginia Murillo Suzanne C. Wolff Reuben J. Shaw Johan Auwerx Andrew Dillin

Across eukaryotic species, mild mitochondrial stress can have beneficial effects on the lifespan of organisms. Mitochondrial dysfunction activates an unfolded protein response (UPR(mt)), a stress signaling mechanism designed to ensure mitochondrial homeostasis. Perturbation of mitochondria during larval development in C. elegans not only delays aging but also maintains UPR(mt) signaling, sugges...

2014
Cecilia Mannironi Marco Proietto Francesca Bufalieri Enrico Cundari Angela Alagia Svetlana Danovska Teresa Rinaldi Valeria Famiglini Antonio Coluccia Giuseppe La Regina Romano Silvestri Rodolfo Negri

BACKGROUND Histone demethylases (HDMs) have a prominent role in epigenetic regulation and are emerging as potential therapeutic cancer targets. The search for small molecules able to inhibit HDMs in vivo is very active but at the present few compounds were found to be specific for defined classes of these enzymes. METHODOLOGY/PRINCIPAL FINDINGS In order to discover inhibitors specific for H3K...

Journal: :Cell 2007
Tomek Swigut Joanna Wysocka

Methylation of lysine 27 on histone H3 (H3K27me) by the Polycomb complex (PRC2) proteins is associated with gene silencing in many developmental processes. A cluster of recent papers (Agger et al., 2007; De Santa et al., 2007; Lan et al., 2007; Lee et al., 2007) identify the JmjC-domain proteins UTX and JMJD3 as H3K27-specific demethylases that remove this methyl mark, enabling the activation o...

2013
Richard J Hopkinson Louise J Walport Martin Münzel Nathan R Rose Tristan J Smart Akane Kawamura Timothy D W Claridge Christopher J Schofield

Jobs on the side: Substrate selectivity studies indicate that members of the biomedically important JmjC demethylase family of histone N(ε)-methyllysine demethylases are capable of catalyzing the de-N-alkylation of groups other than N-methyl and can catalyze reactions that form stable hydroxylated products. The differences in binding preferences in this set of enzymes may be helpful in the desi...

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