نتایج جستجو برای: histone3 trimethylation

تعداد نتایج: 1508  

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2010
Swati Gupta Se Y Kim Sonja Artis David L Molfese Armin Schumacher J David Sweatt Richard E Paylor Farah D Lubin

It has been established that regulation of chromatin structure through post-translational modification of histone proteins, primarily histone H3 phosphorylation and acetylation, is an important early step in the induction of synaptic plasticity and formation of long-term memory. In this study, we investigated the contribution of another histone modification, histone methylation, to memory forma...

Journal: :The EMBO journal 2011
M Behfar Ardehali Amanda Mei Katie L Zobeck Matthieu Caron John T Lis Thomas Kusch

Histone H3 lysine 4 trimethylation (H3K4me3) is a major hallmark of promoter-proximal histones at transcribed genes. Here, we report that a previously uncharacterized Drosophila H3K4 methyltransferase, dSet1, and not the other putative histone H3K4 methyltransferases (Trithorax; Trithorax-related protein), is predominantly responsible for histone H3K4 trimethylation. Functional and proteomics s...

Journal: :The Journal of Cell Biology 2007
Alexandre Blais Chris J.C. van Oevelen Raphaël Margueron Diego Acosta-Alvear Brian David Dynlacht

The retinoblastoma tumor suppressor protein (pRb) is involved in mitotic exit, promoting the arrest of myoblasts, and myogenic differentiation. However, it is unclear how permanent cell cycle exit is maintained in differentiated muscle. Using RNA interference, expression profiling, and chromatin immunoprecipitations, we show that pRb is essential for cell cycle exit and the differentiation of m...

Journal: :Genes & development 2015
Constance Alabert Teresa K Barth Nazaret Reverón-Gómez Simone Sidoli Andreas Schmidt Ole N Jensen Axel Imhof Anja Groth

Epigenetic states defined by chromatin can be maintained through mitotic cell division. However, it remains unknown how histone-based information is transmitted. Here we combine nascent chromatin capture (NCC) and triple-SILAC (stable isotope labeling with amino acids in cell culture) labeling to track histone modifications and histone variants during DNA replication and across the cell cycle. ...

Journal: :Developmental cell 2013
Phillip Grote Lars Wittler David Hendrix Frederic Koch Sandra Währisch Arica Beisaw Karol Macura Gaby Bläss Manolis Kellis Martin Werber Bernhard G Herrmann

The histone-modifying complexes PRC2 and TrxG/MLL play pivotal roles in determining the activation state of genes controlling pluripotency, lineage commitment, and cell differentiation. Long noncoding RNAs (lncRNAs) can bind to either complex, and some have been shown to act as modulators of PRC2 or TrxG/MLL activity. Here we show that the lateral mesoderm-specific lncRNA Fendrr is essential fo...

Journal: :Molecular and Cellular Biology 2010

Journal: :Neuro-oncology 2022

Abstract Malignant peripheral nerve sheath tumors (MPNSTs) are the most common cause of death in patients with neurofibromatosis type 1 (NF-1) yet non-invasive diagnosis and risk stratification NF-1-associated remains challenging. Moreover, relationship between radiographic features pathologic measures such as mitotic index necrosis, or molecular markers malignant transformation H3K27 trimethyl...

Journal: :Blood 2011
Luca Mazzarella Helle F Jørgensen Jorge Soza-Ried Anna V Terry Stella Pearson Georges Lacaud Valerie Kouskoff Matthias Merkenschlager Amanda G Fisher

Many lineage-specific developmental regulator genes are transcriptionally primed in embryonic stem (ES) cells; RNA Pol(II) is bound at their promoters but is prevented from productive elongation by the activity of polycomb repressive complexes (PRC) 1 and 2. This epigenetically poised state is thought to enable ES cells to rapidly execute multiple differentiation programs and is recognized by a...

Journal: :Molecular and cellular biology 2012
Barry M Zee Laura-Mae P Britton Daniel Wolle Devorah M Haberman Benjamin A Garcia

The connections between various nuclear processes and specific histone posttranslational modifications are dependent to a large extent on the acquisition of those modifications after histone synthesis. The reestablishment of histone posttranslational modifications after S phase is especially critical for H3K9 and H3K27 trimethylation, both of which are linked with epigenetic memory and must be ...

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