نتایج جستجو برای: mef2 و hdac4

تعداد نتایج: 761841  

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1995
G E Lyons B K Micales J Schwarz J F Martin E N Olson

Members of the myocyte enhancer factor 2 (MEF2) gene family are expressed in a dynamic pattern during development of the CNS of pre- and postnatal mice. The four MEF2 genes, Mef2A, -B, -C, -D, encode transcription factors belonging to the MADS (MCM1-agamous-deficiens-serum response factor) superfamily of DNA binding proteins. MEF2 factors have previously been shown to be positive regulators of ...

Journal: :Neuron 2013
Anna Sivachenko Yue Li Katharine C. Abruzzi Michael Rosbash

The transcription factor Mef2 regulates activity-dependent neuronal plasticity and morphology in mammals, and clock neurons are reported to experience activity-dependent circadian remodeling in Drosophila. We show here that Mef2 is required for this daily fasciculation-defasciculation cycle. Moreover, the master circadian transcription complex CLK/CYC directly regulates Mef2 transcription. ChIP...

Journal: :Molecular and cellular biology 1996
J D Molkentin A B Firulli B L Black J F Martin C M Hustad N Copeland N Jenkins G Lyons E N Olson

There are four members of the myocyte enhancer binding factor 2 (MEF2) family of transcription factors, MEF2A, -B, -C, and -D, that have homology within an amino-terminal MADS box and an adjacent MEF2 domain that together mediate dimerization and DNA binding. MEF2A, -C, and -D have previously been shown to bind an A/T-rich DNA sequence in the control regions of numerous muscle-specific genes, w...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2013
Bradford M Elmer Myka L Estes Stephanie L Barrow A Kimberley McAllister

Major histocompatibility complex class I (MHCI) molecules negatively regulate cortical connections and are implicated in neurodevelopmental disorders, including autism spectrum disorders and schizophrenia. However, the mechanisms that mediate these effects are unknown. Here, we report a novel MHCI signaling pathway that requires the myocyte enhancer factor 2 (MEF2) transcription factors. In you...

2017
Juan J. Arredondo Jorge Vivar Sara Laine-Menéndez Leticia Martínez-Morentin Margarita Cervera

CF2 and Mef2 influence a variety of developmental muscle processes at distinct stages of development. Nevertheless, the exact nature of the CF2-Mef2 relationship and its effects on muscle building remain yet to be resolved. Here, we explored the regulatory role of CF2 in the Drosophila embryo muscle formation. To address this question and not having proper null CF2 mutants we exploited loss or ...

Journal: :Neuron 2008
Steven W. Flavell Tae-Kyung Kim Jesse M. Gray David A. Harmin Martin Hemberg Elizabeth J. Hong Eirene Markenscoff-Papadimitriou Daniel M. Bear Michael E. Greenberg

Although many transcription factors are known to control important aspects of neural development, the genome-wide programs that are directly regulated by these factors are not known. We have characterized the genetic program that is activated by MEF2, a key regulator of activity-dependent synapse development. These MEF2 target genes have diverse functions at synapses, revealing a broad role for...

2011
Wenwu Wu Stefan de Folter Xia Shen Wenqian Zhang Shiheng Tao

BACKGROUND The myocyte enhancer factor 2 (MEF2) gene family is broadly expressed during the development and maintenance of muscle cells. Although a great deal has been elucidated concerning MEF2 transcription factors' regulation of specific gene expression in diverse programs and adaptive responses, little is known about the origin and evolution of the four members of the MEF2 gene family in ve...

Journal: :Molecular biology of the cell 2009
Huibin Tang Peter Macpherson Michael Marvin Eric Meadows William H Klein Xiang-Jiao Yang Daniel Goldman

Muscle activity contributes to formation of the neuromuscular junction and affects muscle metabolism and contractile properties through regulated gene expression. However, the mechanisms coordinating these diverse activity-regulated processes remain poorly characterized. Recently, it was reported that histone deacetylase 4 (HDAC4) can mediate denervation-induced myogenin and nicotinic acetylcho...

2016

1 يوجشناد سانشراک ی ،هیذغت مولع دشرا ،نارهت یکشزپ مولع هاگشناد ،یسانش میژر و هیذغت هدکشناد ناریا 2 لوئسم هدنسیون : هورگ رایداتسا هیذغت هعماج ،ناریا ،نارهت یکشزپ مولع هاگشناد ،یسانش میژر و هیذغت هدکشناد ، یکینورتکلا تسپ : [email protected] 3 داتسا هورگ هیذغت هعماج هدکشناد، هیذغت میژرو هاگشناد،ینامرد مولع یکشزپ ،نارهت ناریا 4 يارتکد تملاس تاقیقحت یلم وتیتسنا ،ناهفصا یتشادهب ت...

2012
Shouji Matsushima Junya Kuroda Tetsuro Ago Peiyong Zhai Ji Yeon Park Lai-Hua Xie Bin Tian Junichi Sadoshima

Subject codes: [15] Hypertrophy [91] Oxidative stress [148] Heart failure basic studies In November 2012, the average time from submission to first decision for all original research papers submitted to Circulation Research was 15.8 days. ABSTRACT Rationale: Oxidation of cysteine residues in class II histone deacetylases (HDACs), including HDAC4, causes nuclear exit, thereby inducing cardiac hy...

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