Literature DB >> 26990528

Histone turnover and chromatin accessibility: Critical mediators of neurological development, plasticity, and disease.

Wendy Wenderski1, Ian Maze2,3.   

Abstract

In postmitotic neurons, nucleosomal turnover was long considered to be a static process that is inconsequential to transcription. However, our recent studies in human and rodent brain indicate that replication-independent (RI) nucleosomal turnover, which requires the histone variant H3.3, is dynamic throughout life and is necessary for activity-dependent gene expression, synaptic connectivity, and cognition. H3.3 turnover also facilitates cellular lineage specification and plays a role in suppressing the expression of heterochromatic repetitive elements, including mutagenic transposable sequences, in mouse embryonic stem cells. In this essay, we review mechanisms and functions for RI nucleosomal turnover in brain and present the hypothesis that defects in histone dynamics may represent a common mechanism underlying neurological aging and disease.
© 2016 WILEY Periodicals, Inc.

Entities:  

Keywords:  H3.3; aging; histone variant; neurological disease; nucleosomal turnover; replication-independent

Mesh:

Substances:

Year:  2016        PMID: 26990528      PMCID: PMC4968875          DOI: 10.1002/bies.201500171

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  114 in total

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2.  The atomic structure of the nucleosome core particle.

Authors:  K Luger; A Mäder; D F Sargent; T J Richmond
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3.  Genome-scale profiling of histone H3.3 replacement patterns.

Authors:  Yoshiko Mito; Jorja G Henikoff; Steven Henikoff
Journal:  Nat Genet       Date:  2005-09-11       Impact factor: 38.330

4.  Regulation of nucleosome landscape and transcription factor targeting at tissue-specific enhancers by BRG1.

Authors:  Gangqing Hu; Dustin E Schones; Kairong Cui; River Ybarra; Daniel Northrup; Qingsong Tang; Luca Gattinoni; Nicholas P Restifo; Suming Huang; Keji Zhao
Journal:  Genome Res       Date:  2011-07-27       Impact factor: 9.043

5.  Nucleosomes are context-specific, H2A.Z-modulated barriers to RNA polymerase.

Authors:  Christopher M Weber; Srinivas Ramachandran; Steven Henikoff
Journal:  Mol Cell       Date:  2014-03-06       Impact factor: 17.970

6.  Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.

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7.  Histone H2A.Z subunit exchange controls consolidation of recent and remote memory.

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Review 8.  Role of nucleosome remodeling in neurodevelopmental and intellectual disability disorders.

Authors:  Alberto J López; Marcelo A Wood
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Authors:  Simon J Elsässer; Laura A Banaszynski; Kyung-Min Noh; Nichole Diaz; C David Allis
Journal:  Nature       Date:  2015-05-04       Impact factor: 49.962

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  10 in total

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Review 5.  Chromatin Changes Associated with Neuronal Maintenance and Their Pharmacological Application.

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Review 9.  Endogenous Retroviruses (ERVs): Does RLR (RIG-I-Like Receptors)-MAVS Pathway Directly Control Senescence and Aging as a Consequence of ERV De-Repression?

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