Literature DB >> 25195934

The role of BAF (mSWI/SNF) complexes in mammalian neural development.

Esther Y Son, Gerald R Crabtree.   

Abstract

The BAF (mammalian SWI/SNF) complexes are a family of multi-subunit ATP-dependent chromatin remodelers that use ATP hydrolysis to alter chromatin structure. Distinct BAF complex compositions are possible through combinatorial assembly of homologous subunit families and can serve non-redundant functions. In mammalian neural development, developmental stage-specific BAF assemblies are found in embryonic stem cells, neural progenitors and postmitotic neurons. In particular, the neural progenitor-specific BAF complexes are essential for controlling the kinetics and mode of neural progenitor cell division, while neuronal BAF function is necessary for the maturation of postmitotic neuronal phenotypes as well as long-term memory formation. The microRNA-mediated mechanism for transitioning from npBAF to nBAF complexes is instructive for the neuronal fate and can even convert fibroblasts into neurons. The high frequency of BAF subunit mutations in neurological disorders underscores the rate-determining role of BAF complexes in neural development, homeostasis, and plasticity.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  BAF; Coffin-Siris syndrome; Nicolaides-Baraitser syndrome; autism; chromatin remodeling; intellectual disability; mammalian SWI/SNF; microRNA; neural development; schizophrenia

Mesh:

Substances:

Year:  2014        PMID: 25195934      PMCID: PMC4405377          DOI: 10.1002/ajmg.c.31416

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  175 in total

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Journal:  Nat Genet       Date:  2012-02-26       Impact factor: 38.330

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9.  Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy.

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Journal:  Nat Genet       Date:  2013-05-05       Impact factor: 38.330

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  69 in total

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Review 2.  Intermediate progenitors and Tbr2 in cortical development.

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Review 5.  From trans to cis: transcriptional regulatory networks in neocortical development.

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6.  Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.

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Journal:  Am J Hum Genet       Date:  2018-12-20       Impact factor: 11.025

Review 7.  COMPASS and SWI/SNF complexes in development and disease.

Authors:  Bercin K Cenik; Ali Shilatifard
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8.  Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.

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Review 10.  The role of ARID1B, a BAF chromatin remodeling complex subunit, in neural development and behavior.

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Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  2018-08-24       Impact factor: 5.067

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