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Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins

Neurodevelopmental disorders are classified as diseases that cause abnormal functions of the brain or central nervous system. Children with neurodevelopmental disorders show impaired language and speech abilities, learning and memory damage, and poor motor skills. However, we still know very little...

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Autores principales: Li, Junlin, Zhao, Guifang, Gao, Xiaocai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585942/
https://www.ncbi.nlm.nih.gov/pubmed/23425632
http://dx.doi.org/10.1186/1866-1955-5-4
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author Li, Junlin
Zhao, Guifang
Gao, Xiaocai
author_facet Li, Junlin
Zhao, Guifang
Gao, Xiaocai
author_sort Li, Junlin
collection PubMed
description Neurodevelopmental disorders are classified as diseases that cause abnormal functions of the brain or central nervous system. Children with neurodevelopmental disorders show impaired language and speech abilities, learning and memory damage, and poor motor skills. However, we still know very little about the molecular etiology of these disorders. Recent evidence implicates the bromodomain-containing proteins (BCPs) in the initiation and development of neurodevelopmental disorders. BCPs have a particular domain, the bromodomain (Brd), which was originally identified as specifically binding acetyl-lysine residues at the N-terminus of histone proteins in vitro and in vivo. Other domains of BCPs are responsible for binding partner proteins to form regulatory complexes. Once these complexes are assembled, BCPs alter chromosomal states and regulate gene expression. Some BCP complexes bind nucleosomes, are involved in basal transcription regulation, and influence the transcription of many genes. However, most BCPs are involved in targeting. For example, some BCPs function as a recruitment platform or scaffold through their Brds-binding targeting sites. Others are recruited to form a complex to bind the targeting sites of their partners. The regulation mediated by these proteins is especially critical during normal and abnormal development. Mutant BCPs or dysfunctional BCP-containing complexes are implicated in the initiation and development of neurodevelopmental disorders. However, the pathogenic molecular mechanisms are not fully understood. In this review, we focus on the roles of regulatory BCPs associated with neurodevelopmental disorders, including mental retardation, Fragile X syndrome (FRX), Williams syndrome (WS), Rett syndrome and Rubinstein-Taybi syndrome (RTS). A better understanding of the molecular pathogenesis, based upon the roles of BCPs, will lead to screening of targets for the treatment of neurodevelopmental disorders.
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spelling pubmed-35859422013-03-03 Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins Li, Junlin Zhao, Guifang Gao, Xiaocai J Neurodev Disord Review Neurodevelopmental disorders are classified as diseases that cause abnormal functions of the brain or central nervous system. Children with neurodevelopmental disorders show impaired language and speech abilities, learning and memory damage, and poor motor skills. However, we still know very little about the molecular etiology of these disorders. Recent evidence implicates the bromodomain-containing proteins (BCPs) in the initiation and development of neurodevelopmental disorders. BCPs have a particular domain, the bromodomain (Brd), which was originally identified as specifically binding acetyl-lysine residues at the N-terminus of histone proteins in vitro and in vivo. Other domains of BCPs are responsible for binding partner proteins to form regulatory complexes. Once these complexes are assembled, BCPs alter chromosomal states and regulate gene expression. Some BCP complexes bind nucleosomes, are involved in basal transcription regulation, and influence the transcription of many genes. However, most BCPs are involved in targeting. For example, some BCPs function as a recruitment platform or scaffold through their Brds-binding targeting sites. Others are recruited to form a complex to bind the targeting sites of their partners. The regulation mediated by these proteins is especially critical during normal and abnormal development. Mutant BCPs or dysfunctional BCP-containing complexes are implicated in the initiation and development of neurodevelopmental disorders. However, the pathogenic molecular mechanisms are not fully understood. In this review, we focus on the roles of regulatory BCPs associated with neurodevelopmental disorders, including mental retardation, Fragile X syndrome (FRX), Williams syndrome (WS), Rett syndrome and Rubinstein-Taybi syndrome (RTS). A better understanding of the molecular pathogenesis, based upon the roles of BCPs, will lead to screening of targets for the treatment of neurodevelopmental disorders. BioMed Central 2013 2013-02-20 /pmc/articles/PMC3585942/ /pubmed/23425632 http://dx.doi.org/10.1186/1866-1955-5-4 Text en Copyright ©2013 Li et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Li, Junlin
Zhao, Guifang
Gao, Xiaocai
Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins
title Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins
title_full Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins
title_fullStr Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins
title_full_unstemmed Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins
title_short Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins
title_sort development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585942/
https://www.ncbi.nlm.nih.gov/pubmed/23425632
http://dx.doi.org/10.1186/1866-1955-5-4
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