The emerging roles for the chromatin structure regulators CTCF and cohesin in neurodevelopment and behavior

Liron Davis, Itay Onn, Evan Elliott

Research output: Contribution to journalReview articlepeer-review

22 Scopus citations

Abstract

Recent genetic and technological advances have determined a role for chromatin structure in neurodevelopment. In particular, compounding evidence has established roles for CTCF and cohesin, two elements that are central in the establishment of chromatin structure, in proper neurodevelopment and in regulation of behavior. Genetic aberrations in CTCF, and in subunits of the cohesin complex, have been associated with neurodevelopmental disorders in human genetic studies, and subsequent animal studies have established definitive, although sometime opposing roles, for these factors in neurodevelopment and behavior. Considering the centrality of these factors in cellular processes in general, the mechanisms through which dysregulation of CTCF and cohesin leads specifically to neurological phenotypes is intriguing, although poorly understood. The connection between CTCF, cohesin, chromatin structure, and behavior is likely to be one of the next frontiers in our understanding of the development of behavior in general, and neurodevelopmental disorders in particular.

Original languageEnglish
Pages (from-to)1205-1214
Number of pages10
JournalCellular and Molecular Life Sciences
Volume75
Issue number7
DOIs
StatePublished - 1 Apr 2018

Bibliographical note

Publisher Copyright:
© 2017, Springer International Publishing AG, part of Springer Nature.

Funding

We would like to thank Anita Impagliazzo for providing professional graphical support in preparing the figure for this manuscript. This study has been supported by Israel Science Foundation Grant 1099/16 (I.O) and Israel Science Foundation Grant 898/17 (E.E).

FundersFunder number
Israel Science Foundation1099/16, 898/17

    Keywords

    • Behavior
    • CTCF
    • Chromatin structure
    • Cohesin
    • Condensin
    • Intellectual disability
    • Neurodevelopment
    • SMC

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