Unraveling the mysteries of MYT1L: From reprogramming factor to multifaceted regulator of neuronal differentiation
- PMID: 34856129
- DOI: 10.1016/j.neuron.2021.11.006
Unraveling the mysteries of MYT1L: From reprogramming factor to multifaceted regulator of neuronal differentiation
Abstract
In this issue of Neuron, Chen et al. (2021) generated a mouse model for haploinsufficiency of MYT1L. MYT1L is widely used in neuronal reprogramming, and de novo mutations have been linked to a neurodevelopmental syndrome. Extensive characterization in this study better delineates MYT1L's role in transcriptional regulation and neuronal differentiation.
Keywords: Myt1l; autism; gene transcription; intellectual disability; neuronal development.
Copyright © 2021 Elsevier Inc. All rights reserved.
Comment on
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A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturation.Neuron. 2021 Dec 1;109(23):3775-3792.e14. doi: 10.1016/j.neuron.2021.09.009. Epub 2021 Oct 5. Neuron. 2021. PMID: 34614421 Free PMC article.
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