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Cerebellar organoids model cell type-specific FOXP2 expression during human cerebellar development
by
Apsley, Elizabeth J
, Cowley, Sally A
, Becker, Esther B E
, Riepsaame, Joey
in
Cerebellum
/ CRISPR
/ Forkhead protein
/ Foxp2 protein
/ Inhibitory postsynaptic potentials
/ Neurodevelopmental disorders
/ Neuroscience
/ Organoids
/ Population studies
/ Purkinje cells
/ Transcriptomics
2024
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Cerebellar organoids model cell type-specific FOXP2 expression during human cerebellar development
by
Apsley, Elizabeth J
, Cowley, Sally A
, Becker, Esther B E
, Riepsaame, Joey
in
Cerebellum
/ CRISPR
/ Forkhead protein
/ Foxp2 protein
/ Inhibitory postsynaptic potentials
/ Neurodevelopmental disorders
/ Neuroscience
/ Organoids
/ Population studies
/ Purkinje cells
/ Transcriptomics
2024
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Do you wish to request the book?
Cerebellar organoids model cell type-specific FOXP2 expression during human cerebellar development
by
Apsley, Elizabeth J
, Cowley, Sally A
, Becker, Esther B E
, Riepsaame, Joey
in
Cerebellum
/ CRISPR
/ Forkhead protein
/ Foxp2 protein
/ Inhibitory postsynaptic potentials
/ Neurodevelopmental disorders
/ Neuroscience
/ Organoids
/ Population studies
/ Purkinje cells
/ Transcriptomics
2024
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Cerebellar organoids model cell type-specific FOXP2 expression during human cerebellar development
Paper
Cerebellar organoids model cell type-specific FOXP2 expression during human cerebellar development
2024
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Overview
In this study, we demonstrate the potential of cerebellar organoids for studying features of early human cerebellar development. Forkhead box protein P2 (FOXP2) is a transcription factor associated with speech and language development that is highly expressed in the developing brain. However, little attention has been directed to the study of FOXP2 in the early developing cerebellum. We used CRISPR gene editing in human iPSCs to generate a fluorescent FOXP2-reporter line. By combining transcriptomic analysis of iPSC-derived cerebellar organoids with published cerebellar datasets, we describe the expression and identify potential downstream targets of FOXP2 in the early developing human cerebellum. Our results highlight expression of FOXP2 in early human Purkinje cells and cerebellar nuclei neurons, and the vulnerability of these cell populations to neurodevelopmental disorders. Our study demonstrates the power of cerebellar organoids to model early human developmental processes and disorders.Competing Interest StatementThe authors have declared no competing interest.
Publisher
Cold Spring Harbor Laboratory Press,Cold Spring Harbor Laboratory
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