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Developmental cell death of cortical projection neurons is controlled by a Bcl11a/Bcl6-dependent pathway.


ABSTRACT: Developmental neuron death plays a pivotal role in refining organization and wiring during neocortex formation. Aberrant regulation of this process results in neurodevelopmental disorders including impaired learning and memory. Underlying molecular pathways are incompletely determined. Loss of Bcl11a in cortical projection neurons induces pronounced cell death in upper-layer cortical projection neurons during postnatal corticogenesis. We use this genetic model to explore genetic mechanisms by which developmental neuron death is controlled. Unexpectedly, we find Bcl6, previously shown to be involved in the transition of cortical neurons from progenitor to postmitotic differentiation state to provide a major checkpoint regulating neuron survival during late cortical development. We show that Bcl11a is a direct transcriptional regulator of Bcl6. Deletion of Bcl6 exerts death of cortical projection neurons. In turn, reintroduction of Bcl6 into Bcl11a mutants prevents induction of cell death in these neurons. Together, our data identify a novel Bcl11a/Bcl6-dependent molecular pathway in regulation of developmental cell death during corticogenesis.

SUBMITTER: Wiegreffe C 

PROVIDER: S-EPMC9346488 | biostudies-literature | 2022 Aug

REPOSITORIES: biostudies-literature

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Developmental cell death of cortical projection neurons is controlled by a Bcl11a/Bcl6-dependent pathway.

Wiegreffe Christoph C   Wahl Tobias T   Joos Natalie Sophie NS   Bonnefont Jerome J   Liu Pentao P   Britsch Stefan S  

EMBO reports 20220629 8


Developmental neuron death plays a pivotal role in refining organization and wiring during neocortex formation. Aberrant regulation of this process results in neurodevelopmental disorders including impaired learning and memory. Underlying molecular pathways are incompletely determined. Loss of Bcl11a in cortical projection neurons induces pronounced cell death in upper-layer cortical projection neurons during postnatal corticogenesis. We use this genetic model to explore genetic mechanisms by wh  ...[more]

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