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Norway

PMID:23643363  

Chromatin regulation by BAF170 controls cerebral cortical size and thickness.

Tran Cong Tuoc | Susann Boretius | Stephen N Sansom | Mara-Elena Pitulescu | Jens Frahm | Frederick J Livesey | Anastassia Stoykova
Developmental cell | 2013

Increased cortical size is essential to the enhanced intellectual capacity of primates during mammalian evolution. The mechanisms that control cortical size are largely unknown. Here, we show that mammalian BAF170, a subunit of the chromatin remodeling complex mSWI/SNF, is an intrinsic factor that controls cortical size. We find that conditional deletion of BAF170 promotes indirect neurogenesis by increasing the pool of intermediate progenitors (IPs) and results in an enlarged cortex, whereas cortex-specific BAF170 overexpression results in the opposite phenotype. Mechanistically, BAF170 competes with BAF155 subunit in the BAF complex, affecting euchromatin structure and thereby modulating the binding efficiency of the Pax6/REST-corepressor complex to Pax6 target genes that regulate the generation of IPs and late cortical progenitors. Our findings reveal a molecular mechanism mediated by the mSWI/SNF chromatin-remodeling complex that controls cortical architecture.

Pubmed ID: 23643363

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Associated grants

  • Agency: Wellcome Trust, United Kingdom
    Id: 092096

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