4.8 Article

Evolutionarily Dynamic Alternative Splicing of GPR56 Regulates Regional Cerebral Cortical Patterning

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SCIENCE
卷 343, 期 6172, 页码 764-768

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AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1244392

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资金

  1. Medical Research Council [G0700089]
  2. Wellcome Trust Human Developmental Biology Resource [GR082557]
  3. National Institute of Child Health and Human Development, NIH, Brain and Tissue Bank at the University of Maryland [HHSN275200900011C, NO1-HD-9-0011]
  4. Strategic Research Program for Brain Sciences
  5. Ministry of Education, Culture, Sports, Science and Technology (MEXT) Japan
  6. Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST Program)
  7. National Institute of Mental Health, NIH [U01MH081896]
  8. National Institute of Neurological Disorders and Stroke, NIH [2R01NS035129]
  9. Paul G. Allen Family Foundation
  10. Medical Research Council [G0700089, MC_PC_15004] Funding Source: researchfish
  11. MRC [MC_PC_15004, G0700089] Funding Source: UKRI

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The human neocortex has numerous specialized functional areas whose formation is poorly understood. Here, we describe a 15-base pair deletion mutation in a regulatory element of GPR56 that selectively disrupts human cortex surrounding the Sylvian fissure bilaterally including Broca's area, the primary language area, by disrupting regional GPR56 expression and blocking RFX transcription factor binding. GPR56 encodes a heterotrimeric guanine nucleotide-binding protein (G protein)-coupled receptor required for normal cortical development and is expressed in cortical progenitor cells. GPR56 expression levels regulate progenitor proliferation. GPR56 splice forms are highly variable between mice and humans, and the regulatory element of gyrencephalic mammals directs restricted lateral cortical expression. Our data reveal a mechanism by which control of GPR56 expression pattern by multiple alternative promoters can influence stem cell proliferation, gyral patterning, and, potentially, neocortex evolution.

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