Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Broad Institute of MIT and Harvard, and Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
Science. 2014 Feb 14;343(6172):764-8. doi: 10.1126/science.1244392.
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.
人类大脑新皮质有许多功能区域,但其形成机制尚不清楚。在这里,我们描述了 GPR56 调控元件中的一个 15 碱基对缺失突变,该突变通过扰乱区域 GPR56 表达和阻断 RFX 转录因子结合,选择性地破坏了 Sylvian 裂双侧的人类皮质,包括“布罗卡区”,即主要语言区。GPR56 编码一种异三聚体鸟嘌呤核苷酸结合蛋白(G 蛋白)偶联受体,对于正常皮质发育是必需的,并且在皮质祖细胞中表达。GPR56 的表达水平调节祖细胞的增殖。GPR56 的剪接形式在小鼠和人类之间差异很大,而旋毛虫哺乳动物的调控元件指导着局限性的侧皮质表达。我们的数据揭示了一种机制,即通过多个替代启动子控制 GPR56 的表达模式可以影响干细胞增殖、脑回模式,并可能影响新皮质的进化。