Division of Biology and Biological Engineering, Caltech, Pasadena, United States.
Simons Initiative for the Developing Brain, Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Elife. 2020 Jan 15;9:e52656. doi: 10.7554/eLife.52656.
SynGAP is a postsynaptic density (PSD) protein that binds to PDZ domains of the scaffold protein PSD-95. We previously reported that heterozygous deletion of in mice is correlated with increased steady-state levels of other key PSD proteins that bind PSD-95, although the level of PSD-95 remains constant (Walkup et al., 2016). For example, the ratio to PSD-95 of Transmembrane AMPA-Receptor-associated Proteins (TARPs), which mediate binding of AMPA-type glutamate receptors to PSD-95, was increased in young mice. Here we show that only females and not males show a highly significant correlation between an increase in TARP and a decrease in synGAP in the PSDs of rodents. The data reveal a sex difference in the adaptation of the PSD scaffold to synGAP haploinsufficiency.
SynGAP 是一种突触后密度(PSD)蛋白,与支架蛋白 PSD-95 的 PDZ 结构域结合。我们之前的研究报告表明,在小鼠中杂合缺失与结合 PSD-95 的其他关键 PSD 蛋白的稳态水平增加相关,尽管 PSD-95 的水平保持不变(Walkup 等人,2016)。例如,与 PSD-95 结合的跨膜 AMPA 受体相关蛋白(TARPs)的比率增加,TARPs 介导 AMPA 型谷氨酸受体与 PSD-95 的结合,在年轻小鼠中。在这里,我们表明,只有雌性而不是雄性在 PSD 中的 TARP 增加与 synGAP 减少之间存在高度显著的相关性。这些数据揭示了 PSD 支架对 synGAP 半不足的适应存在性别差异。