Department of Psychiatry, Langley Porter Psychiatric Institute, UCSF Weill Institute for Neurosciences, University of California, San Francisco, CA, USA.
Department of Psychiatry, Langley Porter Psychiatric Institute, UCSF Weill Institute for Neurosciences, University of California, San Francisco, CA, USA.
Cell Rep. 2021 Dec 7;37(10):110089. doi: 10.1016/j.celrep.2021.110089.
Deleterious genetic variants in POGZ, which encodes the chromatin regulator Pogo Transposable Element with ZNF Domain protein, are strongly associated with autism spectrum disorder (ASD). Although it is a high-confidence ASD risk gene, the neurodevelopmental functions of POGZ remain unclear. Here we reveal the genomic binding of POGZ in the developing forebrain at euchromatic loci and gene regulatory elements (REs). We profile chromatin accessibility and gene expression in Pogz mice and show that POGZ promotes the active chromatin state and transcription of clustered synaptic genes. We further demonstrate that POGZ forms a nuclear complex and co-occupies loci with ADNP, another high-confidence ASD risk gene, and provide evidence that POGZ regulates other neurodevelopmental disorder risk genes as well. Our results reveal a neurodevelopmental function of an ASD risk gene and identify molecular targets that may elucidate its function in ASD.
编码染色质调节因子 Pogo 转座元件锌指蛋白的 POGZ 中的有害遗传变异与自闭症谱系障碍(ASD)强烈相关。尽管它是一种高可信度的 ASD 风险基因,但 POGZ 的神经发育功能仍不清楚。在这里,我们揭示了 POGZ 在常染色质位置和基因调控元件(RE)中发育前脑的基因组结合。我们对 Pogz 小鼠进行了染色质可及性和基因表达分析,结果表明 POGZ 促进了簇状突触基因的活跃染色质状态和转录。我们进一步证明 POGZ 形成核复合物,并与另一个高可信度的 ASD 风险基因 ADNP 共同占据基因座,并提供证据表明 POGZ 还调节其他神经发育障碍风险基因。我们的研究结果揭示了 ASD 风险基因的神经发育功能,并确定了可能阐明其在 ASD 中功能的分子靶标。