Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Cell Rep. 2022 Sep 6;40(10):111312. doi: 10.1016/j.celrep.2022.111312.
Down syndrome (DS), driven by an extra copy of chromosome 21 (HSA21), and fragile X syndrome (FXS), driven by loss of the RNA-binding protein FMRP, are two common genetic causes of intellectual disability and autism. Based upon the number of DS-implicated transcripts bound by FMRP, we hypothesize that DS and FXS may share underlying mechanisms. Comparing DS and FXS human pluripotent stem cell (hPSC) and glutamatergic neuron models, we identify increased protein expression of select targets and overlapping transcriptional perturbations. Moreover, acute upregulation of endogenous FMRP in DS patient cells using CRISPRa is sufficient to significantly reduce expression levels of candidate proteins and reverse 40% of global transcriptional perturbations. These results pinpoint specific molecular perturbations shared between DS and FXS that can be leveraged as a strategy for target prioritization; they also provide evidence for the functional relevance of previous associations between FMRP targets and disease-implicated genes.
唐氏综合征(DS)由 21 号染色体(HSA21)的额外拷贝驱动,脆性 X 综合征(FXS)由 RNA 结合蛋白 FMRP 的缺失驱动,是两种常见的智力残疾和自闭症的遗传原因。基于 FMRP 结合的 DS 相关转录本的数量,我们假设 DS 和 FXS 可能具有潜在的机制。通过比较 DS 和 FXS 人类多能干细胞(hPSC)和谷氨酸能神经元模型,我们确定了选定靶标的蛋白表达增加和重叠的转录扰动。此外,在 DS 患者细胞中使用 CRISPRa 急性上调内源性 FMRP 足以显著降低候选蛋白的表达水平,并使 40%的全局转录扰动得到逆转。这些结果指出了 DS 和 FXS 之间共享的特定分子扰动,可作为目标优先级的策略;它们还为 FMRP 靶标和疾病相关基因之间的先前关联的功能相关性提供了证据。