%0 Journal Article %T CGG repeats in the human FMR1 gene regulate mRNA localization and cellular stress in developing neurons. %A Sirois CL %A Guo Y %A Li M %A Wolkoff NE %A Korabelnikov T %A Sandoval S %A Lee J %A Shen M %A Contractor A %A Sousa AMM %A Bhattacharyya A %A Zhao X %J Cell Rep %V 43 %N 6 %D 2024 Jun 25 %M 38865241 暂无%R 10.1016/j.celrep.2024.114330 %X The human genome has many short tandem repeats, yet the normal functions of these repeats are unclear. The 5' untranslated region (UTR) of the fragile X messenger ribonucleoprotein 1 (FMR1) gene contains polymorphic CGG repeats, the length of which has differing effects on FMR1 expression and human health, including the neurodevelopmental disorder fragile X syndrome. We deleted the CGG repeats in the FMR1 gene (0CGG) in human stem cells and examined the effects on differentiated neurons. 0CGG neurons have altered subcellular localization of FMR1 mRNA and protein, and differential expression of cellular stress proteins compared with neurons with normal repeats (31CGG). In addition, 0CGG neurons have altered responses to glucocorticoid receptor (GR) activation, including FMR1 mRNA localization, GR chaperone HSP90α expression, GR localization, and cellular stress protein levels. Therefore, the CGG repeats in the FMR1 gene are important for the homeostatic responses of neurons to stress signals.