解旋酶
RNA解旋酶A
化学
核糖核酸
应力颗粒
细胞生物学
ATP酶
突变
RNA结合蛋白
生物化学
平衡
拉福拉病
生物
AAA蛋白
结合位点
分子生物学
谷氨酸受体
死盒子
遗传学
病理生理学
支架蛋白
作者
Ivan Rosa e Silva,Paula F. V. do Prado,Felipe Zanghelini Benevenutti,Renata Rocha de Oliveira,Aline R. Passos,Camila Canateli,Isabelly Gonçalves Messias,Daniel M. Trindade,Leandro Oliveira Bortot,João V. S. Guerra,Thaís Hancio,Maurício L. Sforça,Andrey F. Z. Nascimento,Gustavo Fernando Mercaldi,Jose Pereira,Matheus C. Fonseca,Paulo S. L. de Oliveira,Murilo de Carvalho,Juliana H. C. Smetana,Ana C. V. Krepischi
出处
期刊:Science Signaling
[American Association for the Advancement of Science]
日期:2026-03-24
卷期号:19 (930)
标识
DOI:10.1126/scisignal.adv4376
摘要
Cl − homeostasis is pivotal during neurodevelopment and in multiple processes in mature neurons, and its disruption is implicated in several neurodevelopmental disorders. Here, we investigated the role of Cl − in regulating DDX3X, an ATP-dependent RNA helicase that is associated with a neurodevelopmental disorder and is involved in stress granule assembly through biomolecular condensation. Cl − directly interacted with the DDX3X helicase core in the RNA binding region. This interaction impaired both ATPase and RNA helicase activities at physiologically relevant concentrations in a manner similar to inorganic phosphate and disrupted its condensation propensity in vitro. In neuroblastoma cells, Cl − efflux induced the formation of large, persistent DDX3X-containing stress granules. Furthermore, the R326H mutation, which is linked to a severe neurodevelopmental disorder, altered the chemical environment of the Cl − -binding site and impaired Cl − -sensitive functions. Together, our findings demonstrate that Cl − binding regulates DDX3X functions and provide insights into the molecular pathophysiology of a neurodevelopmental disorder–linked mutation in DDX3X.
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