粒体自噬
品脱1
RNA剪接
线粒体
生物
细胞生物学
内含子
髓系白血病
线粒体DNA
遗传学
癌症研究
基因
细胞凋亡
自噬
核糖核酸
作者
Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu,Xiaolei Liu
摘要
Splicing factor mutations are common in myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML), but how they alter cellular functions is unclear. We show that the pathogenic SRSF2P95H/+ mutation disrupts the splicing of mitochondrial mRNAs, impairs mitochondrial complex I function, and robustly increases mitophagy. We also identified a mitochondrial surveillance mechanism by which mitochondrial dysfunction modifies splicing of the mitophagy activator PINK1 to remove a poison intron, increasing the stability and abundance of PINK1 mRNA and protein. SRSF2P95H-induced mitochondrial dysfunction increased PINK1 expression through this mechanism, which is essential for survival of SRSF2P95H/+ cells. Inhibition of splicing with a glycogen synthase kinase 3 inhibitor promoted retention of the poison intron, impairing mitophagy and activating apoptosis in SRSF2P95H/+ cells. These data reveal a homeostatic mechanism for sensing mitochondrial stress through PINK1 splicing and identify increased mitophagy as a disease marker and a therapeutic vulnerability in SRSF2P95H mutant MDS and AML.
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