Nature communications · 2026
Bclaf1 drives heart failure by recruiting Srsf2 to enhance Hand2 pre-mRNA splicing and pathological hypertrophy.
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Zhang Yang, Gao Haiyu, Lu Ying, Zhang Yingzi, Yang Meng, Zhang Xiaofang, Zhao Yinfeng, Yu Liying, Zhai Yinghe, Wang Shuang, Zhao Lexin, Yang Guohui, Li Jialiang, Yu Jiaxin, Li Chenhong, Li Changzhu, Wang Yifan, Yang Ying, Li Yue, Yu Luyang, Zhao Deli, Yang Lida, Jiao Lei, Yang Baofeng, Lu Yanjie, Pan Zhenwei
Аннотация
Heart failure with reduced ejection fraction (HFrEF) remains a major therapeutic challenge. B-cell lymphoma 2-associated transcription factor 1 (Bclaf1) is implicated in RNA splicing and cardiac disease, but its role in HFrEF pathogenesis is unknown. Here, we demonstrate that Bclaf1 expression is elevated in human HFrEF myocardium and in male murine pressure-overload models. Cardiac-specific Bclaf1 overexpression drives pathological hypertrophy and systolic dysfunction, whereas its genetic knockout or adeno-associated virus serotype 9 (AAV9)-mediated knockdown attenuates these phenotypes. Mechanistically, Bclaf1 interacts with the splicing factor serine/arginine-rich splicing factor 2 (Srsf2) to bind to heart and neural crest derivatives expressed 2 (Hand2) pre-mRNA and enhance its splicing efficiency, leading to increased mature Hand2 levels and maladaptive remodeling. Inhibition of either Bclaf1 or Hand2 rescues cardiac function and structure in experimental HFrEF. Our work defines a Bclaf1/Srsf2/Hand2 splicing axis as a critical driver of HFrEF and reveals a promising therapeutic target for heart failure.