Duran Javier, Nickel Lennart, Estrada Manuel, Backs Johannes, van den Hoogenhof Maarten M G
Institute of Experimental Cardiology, Heidelberg University, Heidelberg, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Heidelberg/Mannheim, Heidelberg, Germany.
Front Cell Dev Biol. 2021 Mar 11;9:644630. doi: 10.3389/fcell.2021.644630. eCollection 2021.
RNA splicing has been recognized in recent years as a pivotal player in heart development and disease. The Ca/calmodulin dependent protein kinase II delta (CaMKIIδ) is a multifunctional Ser/Thr kinase family and generates at least 11 different splice variants through alternative splicing. This enzyme, which belongs to the CaMKII family, is the predominant family member in the heart and functions as a messenger toward adaptive or detrimental signaling in cardiomyocytes. Classically, the nuclear CaMKIIδB and cytoplasmic CaMKIIδC splice variants are described as mediators of arrhythmias, contractile function, Ca handling, and gene transcription. Recent findings also put CaMKIIδA and CaMKIIδ9 as cardinal players in the global CaMKII response in the heart. In this review, we discuss and summarize the new insights into CaMKIIδ splice variants and their (proposed) functions, as well as CaMKII-engineered mouse phenotypes and cardiac dysfunction related to CaMKIIδ missplicing. We also discuss RNA splicing factors affecting CaMKII splicing. Finally, we discuss the translational perspective derived from these insights and future directions on CaMKIIδ splicing research in the healthy and diseased heart.
近年来,RNA剪接已被公认为心脏发育和疾病中的关键因素。钙/钙调蛋白依赖性蛋白激酶IIδ(CaMKIIδ)是一个多功能丝氨酸/苏氨酸激酶家族,通过可变剪接产生至少11种不同的剪接变体。这种属于CaMKII家族的酶是心脏中的主要家族成员,在心肌细胞中作为适应性或有害信号的信使发挥作用。传统上,核CaMKIIδB和细胞质CaMKIIδC剪接变体被描述为心律失常、收缩功能、钙处理和基因转录的介质。最近的研究结果还表明,CaMKIIδA和CaMKIIδ9是心脏整体CaMKII反应的主要参与者。在这篇综述中,我们讨论并总结了关于CaMKIIδ剪接变体及其(推测的)功能的新见解,以及与CaMKIIδ错配剪接相关的CaMKII工程小鼠表型和心脏功能障碍。我们还讨论了影响CaMKII剪接的RNA剪接因子。最后,我们讨论了从这些见解中得出的转化前景以及健康和患病心脏中CaMKIIδ剪接研究的未来方向。