Hernáez Bruno, Díaz-Gil Gema, García-Gallo Mónica, Ignacio Quetglas José, Rodríguez-Crespo Ignacio, Dixon Linda, Escribano José M, Alonso Covadonga
Dpto. Biotecnología, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Ctra. de la Coruña Km 7, 28040 Madrid, Spain.
FEBS Lett. 2004 Jul 2;569(1-3):224-8. doi: 10.1016/j.febslet.2004.06.001.
A specific interaction of ASFV p54 protein with 8 kDa light chain cytoplasmic dynein (DLC8) has been previously characterized and this interaction is critical during virus internalization and transport to factory sites. During early phases of infection, the virus induces the initiation of apoptosis triggering activation of caspase-9 and -3. To analyze the role of the structural protein p54 in apoptosis, transient expression experiments of p54 in Vero cells were carried out which resulted in effector caspase-3 activation and apoptosis. Interestingly, p54 mutants, lacking the 13 aa dynein-binding motif lose caspase activation ability and pro-death function of p54. This is the first reported ASFV protein which induces apoptosis.
非洲猪瘟病毒(ASFV)的p54蛋白与8 kDa轻链胞质动力蛋白(DLC8)之间的特异性相互作用此前已被表征,这种相互作用在病毒内化并转运至工厂位点的过程中至关重要。在感染的早期阶段,病毒诱导细胞凋亡的启动,触发半胱天冬酶-9和-3的激活。为了分析结构蛋白p54在细胞凋亡中的作用,在Vero细胞中进行了p54的瞬时表达实验,结果导致效应半胱天冬酶-3激活和细胞凋亡。有趣的是,缺乏13个氨基酸的动力蛋白结合基序的p54突变体失去了半胱天冬酶激活能力和p54的促死亡功能。这是首次报道的诱导细胞凋亡的ASFV蛋白。