Wang Yetao, Hasegawa Mizuho, Imamura Ryu, Kinoshita Takeshi, Kondo Chiaki, Konaka Kenji, Suda Takashi
Center for the Development of Molecular Target Drugs, Cancer Research Institute, Kanazawa University, Kanazawa 920-0934, Japan.
Int Immunol. 2004 Jun;16(6):777-86. doi: 10.1093/intimm/dxh081. Epub 2004 Apr 19.
Recently, a large subfamily of nucleotide-binding and oligomerization domain-containing proteins that have an N-terminal pyrin-like domain and C-terminal leucine-rich repeats has been described. In this study, we identified PYNOD, a novel member of this family that lacks the leucine-rich repeats. We found that human PYNOD mRNA is expressed in various tissues and at high levels in heart, skeletal muscle and brain. It is also expressed in various cell lines, including haematopoietic cell lines. PYNOD oligomerizes and binds to ASC, an adaptor protein that plays a role in apoptotic and inflammatory signal transduction, and to caspase-1 and IL-1beta. PYNOD inhibits apoptosis-associated speck-like protein containing a CARD (ASC)-mediated NF-kappaB activation and apoptosis, and caspase-1-mediated IL-1beta maturation, and it does so in the presence and absence of constitutively active mutants of CARD12 and PYPAF1, which are enhancers of these processes. Thus, PYNOD is a novel regulator of apoptosis and inflammation.
最近,有人描述了一个核苷酸结合和寡聚化结构域蛋白的大亚家族,这些蛋白具有N端的吡啉样结构域和C端富含亮氨酸的重复序列。在本研究中,我们鉴定出PYNOD,它是该家族的一个新成员,缺乏富含亮氨酸的重复序列。我们发现人PYNOD mRNA在多种组织中表达,在心脏、骨骼肌和脑中表达水平较高。它也在多种细胞系中表达,包括造血细胞系。PYNOD发生寡聚化并与ASC(一种在凋亡和炎症信号转导中起作用的衔接蛋白)、caspase-1和IL-1β结合。PYNOD抑制含CARD(ASC)介导的NF-κB激活和凋亡以及caspase-1介导的IL-1β成熟,无论是否存在CARD12和PYPAF1的组成型活性突变体(这些是这些过程的增强子),它都能发挥作用。因此,PYNOD是凋亡和炎症的新型调节因子。