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MITF Regulates Downstream Genes in Response to Vibrio parahaemolyticus Infection in the Clam Meretrix Petechialis

机译:MITF规管蛤MeMetetrix Petechialis副溶血弧菌感染的下游基因。

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摘要

The microphthalmia-associated transcription factor (MITF) is a basic helix-loop-helix-leucine zipper protein that plays a key role in cell proliferation, survival and immune defense through the direct transcriptional control of downstream genes. We have found that MITF participates in the immune response to Vibrio parahaemolyticus infection in the clam Meretrix petechialis. In this study, we focused on how MITF functions in immunity. First, PO, CTSK, and BCL-2 were identified as the target genes of MpMITF in the clam by RNAi. EMSAs showed direct binding between the MpMITF protein and the E-box of the MpPO, MpCTSK, and MpBCL-2 promoters. Yeast one-hybrid assays also suggested that MpMITF could activate the expression of these three downstream genes. These results demonstrated that the transcriptional expression of MpPO, MpCTSK, and MpBCL-2 is directly regulated by MpMITF. Second, we analyzed the roles of MpPO, MpCTSK, and MpBCL-2 in clam immunity. The mRNA expression of MpPO, MpCTSK, and MpBCL-2 increased significantly after V. parahaemolyticus challenge, which implied that these genes might take part in the immune defense against V. parahaemolyticus challenge in clams. The purified recombinant proteins, MpPO and MpCTSK, inhibited the growth of V. parahaemolyticus. Additionally, the apoptosis rate of clam haemocytes rose significantly when the activity of MpBCL-2 was suppressed. These results revealed that MpPO, MpCTSK, and MpBCL-2 are involved in the immune defense against V. parahaemolyticus. This study supports the idea that the MpMITF pathway plays a key role in immune defense through the direct regulation of the downstream genes MpPO, MpCTSK, and MpBCL-2 in the clam, M. petechialis.
机译:小眼症相关转录因子(MITF)是一种基本的螺旋-环-螺旋-亮氨酸拉链蛋白,通过下游基因的直接转录控制,在细胞增殖,存活和免疫防御中起关键作用。我们发现,MITF参与了蛤MeMeretrix petechialis对副溶血弧菌感染的免疫反应。在这项研究中,我们集中于MITF如何发挥免疫功能。首先,RNAi将PO,CTSK和BCL-2鉴定为蛤中MpMITF的靶基因。 EMSA显示MpMITF蛋白与MpPO,MpCTSK和MpBCL-2启动子的E-box直接结合。酵母一杂交试验还表明,MpMITF可以激活这三个下游基因的表达。这些结果表明,MpMITF直接调控MpPO,MpCTSK和MpBCL-2的转录表达。其次,我们分析了MpPO,MpCTSK和MpBCL-2在蛤类免疫中的作用。副溶血性弧菌攻击后,MpPO,MpCTSK和MpBCL-2的mRNA表达显着增加,这表明这些基因可能参与了蛤中针对副溶血性弧菌攻击的免疫防御。纯化的重组蛋白MpPO和MpCTSK抑制了溶血弧菌的生长。此外,抑制MpBCL-2的活性时,蛤类血细胞的凋亡率显着上升。这些结果表明 MpPO,MpCTSK MpBCL-2 参与了针对 V的免疫防御。副溶血。这项研究支持以下观点:MpMITF途径通过直接调控蛤的下游基因 MpPO,MpCTSK MpBCL-2 在免疫防御中起关键作用, M。 petechialis

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