SOCS3 acts as a potential negative regulator in the antiviral response of large yellow croaker (Larimichthys crocea) by interacting with STAT1

IF 5.1 Q1 ENVIRONMENTAL SCIENCES
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Abstract

Suppressors of cytokine signaling (SOCS) proteins are important regulators of the Janus kinase-signal transducer and activator of transcription (JAK-STAT) pathway. Within the SOCS family, SOCS3 is one of the most potent inhibitors of cytokine signaling. However, there is limited knowledge regarding the function of SOCS3 on regulating type I interferon (IFN) signaling in fish. In this study, the complete open reading frame (ORF) of SOCS3 from the large yellow croaker (Larimichthys crocea, LcSOCS3) was cloned and characterized. The ORF of LcSOCS3 was 618 nucleotides in length and encoded a protein containing 205 amino acids. LcSOCS3 had the typical domain architecture of the SOCS family, including an SRC homology 2 (SH2) domain, a SOCS box, an additional kinase inhibition region (KIR), and an extended SH2 subdomain (ESS). Phylogenetic analysis revealed that LcSOCS3 was clustered with other fish SOCS3s and most closely related to the SOCS3 of Collichthy lucidus. LcSOCS3 mRNA was detected in all organs or tissues examined, and its expression was significantly increased in both head kidney and spleen tissues, and primary head kidney leukocytes after poly(I:C) stimulation. Overexpression of LcSOCS3 significantly promoted Spring viremia of carp virus (SVCV) replication, resulting in a more severe cytopathic effect, increased viral titer, enhanced copy number of the SVCV-G gene, and decreased expression levels of IFN1, IRF7, ISG15, Viperin, PKR, and Mx in epithelioma papulosum cyprinid (EPC) cells. Silencing of LcSOCS3 correspondingly up-regulated the expression of IFNi, IFNh, PKR, Viperin, and Mx in large yellow croaker head kidney (LYCK) cells. Additionally, LcSOCS3 was shown to interact with Signal Transducer and Activator of Transcription 1 (STAT1) which may inhibit STAT1 translocating into the nucleus. This speculation was supported by the increased phosphorylation level of STAT1 in head kidney leukocytes after LcSOCS3 silencing. These results indicated that LcSOCS3 functioned as a potential negative regulator of type I IFN signaling in large yellow croaker through its interaction with STAT1.

SOCS3 通过与 STAT1 相互作用成为大黄鱼抗病毒反应的潜在负调控因子
细胞因子信号转导抑制因子(SOCS)蛋白是 Janus 激酶-信号转导和转录激活因子(JAK-STAT)通路的重要调节因子。在 SOCS 家族中,SOCS3 是最有效的细胞因子信号转导抑制剂之一。然而,人们对 SOCS3 调节鱼类 I 型干扰素(IFN)信号传导的功能了解有限。本研究克隆并鉴定了大黄鱼(Larimichthys crocea,LcSOCS3)SOCS3的完整开放阅读框(ORF)。LcSOCS3 的 ORF 长度为 618 个核苷酸,编码一种含有 205 个氨基酸的蛋白质。LcSOCS3具有SOCS家族的典型结构域,包括一个SRC同源2(SH2)结构域、一个SOCS框、一个额外的激酶抑制区(KIR)和一个扩展的SH2亚结构域(ESS)。系统进化分析表明,LcSOCS3 与其他鱼类的 SOCS3 聚类,与 Collichthy lucidus 的 SOCS3 关系最为密切。LcSOCS3的mRNA在所有受检器官或组织中均可检测到,其在头肾和脾脏组织中的表达量显著增加,在poly(I:C)刺激后的头肾原代白细胞中的表达量也显著增加。过表达 LcSOCS3 能显著促进鲤鱼病毒(SVCV)的春季病毒血症复制,导致更严重的细胞病理效应、病毒滴度增加、SVCV-G 基因拷贝数增加,以及上皮乳头状瘤细胞(EPC)中 IFN1、IRF7、ISG15、Viperin、PKR 和 Mx 的表达水平下降。沉默LcSOCS3可相应地上调大黄鱼头肾细胞(LYCK)中IFNi、IFNh、PKR、Viperin和Mx的表达。此外,LcSOCS3 与信号转导和转录激活因子 1(STAT1)相互作用,可能会抑制 STAT1 转位至细胞核。沉默 LcSOCS3 后,头肾白细胞中 STAT1 的磷酸化水平升高,也支持了这一推测。这些结果表明,LcSOCS3 通过与 STAT1 相互作用,成为大黄鱼 I 型 IFN 信号转导的潜在负调控因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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