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二倍体同源基因协同负调控六倍体吉富罗非鱼 RLR 介导的 IFN 反应。

Two Duplicated Homeologs Cooperatively and Negatively Regulate RLR-Mediated IFN Response in Hexaploid Gibel Carp.

机构信息

State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, The Innovative Academy of Seed Design, Chinese Academy of Sciences, Wuhan, China.

College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China.

出版信息

Front Immunol. 2021 Nov 26;12:780667. doi: 10.3389/fimmu.2021.780667. eCollection 2021.

Abstract

Src homology region 2 domain-containing phosphatase 1 (SHP1), encoded by the () gene, belongs to the family of protein tyrosine phosphatases (PTPs) and participates in multiple signaling pathways of immune cells. However, the mechanism of SHP1 in regulating fish immunity is largely unknown. In this study, we first identified two gibel carp () homeologs ( and ), each of which had three alleles with high identities. Then, relative to , dominant expression in adult tissues and higher upregulated expression of induced by polyinosinic-polycytidylic acid (poly I:C), poly deoxyadenylic-deoxythymidylic (dA:dT) acid and spring viremia of carp virus (SVCV) were uncovered. Finally, we demonstrated that SHP1-A (encoded by the gene) and SHP1-B (encoded by the gene) act as negative regulators of the RIG-I-like receptor (RLR)-mediated interferon (IFN) response two mechanisms: the inhibition of TBK1-induced phosphorylation of MITA shared by SHP1-A and SHP1-B, and the autophagic degradation of MITA exclusively by SHP1-A. Meanwhile, the data support that SHP1-A and SHP1-B have sub-functionalized and that SHP1-A overwhelmingly dominates SHP1-B in the process of RLR-mediated IFN response. The current study not only sheds light on the regulative mechanism of SHP1 in fish immunity, but also provides a typical case of duplicated gene evolutionary fates.

摘要

Src 同源结构域 2 区磷酸酶 1(SHP1)由基因编码,属于蛋白酪氨酸磷酸酶(PTP)家族,参与免疫细胞的多种信号通路。然而,SHP1 调节鱼类免疫的机制在很大程度上尚不清楚。在本研究中,我们首先鉴定了两种鲤鱼()的同系物(和),每个同系物都有三个高度同源的等位基因。然后,与相比,在成年组织中呈显性表达,poly I:C、poly dA:dT 和鲤春病毒血症病毒(SVCV)诱导的表达上调更高。最后,我们证明了 SHP1-A(由基因编码)和 SHP1-B(由基因编码)作为 RIG-I 样受体(RLR)介导的干扰素(IFN)反应的负调节剂,通过两种机制发挥作用:SHP1-A 和 SHP1-B 共同抑制 TBK1 诱导的 MITA 磷酸化,以及 SHP1-A 特异性的 MITA 自噬降解。同时,数据支持 SHP1-A 和 SHP1-B 具有亚功能化,并且在 RLR 介导的 IFN 反应过程中 SHP1-A 压倒性地占主导地位。本研究不仅揭示了 SHP1 在鱼类免疫中的调节机制,而且为复制基因的进化命运提供了一个典型案例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca2d/8662705/2259b965ec2f/fimmu-12-780667-g001.jpg

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