摘要
泛素化修饰是一种蛋白质降解调控的重要途径,而E3泛素连接酶是泛素化系统的关键组分,结合并决定靶标蛋白。前期研究中从大豆中克隆了一个广谱抗病基因SRC7(SMV resistance cluster 7),其主要功能结构域是TN(TIR-NBS)结构域。本氏烟草(Nicotiana benthamiana)中两个编码泛素相关的蛋白NbRGLG2和NbUBXN6均与SRC7^(TN)具有互作。瞬时表达实验中NbRGLG2与NbUBXN6对SMV和TMV无抗性。然而,NbRGLG2与NbUBXN6与SRC7^(TN)共表达时,都会抑制SRC7^(TN)的抗病毒活性。过表达SRC7(Ox-SRC7)本氏烟草中沉默NbRGLG2基因和NbUBXN6基因时,它们可以增强SRC7^(TN)对SMV和TMV的抗性。这些结果显示,NbRGLG2与NbUBXN6负调控SRC7的抗病毒活性。
Ubiquitination is an important pathway for protein degradation,and E3 ligase is a key component of the ubiquitination system,binding to and determining target proteins.In previous research,we cloned a broad-spectrum disease resistance gene SRC7(SMV resistance cluster 7) from soybean,and confirmed that main functional domain of SRC7 was the TN(TIR-NBS) domain.Two ubiquitin-related proteins in Nicotiana benthamiana,NbRGLG2 and NbUBXN6,both interact with SRC7~(TN).In transient expression experiments,NbRGLG2 and NbUBXN6 were not resistant to SMV and TMV.However,when NbRGLG2 and NbUBXN6 are co-expressed with SRC7~(TN),both of them inhibit the antiviral activity of SRC7~(TN).When NbRGLG2 and NbUBXN6 gene were silenced in SRC7 overexpression(Ox-SRC7) plant,they can enhance the resistance of SRC7~(TN) to SMV and TMV.These results show that NbRGLG2 and NbUBXN6 negatively regulate the antiviral activity of SRC7.
作者
李妍楠
纪惠惠
哈达
LI Yannan;JI Huihui;Hada(School of Life Sciences,Inner Mongolia University/Key Laboratory of Forage and Specialty Crop Biology,Ministry of Education/National Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock Co-constructed by the Province and the Ministry,Hohhot 010070,China)
出处
《内蒙古大学学报(自然科学版)》
CAS
2024年第2期193-200,共8页
Journal of Inner Mongolia University:Natural Science Edition
基金
内蒙古自治区科技计划项目(2020GG0045)。