首页> 外文期刊>BMC Plant Biology >Genome-wide analysis of genes encoding core components of the ubiquitin system in soybean ( Glycine max ) reveals a potential role for ubiquitination in host immunity against soybean cyst nematode
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Genome-wide analysis of genes encoding core components of the ubiquitin system in soybean ( Glycine max ) reveals a potential role for ubiquitination in host immunity against soybean cyst nematode

机译:对大豆中泛素系统核心成分编码基因的全基因组分析表明,泛素化在宿主抵抗大豆囊肿线虫的免疫中具有潜在作用

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Ubiquitination is a major post-translational protein modification that regulates essentially all cellular and physiological pathways in eukaryotes. The ubiquitination process typically involves three distinct classes of enzymes, ubiquitin-activating enzyme (E1), ubiquitin-conjugating enzyme (E2) and ubiquitin ligase (E3). To date, a comprehensive identification and analysis of core components comprising of the whole soybean (Glycine max) ubiquitin system (UBS) has not been reported. We performed a systematic, genome-wide analysis of genes that encode core members of the soybean UBS in this study. A total of 1431 genes were identified with high confidence to encode putative soybean UBS components, including 4 genes encoding E1s, 71 genes that encode the E2s, and 1356 genes encoding the E3-related components. Among the E3-encoding genes, 760 encode RING-type E3s, 124 encode U-box domain-containing E3s, and 472 encode F-box proteins. To find out whether the identified soybean UBS genes encode active enzymes, a set of genes were randomly selected and the enzymatic activities of their recombinant proteins were tested. Thioester assays indicated proteins encoded by the soybean E1 gene GmUBA1 and the majority of selected E2 genes are active E1 or E2 enzymes, respectively. Meanwhile, most of the purified RING and U-box domain-containing proteins displayed E3 activity in the in vitro ubiquitination assay. In addition, 1034 of the identified soybean UBS genes were found to express in at least one of 14 soybean tissues examined and the transcript level of 338 soybean USB genes were significantly changed after abiotic or biotic (Fusarium oxysporum and Rhizobium strains) stress treatment. Finally, the expression level of a large number of the identified soybean UBS-related genes was found significantly altered after soybean cyst nematode (SCN) treatment, suggesting the soybean UBS potentially plays an important role in soybean immunity against SCN. Our findings indicate the presence of a large and diverse number of core?UBS proteins in the soybean genome,?which suggests that target-specific modification by ubiquitin is a complex and important part of cellular and physiological regulation in soybean. We also revealed certain members of the soybean UBS may be involved in immunity against soybean cyst nematode (SCN). This study sets up an essential foundation for further functional characterization of the soybean UBS in?various physiological processes, such as?host immunity against SCN.
机译:泛素化是主要的翻译后蛋白质修饰,可调节真核生物中的所有细胞和生理途径。泛素化过程通常涉及三种不同的酶,泛素激活酶(E1),泛素结合酶(E2)和泛素连接酶(E3)。迄今为止,尚未报道对包括整个大豆(大豆最大)泛素系统(UBS)在内的核心成分的全面鉴定和分析。在这项研究中,我们对编码大豆UBS核心成员的基因进行了系统的全基因组分析。总共确定了1431个基因来编码推定的大豆UBS成分,包括4个编码E1的基因,71个编码E2的基因和1356个编码E3相关成分的基因。在E3编码基因中,有760个编码RING型E3,124个编码包含U-box结构域的E3,而472个编码F-box蛋白。为了确定所鉴定的大豆UBS基因是否编码活性酶,随机选择了一组基因,并测试了其重组蛋白的酶活性。硫酯测定表明,由大豆E1基因GmUBA1编码的蛋白质和大多数选定的E2基因分别是活性E1或E2酶。同时,大多数纯化的含有RING和U-box结构域的蛋白质在体外泛素化测定中均显示E3活性。此外,发现在所检查的14个大豆组织中的至少1个中,有1034个已识别的大豆UBS基因表达,并且经过非生物或生物(尖孢镰刀菌和根瘤菌菌株)胁迫处理后,338个大豆USB基因的转录水平发生了显着变化。最后,发现大豆囊肿线虫(SCN)处理后,大量已鉴定的大豆UBS相关基因的表达水平发生了显着变化,这表明大豆UBS可能在大豆抗SCN免疫中发挥重要作用。我们的发现表明大豆基因组中存在大量核心的UBS蛋白,这表明泛素对靶标的特异性修饰是大豆细胞和生理调控的复杂而重要的部分。我们还发现,大豆UBS的某些成员可能参与了针对大豆囊肿线虫(SCN)的免疫。这项研究为大豆UBS在各种生理过程(如宿主对SCN的免疫)中进一步功能表征奠定了重要基础。

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