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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

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          Abstract

          Background

          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.

          Results

          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.

          Conclusions

          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.

          Electronic supplementary material

          The online version of this article (10.1186/s12870-018-1365-7) contains supplementary material, which is available to authorized users.

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          Most cited references75

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          HMMER web server: 2015 update

          The HMMER website, available at http://www.ebi.ac.uk/Tools/hmmer/, provides access to the protein homology search algorithms found in the HMMER software suite. Since the first release of the website in 2011, the search repertoire has been expanded to include the iterative search algorithm, jackhmmer. The continued growth of the target sequence databases means that traditional tabular representations of significant sequence hits can be overwhelming to the user. Consequently, additional ways of presenting homology search results have been developed, allowing them to be summarised according to taxonomic distribution or domain architecture. The taxonomy and domain architecture representations can be used in combination to filter the results according to the needs of a user. Searches can also be restricted prior to submission using a new taxonomic filter, which not only ensures that the results are specific to the requested taxonomic group, but also improves search performance. The repertoire of profile hidden Markov model libraries, which are used for annotation of query sequences with protein families and domains, has been expanded to include the libraries from CATH-Gene3D, PIRSF, Superfamily and TIGRFAMs. Finally, we discuss the relocation of the HMMER webserver to the European Bioinformatics Institute and the potential impact that this will have.
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            The ubiquitin-26S proteasome system at the nexus of plant biology.

            Plants, like other eukaryotes, rely on proteolysis to control the abundance of key regulatory proteins and enzymes. Strikingly, genome-wide studies have revealed that the ubiquitin-26S proteasome system (UPS) in particular is an exceedingly large and complex route for protein removal, occupying nearly 6% of the Arabidopsis thaliana proteome. But why is the UPS so pervasive in plants? Data accumulated over the past few years now show that it targets numerous intracellular regulators that have central roles in hormone signalling, the regulation of chromatin structure and transcription, tailoring morphogenesis, responses to environmental challenges, self recognition and battling pathogens.
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              Physiological functions of the HECT family of ubiquitin ligases.

              The ubiquitylation of proteins is carried out by E1, E2 and E3 (ubiquitin ligase) enzymes, and targets them for degradation or for other cellular fates. The HECT enzymes, including Nedd4 family members, are a major group of E3 enzymes that dictate the specificity of ubiquitylation. In addition to ubiquitylating proteins for degradation by the 26S proteasome, HECT E3 enzymes regulate the trafficking of many receptors, channels, transporters and viral proteins. The physiological functions of the yeast HECT E3 ligase Rsp5 are the best known, but the functions of HECT E3 enyzmes in metazoans are now becoming clearer from in vivo studies.
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                Author and article information

                Contributors
                czhang49@unl.edu
                lisong0426@gmail.com
                manikant.choudhary@gmail.com
                bzhou3@unl.edu
                guangchao.sun@unl.edu
                kbroderick2@unl.edu
                loren.giesler@unl.edu
                lzeng3@unl.edu
                Journal
                BMC Plant Biol
                BMC Plant Biol
                BMC Plant Biology
                BioMed Central (London )
                1471-2229
                18 July 2018
                18 July 2018
                2018
                : 18
                : 149
                Affiliations
                [1 ]ISNI 0000 0004 1937 0060, GRID grid.24434.35, Department of Plant Pathology, , University of Nebraska, ; Lincoln, NE 68583 USA
                [2 ]ISNI 0000 0004 1937 0060, GRID grid.24434.35, Center for Plant Science Innovation, , University of Nebraska, ; Lincoln, NE 68588 USA
                [3 ]ISNI 0000 0000 9068 3546, GRID grid.194632.b, Department of Information Science, , University of Arkansas, ; Little Rock, AR 72204 USA
                [4 ]ISNI 0000 0004 1937 0060, GRID grid.24434.35, Department of Agronomy and Horticulture, , University of Nebraska, ; Lincoln, NE 68583 USA
                Author information
                http://orcid.org/0000-0001-8802-4872
                Article
                1365
                10.1186/s12870-018-1365-7
                6052599
                30021519
                36813e80-3fab-467f-a959-e9f7b8b44771
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 1 December 2017
                : 9 July 2018
                Funding
                Funded by: Nebraska Soybean Board
                Award ID: 1719
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2018

                Plant science & Botany
                soybean,ubiquitin system (ubs),ubiquitin-activating enzyme (e1),ubiquitin-conjugating enzyme (e2),ring domain,u-box domain,f-box domain,soybean cyst nematode,immunity

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