Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Apr 21;21(8):2894.
doi: 10.3390/ijms21082894.

The Ubiquitin Conjugating Enzyme: An Important Ubiquitin Transfer Platform in Ubiquitin-Proteasome System

Affiliations
Free PMC article
Review

The Ubiquitin Conjugating Enzyme: An Important Ubiquitin Transfer Platform in Ubiquitin-Proteasome System

Weigang Liu et al. Int J Mol Sci. .
Free PMC article

Abstract

Owing to a sessile lifestyle in nature, plants are routinely faced with diverse hostile environments such as various abiotic and biotic stresses, which lead to accumulation of free radicals in cells, cell damage, protein denaturation, etc., causing adverse effects to cells. During the evolution process, plants formed defense systems composed of numerous complex gene regulatory networks and signal transduction pathways to regulate and maintain the cell homeostasis. Among them, ubiquitin-proteasome pathway (UPP) is the most versatile cellular signal system as well as a powerful mechanism for regulating many aspects of the cell physiology because it removes most of the abnormal and short-lived peptides and proteins. In this system, the ubiquitin-conjugating enzyme (E2) plays a critical role in transporting ubiquitin from the ubiquitin-activating enzyme (E1) to the ubiquitin-ligase enzyme (E3) and substrate. Nevertheless, the comprehensive study regarding the role of E2 enzymes in plants remains unexplored. In this review, the ubiquitination process and the regulatory role that E2 enzymes play in plants are primarily discussed, with the focus particularly put on E2's regulation of biological functions of the cell.

Keywords: E2 functions; ubiquitin; ubiquitin-conjugating enzyme (E2); ubiquitin-proteasome system.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
The ubiquitin-proteasome system. The process of ubiquitination from activation to attachment to the substrate is catalyzed by three major enzymes. The substrates labeled by ubiquitin are degraded by the 26S proteasome or play a non-degradative role in other processes. Abbreviations: APC, Anaphase-promoting complex; DUBs, Deubiquitinating enzymes; E1, Ubiquitin-activating enzyme; E2, Ubiquitin-conjugating enzyme; E3, Ubiquitin-ligase enzyme; Cul-based, Cullin-RING box1-Ligase; HECT, Homology to E6-AP C Terminus; Ub, Ubiqitin; SUMO, Small ubiquitin-related modifier; RBX1, RING-Box 1; RING, Really interesting new gene; RBR, RING1-IBR(cysteine/histidine rich region)-RING2.
Figure 2
Figure 2
The role of UBC13 in DNA damage responses and UBC13′s other functions. (A) UBC13 is involved in post-replication repair (PRR). (B) UBC13 participates in different biological processes by mediating Lys63-linked ubiquitination. Abbreviations: Aux/IAA, Auxin/indole-3-acetic acid; DDT, DNA damage tolerance; ERAD, ER-associated degradation; Mms2, A Ubc E2 variant; PRR, Postreplication repair; PCNA, Proliferating cell nuclear antigen; RGLG1/2, An E3 ligase; RNF5, RING finger protein 5; Rad5, An E3 enzyme; Rad6, An E2 enzyme; Rad18, An E3 enzyme; Suv, Fni3 (Fen-interacting protein, Fen is the host protein kinase) cofactor S. lycoperiscum Uev; Siz1, An E3 ligase; Srs2, A helicase; TLS, Translesion DNA synthesis; Ubc9, An E2 enzyme.

Similar articles

Cited by

References

    1. Ciehanover A., Hod Y., Hershko A. A heat-stable polypeptide component of an ATP-dependent proteolytic system from reticulocytes. Biochem. Biophys. Res. Commun. 1978;81:1100–1105. doi: 10.1016/0006-291X(78)91249-4. - DOI - PubMed
    1. Callis J. The ubiquitination machinery of the ubiquitin system. Arab. Book Am. Soc. Plant Biol. 2014;12:e0174. doi: 10.1199/tab.0174. - DOI - PMC - PubMed
    1. Ciechanover A., Heller H., Elias S., Haas A.L., Hershko A. ATP-dependent conjugation of reticulocyte proteins with the polypeptide required for protein degradation. Proc. Natl. Acad. Sci. USA. 1980;77:1365. doi: 10.1073/pnas.77.3.1365. - DOI - PMC - PubMed
    1. Ciechanover A., Elias S., Heller H., Ferber S., Hershko A. Characterization of the heat-stable polypeptide of the ATP-dependent proteolytic system from reticulocytes. J. Biol. Chem. 1980;255:7525–7528. - PubMed
    1. Wilkinson K.D. The discovery of ubiquitin-dependent proteolysis. Proc. Natl. Acad. Sci. USA. 2005;102:15280. doi: 10.1073/pnas.0504842102. - DOI - PMC - PubMed

Substances