The enzymes of the ubiquitylation pathway play a pivotal role in a number of cellular processes including regulated and targeted proteosomal degradation of substrate proteins. Three classes of enzymes are involved in the process of ubiquitylation; activating enzymes (E1s), conjugating enzymes (E2s) and protein ligases (E3s). UBE2E3 is a member of the E2 ubiquitin-conjugating enzyme family and cloning of the gene was first described by Ito et al. (1999). UBE2E3 binds to the RING-finger proteins ARA54 and RNF8, thought to act as E3 ligases in the ubiquitylation of nuclear proteins (Ito et al., 2001). The epithelial Na+ channel (ENaC) is regulated by UBE2E3 and the E3 ligase NEDD4.2. UBE2E3 interacts with NEDD4.2 via its UBC domain and ubiquitylation of ENaC occurs by NEDD4.2 binding the PY motifs of its α, β and γ subunits (Debonneville and Staub, 2004). NEDD4.2 is a negative regulator of ENaC and deletions in the PY motifs of the β and γ subunits of ENaC cause Liddle’s syndrome, an inherited form of hypertension. The loss of NEDD4.2 binding sites in mutated ENaC causes an increase in channel number at the cell surface and increased Na+ reabsorption by the distal nephron, resulting in hypertension (Abriel et al., 1999).
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Debonneville C, Staub O (2004) Participation of the ubiquitin-conjugating enzyme UBE2E3 in Nedd4-2-dependent regulation of the epithelial Na+ channel. Mol Cell Biol 24, 2397-409.
Ito K, Adachi S, Iwakami R, Yasuda H, Muto Y, Seki N, Okano Y (2001) N-Terminally extended human ubiquitin-conjugating enzymes (E2s) mediate the ubiquitination of RING-finger proteins, ARA54 and RNF8. Eur J Biochem 268, 2725-32.
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