TABLE 1.
Modification types | Regulative sites | Enzymes | Effects |
Phosphorylation | Ser109 | LATS1/2 | YAP1/TAZ cytoplasm retention (Zhao et al., 2010) |
Ser127 (Ser89 in TAZ) | LATS1/2 | Binding YAP1 to 14-3-3 and inducing cytoplasm retention (Zhao et al., 2007) | |
Ser128 | NLK | Blocking YAP1 binding to 14-3-3 (Moon et al., 2017) | |
Ser381 (Ser311 in TAZ) | LATS1/2 | β–Trcp-dependent ubiquitination degradation (Zhao et al., 2010) | |
NS | PRP4K | YAP1/TAZ nuclear export (Cho et al., 2018) | |
Tyr357 | c-Abl | Stabilizing YAP1 stable and increasing YAP1–p73 interaction inducing cell apoptosis (Levy et al., 2008) | |
Tyr357 | Src | Enhancing YAP1 nuclear retention and target gene CTGF expression (Taniguchi et al., 2015) | |
one or more tyrosine residues | Yes | Promoting YAP1 translocation and Oct-3/4 transcription (Tamm et al., 2011) | |
Dephosphorylation | Ser127 (Ser89 and Ser311 in TAZ) | PP1A | YAP1/TAZ nuclear translocation (Liu et al., 2011; Wang et al., 2011). |
O-GlcNacylation | Ser109 | OGT | Impeding LATS1/2-induced YAP1 Ser109 phosphorylation and potentiating YAP1 activity (Peng et al., 2017) |
Thr241 | OGT | Attenuating LATS1/2-dependent YAP1 Ser127 phosphorylation and enhancing YAP1 activity (Zhang et al., 2017) | |
Methylation | Lys342 | SET1A | Dampening YAP1–CRM1 fusion and enhancing YAP1 nuclear retention (Fang et al., 2018) |
Lys494 | SET7 | Enhancing YAP1 translocation to cytosol and cytoplasmic membrane Oudhoff et al., 2013) | |
Ubiquitination | NS | SCFβ–TRCP | YAP1/TAZ protein degradation (Dong et al., 2007; Zhao et al., 2007) |
NS | Fbxw7 | YAP1 protein degradation (Tu et al., 2014; Zhang et al., 2016) | |
Lys321, Lys497 | SKP2 | Accumulating YAP1 nuclear localization and association between YAP1 and TEAD (Yao et al., 2018) | |
De-ubiquitination | NS | USP9X | Stabilizing YAP1 and enhancing its activity (Li et al., 2018a). |
NS | OTUD1 | Reducing YAP1 stability and attenuating the cell proliferation activity of YAP1 (Yao et al., 2018). |
NS, not specified, where the specific regulator sites have not been validated.