SCFβ-TRCP E3 ubiquitin ligase targets the tumor suppressor ZNRF3 for ubiquitination and degradation
Yanpeng Ci, Xiaoning Li, Maorong Chen, Jiateng Zhong, Brian J. North, Hiroyuki Inuzuka, Xi He, Yu Li, Jianping Guo, Xiangpeng Dai
SCFβ-TRCP E3 ubiquitin ligase targets the tumor suppressor ZNRF3 for ubiquitination and degradation
Wnt signaling has emerged as a major regulator of tissue development by governing the self-renewal and maintenance of stem cells in most tissue types. As a key upstream regulator of the Wnt pathway, the transmembrane E3 ligase ZNRF3 has recently been established to play a role in negative regulation of Wnt signaling by targeting Frizzled (FZD) receptor for ubiquitination and degradation. However, the upstream regulation of ZNRF3, in particular the turnover of ZNRF3, is still unclear. Here we report that ZNRF3 is accumulated in the presence of proteasome inhibitor treatment independent of its E3-ubiquitin ligase activity. Furthermore, the Cullin 1-specific SCF complex containing β-TRCP has been identified to directly interact with and ubiquitinate ZNRF3 thereby regulating its protein stability. Similar with the degradation of β-catenin by β-TRCP, ZNRF3 is ubiquitinated by β-TRCP in both CKI-phosphorylation-and degron-dependent manners. Thus, our findings not only identify a novel substrate for β-TRCP oncogenic regulation, but also highlight the dual regulation of Wnt signaling by β-TRCP in a contextdependent manner where β-TRCP negatively regulates Wnt signaling by targeting β-catenin, and positively regulates Wnt signaling by targeting ZNRF3.
ZNRF3 / β-TRCP / Wnt / ubiquitination / CKI
[1] |
Akhoondi S
CrossRef
Google scholar
|
[2] |
Behrens J
CrossRef
Google scholar
|
[3] |
Busino L
CrossRef
Google scholar
|
[4] |
Clevers H (2006) Wnt/beta-catenin signaling in development and disease. Cell 127:469–480
CrossRef
Google scholar
|
[5] |
de Bie P, Ciechanover A (2011) Ubiquitination of E3 ligases: selfregulation of the ubiquitin system via proteolytic and nonproteolytic mechanisms. Cell Death Differ 18:1393–1402
CrossRef
Google scholar
|
[6] |
Espada J, Calvo MB, Diaz-Prado S, Medina V (2009) Wnt signalling and cancer stem cells. Clin Transl Oncol 11:411–427
CrossRef
Google scholar
|
[7] |
Fuchs SY, Spiegelman VS, Kumar KG (2004) The many faces of beta-TrCP E3 ubiquitin ligases: reflections in the magic mirror of cancer. Oncogene 23:2028–2036
CrossRef
Google scholar
|
[8] |
Gao D
CrossRef
Google scholar
|
[9] |
Goldstein B, Takeshita H, Mizumoto K, Sawa H (2006) Wnt signals can function as positional cues in establishing cell polarity. Dev Cell 10:391–396
CrossRef
Google scholar
|
[10] |
Guardavaccaro D
CrossRef
Google scholar
|
[11] |
Guo J
CrossRef
Google scholar
|
[12] |
Hao HX
CrossRef
Google scholar
|
[13] |
Hart M
CrossRef
Google scholar
|
[14] |
Kimelman D, Xu W (2006) beta-catenin destruction complex: insights and questions from a structural perspective. Oncogene 25:7482–7491
CrossRef
Google scholar
|
[15] |
Koo BK
CrossRef
Google scholar
|
[16] |
Kudo Y
CrossRef
Google scholar
|
[17] |
Lammi L
CrossRef
Google scholar
|
[18] |
Lustig B
CrossRef
Google scholar
|
[19] |
MacDonald BT, He X (2012) Frizzled and LRP5/6 receptors for Wnt/beta-catenin signaling. Cold Spring Harb Perspect Biol 4:12
CrossRef
Google scholar
|
[20] |
Morin PJ
CrossRef
Google scholar
|
[21] |
Nakayama K
CrossRef
Google scholar
|
[22] |
Nusse R, Clevers H (2017) Wnt/beta-catenin signaling, disease, and emerging therapeutic modalities. Cell 169:985–999
CrossRef
Google scholar
|
[23] |
Nusse R, Varmus HE (1982) Many tumors induced by the mouse mammary tumor virus contain a provirus integrated in the same region of the host genome. Cell 31:99–109
CrossRef
Google scholar
|
[24] |
Peifer M, Polakis P (2000) Wnt signaling in oncogenesis and embryogenesis—a look outside the nucleus. Science 287:1606–1609
CrossRef
Google scholar
|
[25] |
Rubinfeld B
CrossRef
Google scholar
|
[26] |
Rubinfeld B
CrossRef
Google scholar
|
[27] |
Saitoh T, Katoh M (2001) Expression profiles of betaTRCP1 and betaTRCP2, and mutation analysis of betaTRCP2 in gastric cancer. Int J Oncol 18:959–964
|
[28] |
Sarikas A, Hartmann T, Pan ZQ (2011) The cullin protein family. Genome Biol 12:220
CrossRef
Google scholar
|
[29] |
Scaglione KM
CrossRef
Google scholar
|
[30] |
Shen M, Schmitt S, Buac D, Dou QP (2013) Targeting the ubiquitinproteasome system for cancer therapy. Expert Opin Ther Targets 17:1091–1108
CrossRef
Google scholar
|
[31] |
Shimizu K
CrossRef
Google scholar
|
[32] |
Skowyra D, Craig KL, Tyers M, Elledge SJ, Harper JW (1997) F-box proteins are receptors that recruit phosphorylated substrates to the SCF ubiquitin-ligase complex. Cell 91:209–219
CrossRef
Google scholar
|
[33] |
Soucy TA
CrossRef
Google scholar
|
[34] |
Sparks AB, Morin PJ, Vogelstein B, Kinzler KW (1998) Mutational analysis of the APC/beta-catenin/Tcf pathway in colorectal cancer. Cancer Res 58:1130–1134
|
[35] |
Spencer E, Jiang J, Chen ZJ (1999) Signal-induced ubiquitination of IkappaBalpha by the F-box protein Slimb/beta-TrCP. Genes Dev 13:284–294
CrossRef
Google scholar
|
[36] |
Spranger S, Bao R, Gajewski TF (2015) Melanoma-intrinsic betacatenin signalling prevents anti-tumour immunity. Nature 523:231–235
CrossRef
Google scholar
|
[37] |
Toomes C
CrossRef
Google scholar
|
[38] |
Van Wesenbeeck L
CrossRef
Google scholar
|
[39] |
Wang Z, Liu P, Inuzuka H, Wei W (2014) Roles of F-box proteins in cancer. Nat Rev Cancer 14:233–247
CrossRef
Google scholar
|
[40] |
Wang Z
CrossRef
Google scholar
|
[41] |
Welcker M, Clurman BE (2008) FBW7 ubiquitin ligase: a tumour suppressor at the crossroads of cell division, growth and differentiation. Nat Rev Cancer 8:83–93
CrossRef
Google scholar
|
[42] |
Westbrook TF
CrossRef
Google scholar
|
[43] |
Yang K
CrossRef
Google scholar
|
/
〈 | 〉 |