CAND1 binds CRL4 E3 ubiquitin ligase in the nucleus

Stable Identifier
R-HSA-8955245
Type
Reaction [binding]
Species
Homo sapiens
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CRL complexes consist of a cullin protein (CUL1, 2, 3, 4A, 4B, 5, 7 and 9 in humans) and a RING box protein (RBX1 or 2) in addition to one or more substrate binding proteins that confer substrate specificity to the complex (reviewed in Petroski and Deshaies, 2005; Lipkowitz and Weismann, 2011). CRL4 complexes contain CUL4A or CUL4B. Cullin-associated NEDD8-dissociated protein 1 (CAND1, TIP120) is a key assembly factor of Cullin E3 RING ubiquitin ligase (CRL) complexes, acting as a substrate receptor exchange factor. CAND1 binds to the inactive, deneddylated CRL complex through the conserved amino-terminal 3 Cullin repeats of the cullin subunit, which are also required for binding of the substrate binding proteins (Zheng et al, 2002a, b; Liu et al 2002; Min et al, 2003; Goldenberg et al, 2004). In this way, CAND1 binding destabilizes the CRL complex, allowing exchange of the substrate binding protein (Schmidt et al, 2009; Pierce et al, 2013). Neddylation of the CRL complex results in a conformational change that eliminates the CAND1 binding site (Duda et al, 2008; Saha and Deshaies, 2008; Boh et al, 2011).

Literature References
PubMed ID Title Journal Year
18851830 Multimodal activation of the ubiquitin ligase SCF by Nedd8 conjugation

Saha, A, Deshaies, RJ

Mol. Cell 2008
21463634 Neddylation-induced conformational control regulates cullin RING ligase activity in vivo

Boh, BK, Smith, PG, Hagen, T

J. Mol. Biol. 2011
15688063 Function and regulation of cullin-RING ubiquitin ligases

Petroski, MD, Deshaies, RJ

Nat. Rev. Mol. Cell Biol. 2005
12504025 NEDD8 modification of CUL1 dissociates p120(CAND1), an inhibitor of CUL1-SKP1 binding and SCF ligases

Liu, J, Furukawa, M, Matsumoto, T, Xiong, Y

Mol. Cell 2002
21863050 RINGs of good and evil: RING finger ubiquitin ligases at the crossroads of tumour suppression and oncogenesis

Lipkowitz, S, Weissman, AM

Nat. Rev. Cancer 2011
23535662 CSN- and CAND1-dependent remodelling of the budding yeast SCF complex

Zemla, A, Thomas, Y, Kedziora, S, Knebel, A, Wood, NT, Rabut, G, Kurz, T

Nat Commun 2013
12609982 TIP120A associates with cullins and modulates ubiquitin ligase activity

Min, KW, Hwang, JW, Lee, JS, Park, Y, Tamura, TA, Yoon, JB

J. Biol. Chem. 2003
11961546 Structure of the Cul1-Rbx1-Skp1-F boxSkp2 SCF ubiquitin ligase complex

Zheng, N, Schulman, BA, Song, L, Miller, JJ, Jeffrey, PD, Wang, P, Chu, C, Koepp, DM, Elledge, SJ, Pagano, M, Conaway, RC, Conaway, JW, Harper, JW, Pavletich, NP

Nature 2002
23535663 CAND1 controls in vivo dynamics of the cullin 1-RING ubiquitin ligase repertoire

Wu, S, Zhu, W, Nhan, T, Toth, JI, Petroski, MD, Wolf, DA

Nat Commun 2013
19748355 F-box-directed CRL complex assembly and regulation by the CSN and CAND1

Schmidt, MW, McQuary, PR, Wee, S, Hofmann, K, Wolf, DA

Mol. Cell 2009
23453757 Cand1 promotes assembly of new SCF complexes through dynamic exchange of F box proteins

Pierce, NW, Lee, JE, Liu, X, Sweredoski, MJ, Graham, RL, Larimore, EA, Rome, M, Zheng, N, Clurman, BE, Hess, S, Shan, SO, Deshaies, RJ

Cell 2013
15537541 Structure of the Cand1-Cul1-Roc1 complex reveals regulatory mechanisms for the assembly of the multisubunit cullin-dependent ubiquitin ligases

Goldenberg, SJ, Cascio, TC, Shumway, SD, Garbutt, KC, Liu, J, Xiong, Y, Zheng, N

Cell 2004
18805092 Structural insights into NEDD8 activation of cullin-RING ligases: conformational control of conjugation

Duda, DM, Borg, LA, Scott, DC, Hunt, HW, Hammel, M, Schulman, BA

Cell 2008
12504026 CAND1 binds to unneddylated CUL1 and regulates the formation of SCF ubiquitin E3 ligase complex

Zheng, J, Yang, X, Harrell, JM, Ryzhikov, S, Shim, EH, Lykke-Andersen, K, Wei, N, Sun, H, Kobayashi, R, Zhang, H

Mol. Cell 2002
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