Cdc53/cullin and the essential Hrt1 RING-H2 subunit of SCF define a ubiquitin ligase module that activates the E2 enzyme Cdc34

Autor: J. H. Seol, R.M. R. Feldman, W. Zachariae, A. Shevchenko, C. C. Correll, S. Lyapina, Y. Chi, M. Galova, J. Claypool, S. Sandmeyer, K. Nasmyth, R. J. Deshaies
Rok vydání: 1999
Předmět:
F-Box-WD Repeat-Containing Protein 7
Saccharomyces cerevisiae Proteins
Recombinant Fusion Proteins
Ubiquitin-Protein Ligases
Molecular Sequence Data
Cell Cycle Proteins
Biology
Ubiquitin-conjugating enzyme
Medical and Health Sciences
Anaphase-Promoting Complex-Cyclosome
Ligases
SKP Cullin F-Box Protein Ligases
Basic Helix-Loop-Helix Transcription Factors
Genetics
Animals
Humans
Amino Acid Sequence
Cell division control protein 4
Apc11 Subunit
Anaphase-Promoting Complex-Cyclosome

S-Phase Kinase-Associated Proteins
Ubiquitins
Binding Sites
F-Box Proteins
Cullin Proteins
Psychology and Cognitive Sciences
Ubiquitin-Protein Ligase Complexes
Biological Sciences
Sic1
Ubiquitin ligase
Enzyme Activation
Biochemistry
Ubiquitin-Conjugating Enzymes
biology.protein
CUL1
Cullin
Research Paper
Developmental Biology
Zdroj: Seol, JH; Feldman, RMR; Zachariae, W; Shevchenko, A; Correll, CC; Lyapina, S; et al.(1999). Cdc53/cullin and the essential Hrt1 RING-H2 subunit of SCF define a ubiquitin ligase module that activates the E2 enzyme Cdc34. Genes & Development, 13(12), 1614-1626. doi: 10.1101/gad.13.12.1614. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/80t4f490
ISSN: 0890-9369
DOI: 10.1101/gad.13.12.1614
Popis: SCFCdc4 (Skp1, Cdc53/cullin, F-box protein) defines a family of modular ubiquitin ligases (E3s) that regulate diverse processes including cell cycle, immune response, and development. Mass spectrometric analysis of proteins copurifying with Cdc53 identified the RING-H2 finger protein Hrt1 as a subunit of SCF. Hrt1 shows striking similarity to the Apc11 subunit of anaphase-promoting complex. Conditional inactivation of hrt1(ts) results in stabilization of the SCFCdc4 substrates Sic1 and Cln2 and cell cycle arrest at G1/S. Hrt1 assembles into recombinant SCF complexes and individually binds Cdc4, Cdc53 and Cdc34, but not Skp1. Hrt1 stimulates the E3 activity of recombinant SCF potently and enables the reconstitution of Cln2 ubiquitination by recombinant SCFGrr1. Surprisingly, SCF and the Cdc53/Hrt1 subcomplex activate autoubiquitination of Cdc34 E2 enzyme by a mechanism that does not appear to require a reactive thiol. The highly conserved human HRT1 complements the lethality of hrt1Delta, and human HRT2 binds CUL-1. We conclude that Cdc53/Hrt1 comprise a highly conserved module that serves as the functional core of a broad variety of heteromeric ubiquitin ligases.
Databáze: OpenAIRE