Ubiquitin ligases: guardians of mammalian development

DA Cruz Walma, Z Chen, AN Bullock… - … Reviews Molecular Cell …, 2022 - nature.com
Mammalian development demands precision. Millions of molecules must be properly
located in temporal order, and their function regulated, to orchestrate important steps in cell …

The cullin protein family

A Sarikas, T Hartmann, ZQ Pan - Genome biology, 2011 - Springer
Cullin proteins are molecular scaffolds that have crucial roles in the post-translational
modification of cellular proteins involving ubiquitin. The mammalian cullin protein family …

Targeting Cullin–RING E3 ubiquitin ligases for drug discovery: structure, assembly and small-molecule modulation

E Bulatov, A Ciulli - Biochemical Journal, 2015 - portlandpress.com
In the last decade, the ubiquitin–proteasome system has emerged as a valid target for the
development of novel therapeutics. E3 ubiquitin ligases are particularly attractive targets …

The CUL7 E3 ubiquitin ligase targets insulin receptor substrate 1 for ubiquitin-dependent degradation

X Xu, A Sarikas, DC Dias-Santagata, G Dolios… - Molecular cell, 2008 - cell.com
Recent genetic studies have documented a pivotal growth-regulatory role played by the
Cullin 7 (CUL7) E3 ubiquitin ligase complex containing the Fbw8-substrate-targeting …

The GALNT9, BNC1 and CCDC8 genes are frequently epigenetically dysregulated in breast tumours that metastasise to the brain

RP Pangeni, P Channathodiyil, DS Huen, LW Eagles… - Clinical …, 2015 - Springer
Background Tumour metastasis to the brain is a common and deadly development in certain
cancers; 18–30% of breast tumours metastasise to the brain. The contribution that gene …

Cell-intrinsic drivers of dendrite morphogenesis

SV Puram, A Bonni - Development, 2013 - journals.biologists.com
The proper formation and morphogenesis of dendrites is fundamental to the establishment
of neural circuits in the brain. Following cell cycle exit and migration, neurons undergo …

Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth

D Hanson, PG Murray, J O'Sullivan, J Urquhart… - The American Journal of …, 2011 - cell.com
3-M syndrome, a primordial growth disorder, is associated with mutations in CUL7 and
OBSL1. Exome sequencing now identifies mutations in CCDC8 as a cause of 3-M …

Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger–Huët anomaly

N Maksimova, K Hara, I Nikolaeva… - Journal of medical …, 2010 - jmg.bmj.com
Background Hereditary short stature syndromes are clinically and genetically
heterogeneous disorders and the cause have not been fully identified. Yakuts are a …

LATS2 condensates organize signalosomes for Hippo pathway signal transduction

M Qin, E Geng, J Wang, M Yu, T Dong, S Li… - Nature Chemical …, 2024 - nature.com
Biomolecular condensates have been proposed to mediate cellular signaling transduction.
However, the mechanism and functional consequences of signal condensates are not well …

Genetically engineered mouse models for functional studies of SKP1-CUL1-F-box-protein (SCF) E3 ubiquitin ligases

W Zhou, W Wei, Y Sun - Cell research, 2013 - nature.com
Abstract The SCF (SKP1 (S-phase-kinase-associated protein 1), Cullin-1, F-box protein) E3
ubiquitin ligases, the founding member of Cullin-RING ligases (CRLs), are the largest family …