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Feedback regulation of cholesterol uptake by the LXR-IDOL-LDLR axis.
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LXR regulates cholesterol uptake through Idol-dependent ubiquitination of the LDL receptor.
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The E3 ubiquitin ligase IDOL induces the degradation of the low density lipoprotein receptor family members VLDLR and ApoER2.
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Non-Coding RNAs as Critical Modulators of Cholesterol Metabolism in Cancer.
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Endo-lysosomal dysfunction and neuronal-glial crosstalk in Niemann-Pick type C disease.
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Fission yeast Dma1 requires RING domain dimerization for its ubiquitin ligase activity and mitotic checkpoint function.
J Biol Chem. 2012 Jul 27;287(31):25741-8. doi: 10.1074/jbc.M112.349712. Epub 2012 Jun 5.
3
FERM-dependent E3 ligase recognition is a conserved mechanism for targeted degradation of lipoprotein receptors.
Proc Natl Acad Sci U S A. 2011 Dec 13;108(50):20107-12. doi: 10.1073/pnas.1111589108. Epub 2011 Nov 22.
4
Mechanism of ubiquitylation by dimeric RING ligase RNF4.
Nat Struct Mol Biol. 2011 Aug 21;18(9):1052-9. doi: 10.1038/nsmb.2108.
5
The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans.
J Clin Invest. 2011 Aug;121(8):3062-71. doi: 10.1172/JCI45504. Epub 2011 Jul 18.
7
The IDOL-UBE2D complex mediates sterol-dependent degradation of the LDL receptor.
Genes Dev. 2011 Jun 15;25(12):1262-74. doi: 10.1101/gad.2056211.
9
Biological, clinical and population relevance of 95 loci for blood lipids.
Nature. 2010 Aug 5;466(7307):707-13. doi: 10.1038/nature09270.
10
RING domain dimerization is essential for RNF4 function.
Biochem J. 2010 Oct 1;431(1):23-9. doi: 10.1042/BJ20100957.

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