HdmX stimulates Hdm2-mediated ubiquitination and degradation of p53


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LINARES, Laëtitia K., Arnd HENGSTERMANN, Aaron CIECHANOVER, Stefan MÜLLER, Martin SCHEFFNER, 2003. HdmX stimulates Hdm2-mediated ubiquitination and degradation of p53. In: Proceedings of the National Academy of Sciences. 100(21), pp. 12009-12014. ISSN 0027-8424

@article{Linares2003-10-14stimu-16757, title={HdmX stimulates Hdm2-mediated ubiquitination and degradation of p53}, year={2003}, doi={10.1073/pnas.2030930100}, number={21}, volume={100}, issn={0027-8424}, journal={Proceedings of the National Academy of Sciences}, pages={12009--12014}, author={Linares, Laëtitia K. and Hengstermann, Arnd and Ciechanover, Aaron and Müller, Stefan and Scheffner, Martin} }

<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/16757"> <dc:contributor>Scheffner, Martin</dc:contributor> <dcterms:bibliographicCitation>Publ. in: Proceedings of the National Academy of Sciences of the United States of America ; 100 (2003), 21. - pp. 12009-12014</dcterms:bibliographicCitation> <dcterms:rights rdf:resource="http://nbn-resolving.org/urn:nbn:de:bsz:352-20140905103605204-4002607-1"/> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/16757"/> <dc:creator>Scheffner, Martin</dc:creator> <dc:creator>Linares, Laëtitia K.</dc:creator> <dcterms:title>HdmX stimulates Hdm2-mediated ubiquitination and degradation of p53</dcterms:title> <dc:creator>Hengstermann, Arnd</dc:creator> <dcterms:issued>2003-10-14</dcterms:issued> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-11-16T09:24:11Z</dcterms:available> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-11-16T09:24:11Z</dc:date> <dc:contributor>Linares, Laëtitia K.</dc:contributor> <dc:contributor>Müller, Stefan</dc:contributor> <dc:contributor>Ciechanover, Aaron</dc:contributor> <dcterms:abstract xml:lang="eng">The RING finger proteins HdmX and Hdm2 share significant structural and functional similarity. Hdm2 is a member of the RING finger family of ubiquitin-protein ligases E3 and targets the tumor suppressor protein p53 for degradation. Although HdmX also binds to p53, HdmX does not induce p53 degradation. Moreover, HdmX has been reported to interfere with p53 degradation in overexpression experiments. To obtain insight into the mechanism by which HdmX interferes with p53 degradation, we studied the effect of HdmX on the E3 activity of Hdm2 in vitro. Surprisingly, this revealed that HdmX stimulates Hdm2-mediated ubiquitination of p53 and that HdmX facilitates ubiquitination of Hdm2 and vice versa. In addition, down-regulation of HdmX expression within cells results in the accumulation of both p53 and Hdm2. Because HdmX alone does not have appreciable E3 activity, these data indicate that HdmX acts as a stimulator, rather than as an inhibitor, of the E3 activity of Hdm2 and that, at least under certain conditions, HdmX is actively involved in the degradation of both p53 and Hdm2.</dcterms:abstract> <dc:rights>deposit-license</dc:rights> <dc:language>eng</dc:language> <dc:creator>Ciechanover, Aaron</dc:creator> <dc:contributor>Hengstermann, Arnd</dc:contributor> <dc:creator>Müller, Stefan</dc:creator> </rdf:Description> </rdf:RDF>

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