Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase.
Data(s) |
2008
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Resumo |
Williams-Beuren syndrome (WBS) is a neurodevelopmental and multisystemic disease that results from hemizygosity of approximately 25 genes mapping to chromosomal region 7q11.23. We report here the preliminary description of eight novel genes mapping within the WBS critical region and/or its syntenic mouse region. Three of these genes, TRIM50, TRIM73 and TRIM74, belong to the TRIpartite motif gene family, members of which were shown to be associated to several human genetic diseases. We describe the preliminary functional characterization of these genes and show that Trim50 encodes an E3 ubiquitin ligase, opening the interesting hypothesis that the ubiquitin-mediated proteasome pathway might be involved in the WBS phenotype. |
Identificador |
https://serval.unil.ch/notice/serval:BIB_C1B799B255F6 info:pmid:18398435 https://serval.unil.ch/resource/serval:BIB_C1B799B255F6.P001/REF http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_C1B799B255F66 urn:nbn:ch:serval-BIB_C1B799B255F66 |
Idioma(s) |
eng |
Fonte |
European Journal of Human Genetics1691038-1049 |
Palavras-Chave | #Amino Acid Motifs/genetics; Animals; COS Cells; Cell Line, Tumor; Cercopithecus aethiops; Chromosomes, Human, Pair 7/enzymology; Chromosomes, Human, Pair 7/genetics; Hela Cells; Humans; Mice; Phenotype; Proteasome Endopeptidase Complex/physiology; Signal Transduction/genetics; Synteny/genetics; Ubiquitin/physiology; Ubiquitin-Protein Ligases/genetics; Williams Syndrome/enzymology; Williams Syndrome/genetics |
Tipo |
info:eu-repo/semantics/article article |
Formato |
application/pdf |
Direitos |
info:eu-repo/semantics/openAccess Copying allowed only for non-profit organizations https://serval.unil.ch/disclaimer |