Identification of DeltaNp63alpha protein interactions by mass spectrometry.
p63, a transcription factor related to the p53 tumor suppressor, plays a key role in epidermal differentiation and limb development. The gene has two distinct promoters that allow the formation of proteins that either contain (TA) or lack (DeltaN) a transactivation domain. DeltaNp63alpha is the most widely expressed isoform, at ... all stages of development and in adult tissues. It supports the regenerative capacity of basal keratinocytes and its upregulation is a hallmark of human squamous carcinomas. To get insight into the complex biology of DeltaNp63alpha, we set out to identify DeltaNp63alpha interacting proteins by co-immunoprecipitation in mammalian cells and mass spectrometry analysis. A total of 49 potential DeltaNp63alpha binding proteins, including several heterogeneous ribonucleoproteins (hnRNPs), were identified. Integration of the proteomic data with a Human Coexpression Network highlighted 5 putative p63 protein interactors whose expression is significantly comodulated with p63: hnRNPA/B, hnRNPK, hnRNPQ, FUS/TLS and Keratin 5. hnRNPA/B was already described as a p63 partner, but the others were novel. Interaction of DeltaNp63alpha with hnRNPQ, hnRNPK and FUS/TLS was confirmed by reciprocal co-immunoprecipitations in human keratinocytes. The finding that DeltaNp63alpha exists in complexes with several RNA-binding proteins lays the premises for the analysis of the role of DeltaNp63alpha in mRNA metabolism and transport.
Mesh Terms:
Cell Line, Tumor, Cluster Analysis, Databases, Protein, Heterogeneous-Nuclear Ribonucleoproteins, Humans, Protein Interaction Mapping, Protein Isoforms, Proteins, RNA-Binding Protein FUS, Tandem Mass Spectrometry, Trans-Activators, Transcription Factors, Tumor Suppressor Proteins
Cell Line, Tumor, Cluster Analysis, Databases, Protein, Heterogeneous-Nuclear Ribonucleoproteins, Humans, Protein Interaction Mapping, Protein Isoforms, Proteins, RNA-Binding Protein FUS, Tandem Mass Spectrometry, Trans-Activators, Transcription Factors, Tumor Suppressor Proteins
J. Proteome Res.
Date: Apr. 05, 2010
PubMed ID: 20085233
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