The adaptor protein DCAF7 mediates the interaction of the adenovirus E1A oncoprotein with the protein kinases DYRK1A and HIPK2

• Published in: Scientific reports 2016-06, Vol.6 (1), p.28241, Article 28241
• Main Authors: Glenewinkel, Florian, Cohen, Michael J., King, Cason R., Kaspar, Sophie, Bamberg-Lemper, Simone, Mymryk, Joe S., Becker, Walter
• Format: Article
• Language: English
• Subjects: 631/80/86; 692/45; Adaptor Proteins, Signal Transducing - physiology; Adenovirus E1A Proteins - chemistry; Adenovirus E1A Proteins - metabolism; Adenoviruses; Amino acids; Binding Sites; Carrier Proteins - chemistry; Carrier Proteins - metabolism; Cell cycle; Cooperation; Dictyostelium - metabolism; Dyrk Kinases; HeLa Cells; Humanities and Social Sciences; Humans; Insects; Kinases; Mold; multidisciplinary; Phosphorylation; Protein Binding; Protein Conformation; Protein Serine-Threonine Kinases - chemistry; Protein Serine-Threonine Kinases - metabolism; Protein-Tyrosine Kinases - chemistry; Protein-Tyrosine Kinases - metabolism; Proteins; Science; Subcellular Fractions - metabolism
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep28241

DYRK1A is a constitutively active protein kinase that has a critical role in growth and development which functions by regulating cell proliferation, differentiation and survival. DCAF7 (also termed WDR68 or HAN11) is a cellular binding partner of DYRK1A and also regulates signalling by the protein kinase HIPK2. DCAF7 is an evolutionarily conserved protein with a single WD40 repeat domain and has no catalytic activity. We have defined a DCAF7 binding motif of 12 amino acids in the N-terminal domain of class 1 DYRKs that is functionally conserved in DYRK1 orthologs from Xenopus , Danio rerio and the slime mold Dictyostelium discoideum. A similar sequence was essential for DCAF7 binding to HIPK2, whereas the closely related HIPK1 family member did not bind DCAF7. Immunoprecipitation and pulldown experiments identified DCAF7 as an adaptor for the association of the adenovirus E1A protein with DYRK1A and HIPK2. Furthermore, DCAF7 was required for the hyperphosphorylation of E1A in DYRK1A or HIPK2 overexpressing cells. Our results characterize DCAF7 as a substrate recruiting subunit of DYRK1A and HIPK2 and suggest that it is required for the negative effect of DYRK1A on E1A-induced oncogenic transformation.