Ubiquitylation of Fe65 adaptor protein by neuronal precursor cell expressed developmentally down regulated 4-2 (Nedd4-2) via the WW domain interaction with Fe65.
10.3858/emm.2009.41.8.061
- Author:
Eun Jeoung LEE
1
;
Sunghee HYUN
;
Jaesun CHUN
;
Sung Hwa SHIN
;
Sang Sun KANG
Author Information
1. School of Science Education, Chungbuk National University, Cheongju 361-763, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
APBB2 protein, human;
Nedd4 ubiquitin protein ligases;
protein interaction domains and motifs;
protein interaction mapping;
ubiquitin
- MeSH:
Adaptor Proteins, Signal Transducing/chemistry/genetics/*metabolism;
Cell Line;
*Down-Regulation;
Endosomal Sorting Complexes Required for Transport/genetics/*metabolism;
*Gene Expression Regulation, Developmental;
Humans;
Immunoprecipitation;
Microscopy, Confocal;
Mutation;
Protein Interaction Mapping;
Protein Structure, Tertiary/*physiology;
Transfection;
Ubiquitin-Protein Ligases/genetics/*metabolism;
Ubiquitination
- From:Experimental & Molecular Medicine
2009;41(8):555-568
- CountryRepublic of Korea
- Language:English
-
Abstract:
Fe65 has been characterized as an adaptor protein, originally identified as an expressed sequence tag (EST) corresponding to an mRNA expressed at high levels in the rat brain. It contains one WW domain and two phosphotyrosine interaction/phosphotyrosine binding domains (PID1/PID2). As the neuronal precursor cell expressed developmentally down regulated 4-2 (Nedd4-2) has a putative WW domain binding motif (72PPLP75) in the N-terminal domain, we hypothesized that Fe65 associates with Nedd4-2 through a WW domain interaction, which has the characteristics of E3 ubiquitin-protein ligase. In this paper, we present evidence for the interaction between Fe65 WW domain and Nedd4-2 through its specific motif, using a pull down approach and co-immunoprecipitation. Additionally, the co-localization of Fe65 and Nedd4-2 were observed via confocal microscopy. Co-localization of Fe65 and Nedd4-2 was disrupted by either the mutation of Fe65 WW domain or its putative binding motif of Nedd4-2. When the ubiquitin assay was performed, the interaction of Nedd4-2 (wt) with Fe65 is required for the cell apoptosis and the ubiquitylation of Fe65. We also observed that the ubiquitylation of Fe65 (wt) was augmented depending on Nedd4-2 expression levels, whereas the Fe65 WW domain mutant (W243KP245K) or the Nedd4-2 AL mutant (72PPLP75 was changed to 72APLA75) was under-ubiquitinated significantly. Thus, our observations implicated that the protein-protein interaction between the WW domain of Fe65 and the putative binding motif of Nedd4-2 down-regulates Fe65 protein stability and subcellular localization through its ubiquitylation, to contribute cell apoptosis.
