α-Synuclein forms a complex with transcription factor Elk-1

Abstract

α-Synuclein has been identified as a component of Lewy bodies in Parkinson's disease and diffuse Lewy body disease, and glial cytoplasmic inclusions (GCls) in multiple system atrophy (MSA). To explore the role of α-synuclein in the pathogenesis, we searched for molecules interacting with α-synuclein and discovered that GCls are stained by anti-Elk-1 antibody. To seek the role of Elk-1 in synucleinopathies, we cotransfected α-synuclein and Elk-1 to cultured cells, and found small granular structure complexes where the two molecules colocalized. Moreover, α-synuclein and Elk-1 were co-immunoprecipitated from the cell lysates. For formation of the complex, the presence of both ETS and B-box domains of Elk-1 was required. Although there was no evidence of direct binding between α-synuclein and Elk-1, we discovered that α-synuclein and Elk-1 both bind to ERK-2, a MAP kinase. The effect of α-synuclein on the MAP kinase pathway was assessed using the Pathdetect system, which showed prominent attenuation of Elk-1 phosphorylation with α-synuclein, and especially A53T mutant. Our results suggest that α-synuclein reacts with the MAP kinase pathway, which might cause dysfunction of neurons and oligodendrocytes and lead to neurodegeneration in Parkinson's disease and MSA.