Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2049577 | FEBS Letters | 2007 | 7 Pages |
Abstract
In Lewy body diseases and multiple system atrophy, α-synuclein is hyperphosphorylated at Ser129, suggesting a role in pathogenesis. Here, we report purification of the protein kinase in rat brain that phosphorylates Ser129 and its identification as casein kinase-2 (CK2). We show that most of the activity can be inhibited by heparin, an inhibitor of CK2. Phosphorylated Ser129 was detected in primary cultured neurons and inhibited by CK2 inhibitors. In some cases of Lewy body disease, CK2-like immunoreactivity was recovered in the sarkosyl-insoluble fraction, which was enriched in phosphorylated α-synuclein. Taken together, these findings suggest that CK2 may be involved in the hyperphosphorylation of α-synuclein in α-synucleinopathies.
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Authors
Aasami Ishii, Takashi Nonaka, Sayuri Taniguchi, Taro Saito, Tetsuaki Arai, David Mann, Takeshi Iwatsubo, Shin-ichi Hisanaga, Michel Goedert, Masato Hasegawa,