Previous gene microarray studies have shown that expression of 14-3-3θ is significantly decreased in an α-synuclein transgenic mouse model. In this study, we tested whether α-synuclein can regulate 14-3-3θ transcription. We demonstrate that the 14-3-3θ mRNA level is decreased in SH-SY5Y cells overexpressing α-synuclein. Luciferase activity under the control of the 14-3-3θ promoter is reduced both in stable SH-SY5Y cells constitutively overexpressing α-synuclein and in doxycycline-inducible SH-SY5Y cells upon α-synuclein induction, suggesting that the regulation of 14-3-3θ by α-synuclein occurs at the transcriptional level. Knockdown of α-synuclein by RNA interference does not increase the 14-3-3θ mRNA level. These findings suggest that α-synuclein represses 14-3-3θ transcription under pathologic conditions, but that regulation of 14-3-3θ expression is not a function of endogenous α-synuclein at baseline.
α-Synuclein overexpression represses 14-3-3θ transcription.
α-突触核蛋白过表达抑制14-3-3α转录
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作者:Ding Huiping, Fineberg Naomi S, Gray Michelle, Yacoubian Talene A
| 期刊: | Journal of Molecular Neuroscience | 影响因子: | 2.700 |
| 时间: | 2013 | 起止号: | 2013 Nov;51(3):1000-9 |
| doi: | 10.1007/s12031-013-0086-5 | 研究方向: | 其它 |
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