4.7 Article

TRIM9, a novel brain-specific E3 ubiquitin ligase, is repressed in the brain of Parkinson's disease and dementia with Lewy bodies

期刊

NEUROBIOLOGY OF DISEASE
卷 38, 期 2, 页码 210-218

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2010.01.007

关键词

alpha-Synuclein; Dementia with Lewy bodies; Parkinson's disease; Tripartite motif protein 9 (TRIM9); Ubiquitin

资金

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan
  2. Grant for Hirosaki University Institutional Research
  3. Grant-in-Aid for Studies on the Development of Diagnostic Technique and Therapies for Lewy Body Disease
  4. Ministry of Health, Labour and Welfare, Japan
  5. National Institutes of Health [R01AG024497]
  6. Grants-in-Aid for Scientific Research [20300123] Funding Source: KAKEN

向作者/读者索取更多资源

TRIM family proteins are involved in a broad range of biological processes, and their alteration results in many diverse pathological conditions found in genetic diseases, viral infections, and cancers. However, the spatial and temporal expression and function of TRIM9, one of TRIM family proteins, remain obscure. Our results here showed that TRIM9 protein is mainly expressed in the cerebral cortex, and functions as an E3 ubiquitin ligase collaborating with an E2 ubiquitin conjugating enzyme UbcH5b. Immunohistochemical examination revealed that TRIM9 is localized to the neurons in the normal mouse and human brain and that TRIM9 immunoreactivity is severely decreased in the affected brain areas in Parkinson's disease and dementia with Lewy bodies. This repressed level of TRIM9 protein was supported by immunoblotting analysis. Intriguingly, cortical and brainstem-type Lewy bodies were immunopositive for TRIM9. These results suggest that TRIM9 plays an important role in the regulation of neuronal functions and participates in pathological process of Lewy body disease through its ligase activity. (C) 2010 Elsevier Inc. All rights reserved.

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