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Focused Review ARTICLE

KF-1 ubiquitin ligase: an anxiety suppressor

1
Department of Biochemistry and Molecular Genetics, Research Institute for Neurological Diseases and Geriatrics, Kyoto Prefectural University of Medicine, Japan
2
Department of Biophysics, Graduate School of Science, Kyoto University, Japan
3
Institute for Comprehensive Medical Science, Fujita Health University, Japan
4
Frontier Technology Center, Kyoto University Graduate School of Medicine, Japan
5
Japan Science and Technology Agency, BIRD & CREST, Japan
Anxiety is an instinct that may have developed to promote adaptive survival by evading unnecessary danger. However, excessive anxiety is disruptive and can be a basic disorder of other psychiatric diseases such as depression. The KF-1, a ubiquitin ligase located on the endoplasmic reticulum (ER), may prevent excessive anxiety; kf-1−/− mice exhibit selectively elevated anxiety-like behavior against light or heights. It is surmised that KF-1 degrades some target proteins, responsible for promoting anxiety, through the ER-associated degradation pathway, similar to Parkin in Parkinson’s disease (PD). Parkin, another ER-ubiquitin ligase, prevents the degeneration of dopaminergic neurons by degrading the target proteins responsible for PD. Molecular phylogenetic studies have revealed that the prototype of kf-1 appeared in the very early phase of animal evolution but was lost, unlike parkin, in the lineage leading up to Drosophila. Therefore, kf-1−/− mice may be a powerful tool for elucidating the molecular mechanisms involved in emotional regulation, and for screening novel anxiolytic/antidepressant compounds.
Keywords:
depression, ERAD pathway, Parkinson’s disease, Alzheimer’s disease, animal evolution
Citation:
Hashimoto-Gotoh T, Iwabe N, Tsujimura A, Takao K and Miyakawa T (2009). KF-1 ubiquitin ligase: an anxiety suppressor. Front. Neurosci. 3:1. doi: 10.3389/neuro.01.004.2009
Received:
29 January 2009;
 Paper pending published:
17 February 2009;
Accepted:
27 February 2009;
 Published online:
01 May 2009.

Edited by:

Carmen Sandi, Ecole Polytechnique Fédérale de Lausanne, Switzerland

Reviewed by:

Valerie J. Bolivar, Wadsworth Center, NYSDOH, USA
Andrew Holmes, National Institute on Alcohol Abuse and Alcoholism, NIH, USA
Copyright:
© 2009 Hashimoto-Gotoh, Iwabe, Tsujimura, Takao and Miyakawa. This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
*Correspondence:
Tamotsu Hashimoto-Gotoh, Department of Biochemistry and Molecular Genetics, Research Institute for Neurological Diseases and Geriatrics, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, Japan. e-mail: thg@koto.kpu-m.ac.jp

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