IMR Press / FBS / Volume 4 / Issue 1 / DOI: 10.2741/s271

Frontiers in Bioscience-Scholar (FBS) is published by IMR Press from Volume 13 Issue 1 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Review

The TRE17/USP6 Oncogene: a riddle wrapped in a mystery inside an enigma

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1 Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN
2 Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, Philadelphia, PA

*Author to whom correspondence should be addressed.

 

Front. Biosci. (Schol Ed) 2012, 4(1), 321–334; https://doi.org/10.2741/s271
Published: 1 January 2012
Abstract

De-ubiquitinating enzymes (DUBs) play critical roles in diverse cellular processes, including intracellular trafficking, protein turnover, inflammatory signaling, and cell transformation. The first DUB to be identified as an oncogene was TRE17/Ubiquitin-specific protease 6 (USP6)/Tre-2. In addition to encoding a USP, TRE17 also contains a TBC (Tre-2/Bub2/Cdc16) domain implicated in GTPase regulation and trafficking. Though first described almost two decades ago, remarkably little has been elucidated regarding TRE17’s molecular and cellular functions. However, recent work has implicated TRE17 as a key etiological factor in aneurysmal bone cyst (ABC), a locally recurrent pediatric bone tumor, and identified potential pathways through which it acts. In this review, we discuss the most up-to-date findings on the molecular functions of TRE17, the role of its USP and TBC domains, and potential models for how it contributes to transformation and ABC pathogenesis.

Keywords
TRE17/USP6
de-ubiquitinating enzyme
ubiquitin-specific protease
aneurysmal bone cyst
TBC domain
Arf6
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