TBC1D3, a hominoid oncoprotein, is encoded by a cluster of paralogues located on chromosome 17q12

被引:48
作者
Hodzic, Didier [1 ]
Kong, Chen [1 ]
Wainszelbaum, Marisa J. [1 ]
Charron, Audra J. [1 ]
Su, Xiong [1 ]
Stahl, Philip D. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
TBC1D3; PRC17; RAB5A; endocytosis; oncogene; 17q12;
D O I
10.1016/j.ygeno.2006.05.009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
TBC1D3 is a member of the TBC1 domain family of proteins that stimulates the intrinsic GTPase activity of RAB5A, an essential actor in early endosome trafficking. Oncogenic properties of TBC1D3 have been demonstrated previously both in vitro and in mouse models. Although the oncogenic mechanism of TBC1D3 has yet to be elucidated, the TBC1D3 locus (chromosome 17q12) is amplified in 15% of primary prostate tumors. Here, we describe eight highly related TBC1D3 paralogues located within that genomic region, potentially encoding six variant TBC1D3 proteins. We found that human tissues display specific transcription patterns of these paralogues. Furthermore, that pattern was altered in several primary prostate tumors in comparison to healthy prostate tissues. Potential TBC1D3 oncogenic mechanisms are discussed in light of these results. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:731 / 736
页数:6
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