A highly conserved processed PTEN pseudogene is located on chromosome band 9p21

被引:81
|
作者
Dahia, PLM
FitzGerald, MG
Zhang, X
Marsh, DJ
Zheng, ZM
Pietsch, T
von Deimling, A
Haluska, FG
Haber, DA
Eng, C
机构
[1] Dana Farber Canc Inst, Charles A Dana Human Canc Genet Unit, Dept Adult Oncol, Translat Res Lab, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Program Populat Sci, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[4] Massachusetts Gen Hosp, Ctr Canc, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Ctr Canc, Charlestown, MA USA
[6] Univ Bonn, Med Ctr, Dept Neuropathol, D-53105 Bonn, Germany
[7] Univ Cambridge, Canc Res Campaign, Human Canc Genet Res Grp, Cambridge CB2 2QQ, England
关键词
MMAC1; TEP1; 9p; Cowden; pseudogene;
D O I
10.1038/sj.onc.1201762
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PTEN/MMAC1/TEP1, encoding a dual-specificity phosphatase, is a tumor suppressor gene which has recently been cloned and mapped to chromosome 10q23.3. We have shown that germline mutations of PTEN are present in individuals with two hamartoma syndromes: Cowden Syndrome, associated with a predisposition to breast and thyroid cancers, and Bannayan-Zonana syndrome. Somatic mutations of PTEN have been reported in a variety of human cancer cell lines, suggesting a potential role for this gene in the pathogenesis of human malignancies. We report the identification of a highly conserved PTEN processed pseudogene, psi PTEN, which shares over 98% homology with the coding region of functional PTEN, and its localisation to chromosome 9p21. The high sequence homology of psi PTEN with the PTEN transcript may potentially lead to misinterpretation when performing mutation analyses based on cDNA templates. Caution should be exerted when using such screening approaches.
引用
收藏
页码:2403 / 2406
页数:4
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