Transcriptional analysis of the PTEN/MMAC1 pseudogene, ΨPTEN

被引:73
作者
Fujii, GH [1 ]
Morimoto, AM [1 ]
Berson, AE [1 ]
Bolen, JB [1 ]
机构
[1] DNAX Res Inst Mol & Cellular Biol Inc, Dept Cellular Signaling, Palo Alto, CA 94304 USA
关键词
MMAC; PTEN; tumor suppressor; pseudogene;
D O I
10.1038/sj.onc.1202492
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 is a recently characterized tumor suppressor. A pseudogene derived from the human PTEN/MMAC1 phosphatase, Psi PTEN, has been reported. Recent analysis of the pseudogene revealed conflicting results about the expression of Psi PTEN. In this study, we show that the PTEN/MMAC1 pseudogene is actively transcribed in all cells and tissues examined. In some cases, pseudogene transcripts were found to represent as much as 70% of the total PTEN/MMAC1 RNA. As Psi PTEN is transcribed, there is a potential for misinterpretation of PTEN/MMAC1 mutations when RT - PCR techniques are used, as well as potential for a Psi PTEN-encoded translation product, Although we were unable to detect a pseudogene protein product in the cell lines examined, a baculovirus produced GST pseudogene fusion protein exhibited phosphatase activity comparable to wild type. The results of this study, taken together, indicate the potential complication of PTEN/MMAC1 molecular analysis caused by the expression of Psi PTEN.
引用
收藏
页码:1765 / 1769
页数:5
相关论文
共 27 条
[1]   FREQUENCY OF HOMOZYGOUS DELETION AT P16/CDKN2 IN PRIMARY HUMAN TUMORS [J].
CAIRNS, P ;
POLASCIK, TJ ;
EBY, Y ;
TOKINO, K ;
CALIFANO, J ;
MERLO, A ;
MAO, L ;
HERATH, J ;
JENKINS, R ;
WESTRA, W ;
RUTTER, JL ;
BUCKLER, A ;
GABRIELSON, E ;
TOCKMAN, M ;
CHO, KR ;
HEDRICK, L ;
BOVA, GS ;
ISAACS, W ;
KOCH, W ;
SCHWAB, D ;
SIDRANSKY, D .
NATURE GENETICS, 1995, 11 (02) :210-212
[2]  
Cheney IW, 1998, CANCER RES, V58, P2331
[3]  
CHENG JQ, 1994, CANCER RES, V54, P5547
[4]   A highly conserved processed PTEN pseudogene is located on chromosome band 9p21 [J].
Dahia, PLM ;
FitzGerald, MG ;
Zhang, X ;
Marsh, DJ ;
Zheng, ZM ;
Pietsch, T ;
von Deimling, A ;
Haluska, FG ;
Haber, DA ;
Eng, C .
ONCOGENE, 1998, 16 (18) :2403-2406
[5]   Growth suppression of glioma cells by PTEN requires a functional phosphatase catalytic domain [J].
Furnari, FB ;
Lin, H ;
Huang, HJS ;
Cavenee, WK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (23) :12479-12484
[6]   A CELL-CYCLE REGULATOR POTENTIALLY INVOLVED IN GENESIS OF MANY TUMOR TYPES [J].
KAMB, A ;
GRUIS, NA ;
WEAVERFELDHAUS, J ;
LIU, QY ;
HARSHMAN, K ;
TAVTIGIAN, SV ;
STOCKERT, E ;
DAY, RS ;
JOHNSON, BE ;
SKOLNICK, MH .
SCIENCE, 1994, 264 (5157) :436-440
[7]   Alterations of PTEN/MMAC1, a candidate tumor suppressor gene, and its homologue, PTH2, in small cell lung cancer cell lines [J].
Kim, SK ;
Su, LK ;
Oh, Y ;
Kemp, BL ;
Hong, WK ;
Mao, L .
ONCOGENE, 1998, 16 (01) :89-93
[8]  
Li DM, 1997, CANCER RES, V57, P2124
[9]   PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer [J].
Li, J ;
Yen, C ;
Liaw, D ;
Podsypanina, K ;
Bose, S ;
Wang, SI ;
Puc, J ;
Miliaresis, C ;
Rodgers, L ;
McCombie, R ;
Bigner, SH ;
Giovanella, BC ;
Ittmann, M ;
Tycko, B ;
Hibshoosh, H ;
Wigler, MH ;
Parsons, R .
SCIENCE, 1997, 275 (5308) :1943-1947
[10]   Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome [J].
Liaw, D ;
Marsh, DJ ;
Li, J ;
Dahia, PLM ;
Wang, SI ;
Zheng, ZM ;
Bose, S ;
Call, KM ;
Tsou, HC ;
Peacocke, M ;
Eng, C ;
Parsons, R .
NATURE GENETICS, 1997, 16 (01) :64-67