Kaiso-deficient mice show resistance to intestinal cancer

被引:127
作者
Prokhortchouk, A
Sansom, O
Selfridge, J
Caballero, IM
Salozhin, S
Aithozhina, D
Cerchietti, L
Meng, FG
Augenlicht, LH
Mariadason, JM
Hendrich, B
Melnick, A
Prokhortchouk, E
Clarke, A
Bird, A
机构
[1] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[2] Univ Cardiff Wales, Cardiff Sch Biosci, Cardiff, Wales
[3] Russian Acad Sci, Ctr Bioengn, Moscow, Russia
[4] Yeshiva Univ Albert Einstein Coll Med, Dept Dev & Mol Biol & Med Oncol, Bronx, NY 10461 USA
[5] Univ Edinburgh, Inst Stem Cell Res, Edinburgh EH9 3JQ, Midlothian, Scotland
[6] Montefiore Med Ctr, Albert Einstein Canc Ctr, Bronx, NY 10467 USA
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1128/MCB.26.1.199-208.2006
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
Kaiso is a BTB domain protein that associates with the signaling molecule p120-catenin and binds to the methylated sequence mCGmCG or the nonmethylated sequence CTGCNA to modulate transcription. In Xenopus laevis, xKaiso deficiency leads to embryonic death accompanied by premature gene activation in blastulae and upregulation of the xWnt11 gene. Kaiso has also been proposed to play an essential role in mammalian synapse-specific transcription. We disrupted the Kaiso gene in mice to assess its role in mammalian development. Kaiso-null mice were viable and fertile, with no detectable abnormalities of development or gene expression. However, when crossed with tumor-susceptible Apc(Min/+) mice, Kaiso-null mice showed a delayed onset of intestinal tumorigenesis. Kaiso was found to be upregulated in murine intestinal tumors and is expressed in human colon cancers. Our data suggest that Kaiso plays a role in intestinal cancer and may therefore represent a potential target for therapeutic intervention.
引用
收藏
页码:199 / 208
页数:10
相关论文
共 54 条
[1]   Regulation of Rho GTPases by p120-catenin [J].
Anastasiadis, PZ ;
Reynolds, AB .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (05) :604-610
[2]   HIGH-LEVELS OF DENOVO METHYLATION AND ALTERED CHROMATIN STRUCTURE AT CPG ISLANDS IN CELL-LINES [J].
ANTEQUERA, F ;
BOYES, J ;
BIRD, A .
CELL, 1990, 62 (03) :503-514
[3]   Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2 [J].
Chen, WG ;
Chang, Q ;
Lin, YX ;
Meissner, A ;
West, AE ;
Griffith, EC ;
Jaenisch, R ;
Greenberg, ME .
SCIENCE, 2003, 302 (5646) :885-889
[4]   Niche-independent symmetrical self-renewal of a mammalian tissue stem cell [J].
Conti, L ;
Pollard, SM ;
Gorba, T ;
Reitano, E ;
Toselli, M ;
Biella, G ;
Sun, YR ;
Sanzone, S ;
Ying, QL ;
Cattaneo, E ;
Smith, A .
PLOS BIOLOGY, 2005, 3 (09) :1594-1606
[5]   The p120ctn-binding partner Kaiso is a bi-modal DNA-binding protein that recognizes both a sequence-specific consensus and methylated CpG dinucleotides [J].
Daniel, JM ;
Spring, CM ;
Crawford, HC ;
Reynolds, AB ;
Baig, A .
NUCLEIC ACIDS RESEARCH, 2002, 30 (13) :2911-2919
[6]  
Daniel JM, 1999, MOL CELL BIOL, V19, P3614
[7]  
Eads CA, 2002, CANCER RES, V62, P1296
[8]   Wnt signaling in the intestinal epithelium: from endoderm to cancer [J].
Gregorieff, A ;
Clevers, H .
GENES & DEVELOPMENT, 2005, 19 (08) :877-890
[9]   MODULATION OF MTS1 EXPRESSION IN MOUSE AND HUMAN NORMAL AND TUMOR-CELLS [J].
GRIGORIAN, M ;
TULCHINSKY, E ;
BURRONE, O ;
TARABYKINA, S ;
GEORGIEV, G ;
LUKANIDIN, E .
ELECTROPHORESIS, 1994, 15 (3-4) :463-468
[10]   Identification and characterization of a family of mammalian methyl-CpG binding proteins [J].
Hendrich, B ;
Bird, A .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6538-6547