Cancer predisposition caused by elevated mitotic recombination in Bloom mice

被引:319
作者
Luo, GB
Santoro, IM
McDaniel, LD
Nishijima, I
Mills, M
Youssoufian, H
Vogel, H
Schultz, RA
Bradley, A
机构
[1] Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Univ Texas, SW Med Ctr, McDermott Ctr Human Growth & Dev, Dallas, TX USA
关键词
D O I
10.1038/82548
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Bloom syndrome is a disorder associated with genomic instability that causes affected people to be prone to cancer. Bloom cell lines show increased sister chromatid exchange, yet are proficient in the repair of various DNA lesions. The underlying cause of this disease are mutations in a gene encoding a RECQ DNA helicase. Using embryonic stem cell technology, we have generated viable Bloom mice that are prone to a wide variety of cancers. Cell lines from these mice show elevations in the rates of mitotic recombination. We demonstrate that the increased rate of loss of heterozygosity (LOH) resulting from mitotic recombination in vivo constitutes the underlying mechanism causing tumour susceptibility in these mice.
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收藏
页码:424 / 429
页数:6
相关论文
共 36 条
[1]  
Abuin A, 1996, MOL CELL BIOL, V16, P1851
[2]   Manipulation of the mouse germline in the study of Min-induced neoplasia [J].
Bilger, A ;
Shoemaker, AR ;
Gould, KA ;
Dove, WF .
SEMINARS IN CANCER BIOLOGY, 1996, 7 (05) :249-260
[3]  
Chakraverty RK, 1999, BIOESSAYS, V21, P286
[4]   Stage-specific apoptosis, developmental delay, and embryonic lethality in mice homozygous for a targeted disruption in the murine Bloom's syndrome gene [J].
Chester, N ;
Kuo, F ;
Kozak, C ;
O'Hara, CD ;
Leder, P .
GENES & DEVELOPMENT, 1998, 12 (21) :3382-3393
[5]  
COLLET B, 1995, INTERNET WORLD, V6, P8
[6]   Fission yeast rad12+ regulates cell cycle checkpoint control and is homologous to the Bloom's syndrome disease gene [J].
Davey, S ;
Han, CS ;
Ramer, SA ;
Klassen, JC ;
Jacobson, A ;
Eisenberger, A ;
Hopkins, KM ;
Lieberman, HB ;
Freyer, GA .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (05) :2721-2728
[7]   GENETIC IDENTIFICATION OF MOM-1, A MAJOR MODIFIER LOCUS AFFECTING MIN-INDUCED INTESTINAL NEOPLASIA IN THE MOUSE [J].
DIETRICH, WF ;
LANDER, ES ;
SMITH, JS ;
MOSER, AR ;
GOULD, KA ;
LUONGO, C ;
BORENSTEIN, N ;
DOVE, W .
CELL, 1993, 75 (04) :631-639
[8]  
Dong LW, 1996, J MOL RECOGNIT, V9, P383, DOI 10.1002/(SICI)1099-1352(199634/12)9:5/6<383::AID-JMR269>3.0.CO
[9]  
2-Z
[10]   THE BLOOMS-SYNDROME GENE-PRODUCT IS HOMOLOGOUS TO RECQ HELICASES [J].
ELLIS, NA ;
GRODEN, J ;
YE, TZ ;
STRAUGHEN, J ;
LENNON, DJ ;
CIOCCI, S ;
PROYTCHEVA, M ;
GERMAN, J .
CELL, 1995, 83 (04) :655-666