Many ribosomal protein genes are cancer genes in zebrafish

被引:345
作者
Amsterdam, A
Sadler, KC
Lai, K
Farrington, S
Bronson, RT
Lees, JA
Hopkins, N [1 ]
机构
[1] MIT, Canc Res Ctr, Cambridge, MA 02139 USA
[2] Tufts Univ, Sch Vet Med, Dept Pathol, Boston, MA 02111 USA
关键词
D O I
10.1371/journal.pbio.0020139
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
We have generated several hundred lines of zebrafish (Danio rerio), each heterozygous for a recessive embryonic lethal mutation. Since many tumor suppressor genes are recessive lethals, we screened our colony for lines that display early mortality and/or gross evidence of tumors. We identified 12 lines with elevated cancer incidence. Fish from these lines develop malignant peripheral nerve sheath tumors, and in some cases also other tumor types, with moderate to very high frequencies. Surprisingly, 11 of the 12 lines were each heterozygous for a mutation in a different ribosomal protein (RP) gene, while one line was heterozygous for a mutation in a zebrafish paralog of the human and mouse tumor suppressor gene, neurofibromatosis type 2. Our findings suggest that many RP genes may act as haploinsufficient tumor suppressors in fish. Many RP genes might also be cancer genes in humans, where their role in tumorigenesis could easily have escaped detection up to now.
引用
收藏
页码:690 / 698
页数:9
相关论文
共 43 条
[1]   Zebrafish as a cancer model system [J].
Amatruda, JF ;
Shepard, JL ;
Stern, HM ;
Zon, LI .
CANCER CELL, 2002, 1 (03) :229-231
[2]   A large-scale insertional mutagenesis screen in zebrafish [J].
Amsterdam, A ;
Burgess, S ;
Golling, G ;
Chen, WB ;
Sun, ZX ;
Townsend, K ;
Farrington, S ;
Haldi, M ;
Hopkins, N .
GENES & DEVELOPMENT, 1999, 13 (20) :2713-2724
[3]   Point mutation in essential genes with loss or mutation of the second allele: Relevance to the retention of tumor-specific antigens [J].
Beck-Engeser, GB ;
Monach, PA ;
Mumberg, D ;
Yang, F ;
Wanderling, S ;
Schreiber, K ;
Espinosa, R ;
Le Beau, MM ;
Meredith, SC ;
Schreiber, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (03) :285-299
[4]   Ethylnitrosourea induces neoplasia in zebrafish (Danio rerio) [J].
Beckwith, LG ;
Moore, JL ;
Tsao-Wu, GS ;
Harshbarger, JC ;
Cheng, KC .
LABORATORY INVESTIGATION, 2000, 80 (03) :379-385
[5]   A HUMAN CELLULAR SEQUENCE IMPLICATED IN TRK ONCOGENE ACTIVATION IS DNA DAMAGE INDUCIBLE [J].
BENISHAI, R ;
SCHARF, R ;
SHARON, R ;
KAPTEN, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) :6039-6043
[6]  
Chen F W, 1999, Int Rev Immunol, V18, P429, DOI 10.3109/08830189909088492
[7]   Differential gene expression in apoptosis: Identification of ribosomal protein 23K, a cell proliferation inhibitor [J].
Chen, FW ;
Davies, JP ;
Ioannou, YA .
MOLECULAR GENETICS AND METABOLISM, 1998, 64 (04) :271-282
[8]   Mouse models of tumor development in neurofibromatosis type 1 [J].
Cichowski, K ;
Shih, TS ;
Schmitt, E ;
Santiago, S ;
Reilly, K ;
McLaughlin, ME ;
Bronson, RT ;
Jacks, T .
SCIENCE, 1999, 286 (5447) :2172-2176
[9]   MICE DEFICIENT FOR P53 ARE DEVELOPMENTALLY NORMAL BUT SUSCEPTIBLE TO SPONTANEOUS TUMORS [J].
DONEHOWER, LA ;
HARVEY, M ;
SLAGLE, BL ;
MCARTHUR, MJ ;
MONTGOMERY, CA ;
BUTEL, JS ;
BRADLEY, A .
NATURE, 1992, 356 (6366) :215-221
[10]   The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia [J].
Draptchinskaia, N ;
Gustavsson, P ;
Andersson, B ;
Pettersson, M ;
Willig, TN ;
Dianzani, I ;
Ball, S ;
Tchernia, G ;
Klar, J ;
Matsson, H ;
Tentler, D ;
Mohandas, N ;
Carlsson, B ;
Dahl, N .
NATURE GENETICS, 1999, 21 (02) :169-175