Duplication of ATR inhibits MyoD, induces aneuploidy and eliminates radiation-induced G1 arrest

被引:72
作者
Smith, L
Liu, SJ
Goodrich, L
Jacobson, D
Degnin, C
Bentley, N
Carr, A
Flaggs, G
Keegan, K
Hoekstra, M
Thayer, MJ
机构
[1] Oregon Hlth & Sci Univ, Vollum Inst, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Med & Mol Genet, Portland, OR 97201 USA
[3] Univ Sussex, MRC, Cell Mutat Unit, Brighton BN1 9RR, E Sussex, England
[4] ICOS Corp, Bothell, WA 98021 USA
关键词
D O I
10.1038/ng0598-39
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Chromosome Sq alterations occur frequently in many types of tumours. In a genetic screen for loci present in rhabdomyosarcomas, we identified an isochromosome 3q [i(3q)], which inhibits muscle differentiation when transferred into myoblasts. The i(3q) inhibits MyoD function, resulting in a non-differentiating phenotype. Furthermore, the i(3q) induces a 'cut' phenotype, abnormal centrosome amplification, aneuploidy and loss of G1 arrest following gamma-irradiation, Testing candidate genes within this region reveals that forced expression of ataxia-telangiectasia and rad3-related (ATR) results in a phenocopy of the i(3q). Thus, genetic alteration of ATR leads to loss of differentiation as well as cell-cycle abnormalities.
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收藏
页码:39 / 46
页数:8
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