Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B

被引:481
作者
Hanks, S
Coleman, K
Reid, S
Plaja, A
Firth, H
FitzPatrick, D
Kidd, A
Méhes, K
Nash, R
Robin, N
Shannon, N
Tolmie, J
Swansbury, J
Irrthum, A
Douglas, J
Rahman, N [1 ]
机构
[1] Inst Canc Res, Sect Canc Genet, Surrey, England
[2] Hosp Materno Infantil Vall dHebron, Unitat Genet, Barcelona, Spain
[3] Addenbrookes Hosp, Dept Med Genet, Cambridge, England
[4] Wellington Hosp, Cent Reg Genet Serv, Wellington, New Zealand
[5] MRC, Human Genet Unit, Edinburgh, Midlothian, Scotland
[6] Univ Pecs, Dept Med Genet & Child Dev, Pecs, Hungary
[7] Case Western Reserve Univ, Dept Human Genet, Cleveland, OH 44106 USA
[8] Birmingham Womens Hosp, W Midland Reg Genet Serv, Birmingham, W Midlands, England
[9] Inst Med Genet, Glasgow, Lanark, Scotland
[10] Inst Canc Res, Sect Haematooncol, Surrey, England
关键词
D O I
10.1038/ng1449
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Mosaic variegated aneuploidy is a rare recessive condition characterized by growth retardation, microcephaly, childhood cancer and constitutional mosaicism for chromosomal gains and losses. In five families with mosaic variegated aneuploidy, including two with embryonal rhabdomyosarcoma, we identified truncating and missense mutations of BUB1B, which encodes BUBR1, a key protein in the mitotic spindle checkpoint. These data are the first to relate germline mutations in a spindle checkpoint gene with a human disorder and strongly support a causal link between aneuploidy and cancer development.
引用
收藏
页码:1159 / 1161
页数:3
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