A germline deletion of p14ARF but not CDKN2A in a melanoma-neural system tumour syndrome family

被引:204
作者
Randerson-Moor, JA
Harland, M
Williams, S
Cuthbert-Heavens, D
Sheridan, E
Aveyard, J
Sibley, K
Whitaker, L
Knowles, M
Bishop, JN
Bishop, DT
机构
[1] St James Univ Hosp, Imperial Canc Res Fund, Ctr Clin, Genet Epidemiol Div, Leeds LS9 7TF, W Yorkshire, England
[2] St James Univ Hosp, Imperial Canc Res Fund, Ctr Clin, Genet Mol Lab, Leeds LS9 7TF, W Yorkshire, England
[3] St James Univ Hosp, Imperial Canc Res Fund, Mutat Detect Facil, Leeds LS9 7TF, W Yorkshire, England
[4] St James Univ Hosp, Imperial Canc Res Fund, Ctr Clin, Canc Med Unit, Leeds LS9 7TF, W Yorkshire, England
关键词
D O I
10.1093/hmg/10.1.55
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
The melanoma-astrocytoma syndrome is characterized by a dual predisposition to melanoma and neural system tumours, commonly astrocytoma. Germline deletions of the region on 9p21 containing the CDKN2A and CDKN2B genes and CDKN2A exon 1 beta have been reported in kindreds, implicating contiguous tumour suppressor gene deletion as a cause of this syndrome. We describe a family characterized by multiple melanoma and neural cell tumours segregating with a germline deletion of the p14(ARF)-specific exon 1 beta of the CDKN2A gene. This deletion does not affect the coding or minimal promoter sequences of either the CDKN2A or CDKN2B genes. Our results are consistent with either: (i) loss of p14(ARF) function being the critical abnormality associated with this syndrome, rather than contiguous loss of both the CDKN2A and CDKN2B genes as suggested previously; or (ii) disruption of expression of p16 by mechanisms as yet unknown.
引用
收藏
页码:55 / 62
页数:8
相关论文
共 44 条
[21]  
Laurendeau I, 1999, CLIN CHEM, V45, P982
[22]  
Liu L, 1997, GENE CHROMOSOME CANC, V19, P52, DOI 10.1002/(SICI)1098-2264(199705)19:1<52::AID-GCC8>3.3.CO
[23]  
2-S
[24]  
MAO L, 1995, CANCER RES, V55, P2995
[25]   Incidence of p14ARF gene deletion in high-grade adult and pediatric astrocytomas [J].
Newcomb, EW ;
Alonso, M ;
Sung, T ;
Miller, DC .
HUMAN PATHOLOGY, 2000, 31 (01) :115-119
[26]   Mutation testing in melanoma families: INK4A, CDK4 and INK4D [J].
Newton-Bishop, JA ;
Harland, M ;
Bennett, DC ;
Bataille, V ;
Goldstein, AM ;
Tucker, MA ;
Ponder, BAJ ;
Cuzick, J ;
Selby, P ;
Bishop, DT .
BRITISH JOURNAL OF CANCER, 1999, 80 (1-2) :295-300
[27]  
Ohta M, 1996, INT J CANCER, V65, P762, DOI 10.1002/(SICI)1097-0215(19960315)65:6<762::AID-IJC9>3.3.CO
[28]  
2-B
[29]   AMPLIFICATION OF A GENE ENCODING A P53-ASSOCIATED PROTEIN IN HUMAN SARCOMAS [J].
OLINER, JD ;
KINZLER, KW ;
MELTZER, PS ;
GEORGE, DL ;
VOGELSTEIN, B .
NATURE, 1992, 358 (6381) :80-83
[30]  
Peelen T, 1997, AM J HUM GENET, V61, pA14