A melanoma-associated germline mutation in exon 1β inactivates p14ARF

被引:0
|
作者
Helen Rizos
Susana Puig
Cèlia Badenas
Josep Malvehy
Artur P Darmanian
Loli Jiménez
Montserrat Milà
Richard F Kefford
机构
[1] Westmead Institute for Cancer Research,
[2] University of Sydney at Westmead Millennium Institute,undefined
[3] Westmead Hospital,undefined
[4] Hospital Clinic,undefined
[5] IDIBAPS,undefined
[6] Universitat de Barcelona,undefined
来源
Oncogene | 2001年 / 20卷
关键词
p14ARF; p16; melanoma; germline mutation;
D O I
暂无
中图分类号
学科分类号
摘要
The INK4a/ARF locus encodes the cyclin dependent kinase inhibitor, p16INK4a and the p53 activator, p14ARF. These two proteins have an independent first exon (exon 1α and exon 1β, respectively) but share exons 2 and 3 and are translated in different reading frames. Germline mutations in this locus are associated with melanoma susceptibility in 20–40% of multiple case melanoma families. Although most of these mutations specifically inactivate p16INK4a, more than 40% of the INK4a/ARF alterations located in exon 2, affect both p16INK4a and p14ARF. We now report a 16 base pair exon 1β germline insertion specifically altering p14ARF, but not p16INK4a, in an individual with multiple primary melanomas. This mutant p14ARF, 60ins16, was restricted to the cytoplasm, did not stabilize p53 and was unable to arrest the growth of a p53 expressing melanoma cell line. This is the first example of an exon 1β mutation that inactivates p14ARF, and thus implicates a role for this tumour suppressor in melanoma predisposition.
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页码:5543 / 5547
页数:4
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