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

被引:140
作者
Rizos, H [1 ]
Puig, S
Badenas, C
Malvehy, J
Darmanian, AP
Jiménez, L
Milà, M
Kefford, RF
机构
[1] Univ Sydney, Westmead Millennium Inst, Westmead Hosp, Westmead Inst Canc Res, Westmead, NSW 2145, Australia
[2] Univ Barcelona, IDIBAPS, Hosp Clin, E-08036 Barcelona, Spain
基金
英国医学研究理事会;
关键词
p14ARF; p16(INK4a); melanoma; germline mutation;
D O I
10.1038/sj.onc.1204728
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 INK4a/ARF locus encodes the cyclin dependent kinase inhibitor, p16(INK4a) and the p53 activator, p14ARF. These two proteins have an independent first exon (exon 1 alpha and exon 1 beta, 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 p16(INK4a), more than 40% of the INK4a/ARF alterations located in exon 2, affect both p16(INK4a) and p14ARF. We now report a 16 base pair exon 1 beta germline insertion specifically altering p14ARF, but not p16(INK4a), 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 1 beta mutation that inactivates p14ARF, and thus implicates a role for this tumour suppressor in melanoma predisposition.
引用
收藏
页码:5543 / 5547
页数:5
相关论文
共 41 条
[1]   Methylation silencing and mutations of the p14ARF and p16INK4a genes in colon cancer [J].
Burri, N ;
Shaw, P ;
Bouzourene, H ;
Sordat, I ;
Sordat, B ;
Gillet, M ;
Schorderet, D ;
Bosman, FT ;
Chaubert, P .
LABORATORY INVESTIGATION, 2001, 81 (02) :217-229
[2]   p16INK4A and p19ARF act in overlapping pathways in cellular immortalization [J].
Carnero, A ;
Hudson, JD ;
Price, CM ;
Beach, DH .
NATURE CELL BIOLOGY, 2000, 2 (03) :148-155
[3]  
Dracopoli NC, 1996, CANCER SURV, V26, P115
[4]   Human ARF binds E2F1 and inhibits its transcriptional activity [J].
Eymin, B ;
Karayan, L ;
Séité, P ;
Brambilla, C ;
Brambilla, E ;
Larsen, CJ ;
Gazzéri, S .
ONCOGENE, 2001, 20 (09) :1033-1041
[5]   Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds [J].
Flores, JF ;
Pollock, PM ;
Walker, GJ ;
Glendening, JM ;
Lin, AHT ;
Palmer, JM ;
Walters, MK ;
Hayward, NK ;
Fountain, JW .
ONCOGENE, 1997, 15 (24) :2999-3005
[6]   Mdm2 association with p53 targets its ubiquitination [J].
Fuchs, SY ;
Adler, V ;
Buschmann, T ;
Wu, XW ;
Ronai, Z .
ONCOGENE, 1998, 17 (19) :2543-2547
[7]   Genomic alterations of the p19ARF encoding exons in T-cell acute lymphoblastic leukemia [J].
Gardie, B ;
Cayuela, JM ;
Martini, S ;
Sigaux, F .
BLOOD, 1998, 91 (03) :1016-1020
[8]   Association of p19ARF with Mdm2 inhibits ubiquitin ligase activity of Mdm2 for tumor suppressor p53 [J].
Honda, R ;
Yasuda, H .
EMBO JOURNAL, 1999, 18 (01) :22-27
[9]   Tumor suppression at the mouse INK4a locus mediated by the alternative reading frame product p19(ARF) [J].
Kamijo, T ;
Zindy, F ;
Roussel, MF ;
Quelle, DE ;
Downing, JR ;
Ashmun, RA ;
Grosveld, G ;
Sherr, CJ .
CELL, 1997, 91 (05) :649-659
[10]  
Kumar R, 1998, GENE CHROMOSOME CANC, V23, P273, DOI 10.1002/(SICI)1098-2264(199811)23:3<273::AID-GCC11>3.0.CO