Mutations in the INK4a/ARF melanoma susceptibility locus functionally impair p14ARF

被引:90
作者
Rizos, H [1 ]
Darmanian, AP [1 ]
Holland, EA [1 ]
Mann, GJ [1 ]
Kefford, RF [1 ]
机构
[1] Univ Sydney, Westmead Hosp, Westmead Inst Canc Res, Westmead Millennium Inst, Westmead, NSW 2145, Australia
关键词
D O I
10.1074/jbc.M105299200
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 two cell cycle regulatory proteins, the cy clin-dependent kinase inhibitor, p16(INK4a), and the p53 activator, p14(ARF). Germline mutations in this locus are associated with melanoma susceptibility in 20-40% of multiple case melanoma families. Many of these mutations specifically impair p16(INK4a), whereas mutations uniquely targeting p14(ARF) are rare. Nevertheless, the importance of p14(ARF) has not been excluded because more than 40% of INK4a/ARF alterations affect p16(INK4a) and p14(ARF). We now report that p14(ARF) is functionally impaired in melanoma kindreds carrying INK4a/ARF mutations. Of the seven INK4a/ARF mutations tested, three altered the subcellular distribution of p14(ARF) and diminished the ability of p14(ARF) to activate the p53 pathway. This work establishes the importance of p14(ARF) in melanoma predisposition.
引用
收藏
页码:41424 / 41434
页数:11
相关论文
共 70 条
[1]   MUTATION AND EXPRESSION OF THE P53 GENE IN HUMAN-MALIGNANT MELANOMA [J].
ALBINO, AP ;
VIDAL, MJ ;
MCNUTT, NS ;
SHEA, CR ;
PRIETO, VG ;
NANUS, DM ;
PALMER, JM ;
HAYWARD, NK .
MELANOMA RESEARCH, 1994, 4 (01) :35-45
[2]  
Bartkova J, 1996, CANCER RES, V56, P5475
[3]   p14ARF links the tumour suppressors RB and p53 [J].
Bates, S ;
Phillips, AC ;
Clark, PA ;
Stott, F ;
Peters, G ;
Ludwig, RL ;
Vousden, KH .
NATURE, 1998, 395 (6698) :124-125
[4]   Tumor suppressor p16INK4A:: Determination of solution structure and analyses of its interaction with cyclin-dependent kinase 4 [J].
Byeon, IJL ;
Li, JN ;
Ericson, K ;
Selby, TL ;
Tevelev, A ;
Kim, HJ ;
O'Maille, P ;
Tsai, MD .
MOLECULAR CELL, 1998, 1 (03) :421-431
[5]   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
[6]   Inhibition of v-Abl transformation by p53 and p19ARF [J].
Cong, F ;
Zou, XM ;
Hinrichs, K ;
Calame, K ;
Goff, SP .
ONCOGENE, 1999, 18 (54) :7731-7739
[7]   E1A signaling to p53 involves the p19ARF tumor suppressor [J].
de Stanchina, E ;
McCurrach, ME ;
Zindy, F ;
Shieh, SY ;
Ferbeyre, G ;
Samuelson, AV ;
Prives, C ;
Roussel, MF ;
Sherr, CJ ;
Lowe, SW .
GENES & DEVELOPMENT, 1998, 12 (15) :2434-2442
[8]   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
[9]   CDKN2a/p16INK4a mutations and lack of 0p19ARF involvement in familial melanoma kindreds [J].
Fargnoli, MC ;
Chimenti, S ;
Keller, G ;
Soyer, HP ;
Dal Pozzo, V ;
Höfler, H ;
Peris, K .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1998, 111 (06) :1202-1206
[10]   Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: Analysis of a clinic-based population [J].
FitzGerald, MG ;
Harkin, DP ;
SilvaArrieta, S ;
MacDonald, DJ ;
Lucchina, LC ;
Unsal, H ;
ONeill, E ;
Koh, J ;
Finkelstein, DM ;
Isselbacher, KJ ;
Sober, AJ ;
Haber, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (16) :8541-8545