The cleavage of microphthalmia-associated transcription factor, MITF, by caspases plays an essential role in melanocyte and melanoma cell apoptosis

被引:53
作者
Larribere, L
Hilmi, C
Khaled, M
Gaggioli, C
Bille, K
Auberger, P
Ortonne, JP
Ballotti, R
Bertolotto, C [1 ]
机构
[1] INSERM, U597, Ligue Natl Canc, Equipe Labellisee 2001, F-06107 Nice, France
[2] INSERM, U526, Ligue Natl Canc, Equipe Labellisee 2003, F-06107 Nice, France
关键词
apoptosis; caspase; melanoma; MITF;
D O I
10.1101/gad.335905
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Microphthalmia-associated transcription factor (MITF) M-form is a melanocyte-specific transcription factor that plays a key role in melanocyte development, survival, and differentiation. Here, we identified MITF as a new substrate of caspases and we characterized the cleavage site after Asp 345 in the C-terminal domain. We show that expression of a noncleavable form of MITF renders melanoma cells resistant to apoptotic stimuli, and we found that the C-terminal fragment generated upon caspase cleavage is endowed with a proapoptotic activity that sensitizes melanoma cells to death signals. The proapoptotic function gained by MITF following its processing by caspases provides a tissue-restricted means to modulate death in melanocyte and melanoma cells.
引用
收藏
页码:1980 / 1985
页数:6
相关论文
共 33 条
[1]   Regulation of tyrosinase gene expression by cAMP in B16 melanoma cells involves two CATGTG motifs surrounding the TATA box: Implication of the microphthalmia gene product [J].
Bertolotto, C ;
Bille, K ;
Ortonne, JP ;
Ballotti, R .
JOURNAL OF CELL BIOLOGY, 1996, 134 (03) :747-755
[2]   Different cis-acting elements are involved in the regulation of TRP1 and TRP2 promoter activities by cyclic AMP:: Pivotal role of M boxes (GTCATGTGCT) and of microphthalmia [J].
Bertolotto, C ;
Buscà, R ;
Abbe, P ;
Bille, K ;
Aberdam, E ;
Ortonne, JP ;
Ballotti, R .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (02) :694-702
[3]   Microphthalmia gene product as a signal transducer in cAMP-induced differentiation of melanocytes [J].
Bertolotto, C ;
Abbe, P ;
Hemesath, TJ ;
Bille, K ;
Fisher, DE ;
Ortonne, JP ;
Ballotti, R .
JOURNAL OF CELL BIOLOGY, 1998, 142 (03) :827-835
[4]   Mitf cooperates with Rb1 and activates p21Cip1 expression to regulate cell cycle progression [J].
Carreira, S ;
Goodall, J ;
Aksan, I ;
La Rocca, SA ;
Galibert, MD ;
Denat, L ;
Larue, L ;
Goding, CR .
NATURE, 2005, 433 (7027) :764-769
[5]   The transmembrane domain of hepatitis C virus E1 glycoprotein induces cell death [J].
Ciccaglione, AR ;
Marcantonio, C ;
Tritarelli, E ;
Equestre, M ;
Magurano, F ;
Costantino, A ;
Nicoletti, L ;
Rapicetta, M .
VIRUS RESEARCH, 2004, 104 (01) :1-9
[6]   Modulation of cell death by Bcl-xL through caspase interaction [J].
Clem, RJ ;
Cheng, EHY ;
Karp, CL ;
Kirsch, DG ;
Ueno, K ;
Takahashi, A ;
Kastan, MB ;
Griffin, DE ;
Earnshaw, WC ;
Veliuona, MA ;
Hardwick, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (02) :554-559
[7]   Critical role of CDK2 for melanoma growth linked to its melanocyte-specific transcriptional regulation by MITF [J].
Du, JY ;
Widlund, HR ;
Horstmann, MA ;
Ramaswamy, S ;
Ross, K ;
Huber, WE ;
Nishimura, EK ;
Golub, TR ;
Fisher, DE .
CANCER CELL, 2004, 6 (06) :565-576
[8]   Many cuts to ruin:: a comprehensive update of caspase substrates [J].
Fischer, U ;
Jänicke, RU ;
Schulze-Osthoff, K .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (01) :76-100
[9]   Microphthalmia-associated transcription factor (MITF) is required but is not sufficient to induce the expression of melanogenic genes [J].
Gaggioli, C ;
Buscà, R ;
Abbe, P ;
Ortonne, JP ;
Ballotti, R .
PIGMENT CELL RESEARCH, 2003, 16 (04) :374-382
[10]  
Giordano A, 1999, J CELL PHYSIOL, V181, P218, DOI 10.1002/(SICI)1097-4652(199911)181:2<218::AID-JCP4>3.0.CO