Differential regulation of c-Jun-dependent transcription by SUMO-specific proteases

被引:52
作者
Cheng, JK
Perkins, ND
Yeh, ETH
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Cardiol, Houston, TX 77030 USA
[2] Univ Texas, Houston Hlth Sci Ctr, Ctr Cardiovasc Dis, Brown Fdn Inst Mol Med Prevent Human Dis, Houston, TX 77030 USA
[3] Univ Dundee, Sch Life Sci, Div Gene Regulat & Express, Dundee DD1 5EH, Scotland
关键词
D O I
10.1074/jbc.M412185200
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
c-Jun is a transcription factor that plays an important role in regulating cell growth, apoptosis, differentiation, and transformation. The transcriptional activity of c-Jun can be regulated by both phosphorylation and sumoylation. It has also been shown that c-Jun transcription can be regulated by SuPr-1, an alternatively spliced form of SUMO-specific protease 2 (SENP2). However, the ability of SuPr-1 to enhance c-Jun transcription is dependent on promyelocytic leukemia but is independent of the desumoylation activity of SuPr-1. Here, we show that SUMO-specific protease 1 (SENP1) also markedly enhances the transcription activity of c-Jun. The action of SENP1 on c-Jun transcription is independent of the sumoylation and phosphorylation status of c-Jun but is critically dependent on the desumoylation activity of SENP1. We further show that p300 is essential for SENP1 to enhance c-Jun-dependent transcription because SENP1 can desumoylate the CRD1 domain of p300, thereby releasing the cis-repression of CRD1 on p300. Thus, two SUMO-specific proteases regulate c-Jun-dependent transcription through entirely different mechanisms.
引用
收藏
页码:14492 / 14498
页数:7
相关论文
共 70 条
[1]   Histone acetyltransferase activity of CBP is controlled by cycle-dependent kinases and oncoprotein E1A [J].
Ait-Si-Ali, S ;
Ramirez, S ;
Barre, FX ;
Dkhissi, F ;
Magnaghi-Jaulin, L ;
Girault, JA ;
Robin, P ;
Knibiehler, M ;
Pritchard, LL ;
Ducommun, B ;
Trouche, D ;
Harel-Bellan, A .
NATURE, 1998, 396 (6707) :184-186
[2]   Activation of the cyclin D1 gene by the EPA-associated protein p300 through AP-1 inhibits cellular apoptosis [J].
Albanese, C ;
D'Amico, M ;
Reutens, AT ;
Fu, MF ;
Watanabe, G ;
Lee, RJ ;
Kitsis, RN ;
Henglein, B ;
Avantaggiati, M ;
Somasundaram, K ;
Thimmapaya, B ;
Pestell, RG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (48) :34186-34195
[3]   THE JUN PROTO-ONCOGENE IS POSITIVELY AUTOREGULATED BY ITS PRODUCT, JUN/AP-1 [J].
ANGEL, P ;
HATTORI, K ;
SMEAL, T ;
KARIN, M .
CELL, 1988, 55 (05) :875-885
[4]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[5]  
[Anonymous], BIOCH BIOPHYS ACTA
[6]   ACTIVATION OF CAMP AND MITOGEN RESPONSIVE GENES RELIES ON A COMMON NUCLEAR FACTOR [J].
ARIAS, J ;
ALBERTS, AS ;
BRINDLE, P ;
CLARET, FX ;
SMEAL, T ;
KARIN, M ;
FERAMISCO, J ;
MONTMINY, M .
NATURE, 1994, 370 (6486) :226-229
[7]   The SUMO-1 isopeptidase Smt4 is linked to centromeric cohesion through SUMO-1 modification of DNA Topoisomerase II [J].
Bachant, J ;
Alcasabas, A ;
Blat, Y ;
Kleckner, N ;
Elledge, SJ .
MOLECULAR CELL, 2002, 9 (06) :1169-1182
[8]  
Bannister AJ, 1995, ONCOGENE, V11, P2509
[9]   Oncogenic transformation by ras and fos is mediated by c-Jun N-terminal phosphorylation [J].
Behrens, A ;
Jochum, W ;
Sibilia, M ;
Wagner, EF .
ONCOGENE, 2000, 19 (22) :2657-2663
[10]   Amino-terminal phosphorylation of c-Jun regulates stress-induced apoptosis and cellular proliferation [J].
Behrens, A ;
Sibilia, M ;
Wagner, EF .
NATURE GENETICS, 1999, 21 (03) :326-329