Transcriptional activation of the cyclin A gene by the architectural transcription factor HMGA2

被引:124
作者
Tessari, MA
Gostissa, M
Altamura, S
Sgarra, R
Rustighi, A
Salvagno, C
Caretti, G
Imbriano, C
Mantovani, R
Del Sal, G
Giancotti, V
Manfioletti, G
机构
[1] Univ Trieste, Dipartimento Biochim Biofis & Chim Macromol, I-34127 Trieste, Italy
[2] Univ Trieste, Ctr Excellence Biocristall, I-34127 Trieste, Italy
[3] Consorzio Interuniv Biotecnol, Lab Nazl, I-34012 Trieste, Italy
[4] Univ Udine, Dipartimento Patol & Med Sperimentale & Clin, I-33100 Udine, Italy
[5] Univ Modena & Reggio Emilia, Dipartimento Biol Anim, I-41100 Modena, Italy
关键词
D O I
10.1128/MCB.23.24.9104-9116.2003
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 HMGA2 protein belongs to the HMGA family of architectural transcription factors, which play an important role in chromatin organization. HMGA proteins are overexpressed in several experimental and human tumors and have been implicated in the process of neoplastic transformation. Hmga2 knockout results in the pygmy phenotype in mice and in a decreased growth rate of embryonic fibroblasts, thus indicating a role for HMGA2 in cell proliferation. Here we show that HMGA2 associates with the E1A-regulated transcriptional repressor p120(E4F), interfering with p120(E4F) binding to the cyclin A promoter. Ectopic expression of HMGA2 results in the activation of the cyclin A promoter and induction of the endogenous cyclin A gene. In addition, chromatin immunoprecipitation experiments show that HMGA2 associates with the cyclin A promoter only when the gene is transcriptionally activated. These data identify the cyclin A gene as a cellular target for HMGA2 and, for the first time, suggest a mechanism for HMGA2-dependent cell cycle regulation.
引用
收藏
页码:9104 / 9116
页数:13
相关论文
共 55 条
[1]   Transgenic mice expressing a truncated form of the high mobility group I-C protein develop adiposity and an abnormally high prevalence of lipomas [J].
Arlotta, P ;
Tai, AKF ;
Manfioletti, G ;
Clifford, C ;
Jay, G ;
Ono, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (19) :14394-14400
[2]  
ASHAR HR, 1995, CELL, V82, P57
[3]   Onset of natural killer cell lymphomas in transgenic mice carrying a truncated HMGI-C gene by the chronic stimulation of the IL-2 and IL-15 pathway [J].
Baldassarre, G ;
Fedele, M ;
Battista, S ;
Vecchione, A ;
Klein-Szanto, AJP ;
Santoro, M ;
Waldmann, TA ;
Azimi, N ;
Croce, CM ;
Fusco, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (14) :7970-7975
[4]  
Bandiera A, 1998, CANCER RES, V58, P426
[5]  
BARLAT I, 1995, ONCOGENE, V11, P1309
[6]  
Battista S, 1999, CANCER RES, V59, P4793
[7]  
BERLINGIERI MT, 1995, MOL CELL BIOL, V15, P1545
[8]   Cyclin A2 transcriptional regulation: Modulation of cell cycle control at the G1/S transition by peripheral cues [J].
Blanchard, JM .
BIOCHEMICAL PHARMACOLOGY, 2000, 60 (08) :1179-1184
[9]   Dynamic recruitment of NF-Y and histone acetyltransferases on cell-cycle promoters [J].
Caretti, G ;
Salsi, V ;
Vecchi, C ;
Imbriano, C ;
Mantovani, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (33) :30435-30440
[10]  
Chiappetta G, 1996, ONCOGENE, V13, P2439