A novel member of the BTB/POZ family, PATZ, associates with the RNF4 RING finger protein and acts as a transcriptional repressor

被引:76
作者
Fedele, M
Benvenuto, G
Pero, R
Majello, B
Battista, S
Lembo, F
Vollono, E
Day, PM
Santoro, M
Lania, L
Bruni, CB
Fusco, A
Chiariotti, L
机构
[1] Univ Naples Federico II, Dipartimento Biol & Patol Cellulare & Mol L Calif, CNR, Ctr Endocrinol & Oncol Sperimentale, I-80131 Naples, Italy
[2] Univ Naples Federico II, Dipartimento Genet Biol Mol & Gen, I-80134 Naples, Italy
[3] NCI, Cellular Oncol Lab, NIH, Bethesda, MD 20892 USA
[4] Univ Catanzaro Magna Graecia, Dipartimento Med Sperimentale & Clin G Salvatore, I-88100 Catanzaro, Italy
关键词
D O I
10.1074/jbc.275.11.7894
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
We have identified a novel human gene encoding a 59-kDa POZ-AT hook-zinc finger protein (PATZ) that interacts with RNF4, a mediator of androgen receptor activity, and acts as a transcriptional repressor. PATZ cDNA was isolated through a two-hybrid interaction screening using the RING finger protein RNF4 as a bait. In vitro and in vivo interaction between RNF4 and PATZ was demonstrated by protein-protein affinity chromatography and coimmunoprecipitation experiments. Such interaction occurred through a small region of PATZ containing an AT-hook DNA binding domain. Immunofluorescence staining and confocal microscopy showed that PATZ localizes in distinct punctate nuclear regions and colocalizes with RNF4. Functional analysis was pe;formed by cotransfection assays: PATZ acted as a transcriptional repressor, whereas its partner RNF4 behaved as a transcriptional activator. When both proteins were overexpressed a strong repression of the basal transcription was observed, indicating that the association of PATZ with RNF4 switches activation to repression, In addition, RNF4 was also found to associate with HMGI(Y), a chromatin-modeling factor containing AT-hook domains.
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收藏
页码:7894 / 7901
页数:8
相关论文
共 46 条
[11]   Amino-terminal protein-protein interaction motif (POZ-domain) is responsible for activities of the promyelocytic leukemia zinc finger retinoic acid receptor alpha fusion protein [J].
Dong, S ;
Zhu, J ;
Reid, A ;
Strutt, P ;
Guidez, F ;
Zhong, HJ ;
Wang, ZY ;
Licht, J ;
Waxman, S ;
Chomienne, C ;
Chen, Z ;
Zelent, A ;
Chen, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3624-3629
[12]   THE PML RETINOIC ACID RECEPTOR-ALPHA TRANSLOCATION CONVERTS THE RECEPTOR FROM AN INHIBITOR TO A RETINOIC ACID-DEPENDENT ACTIVATOR OF TRANSCRIPTION FACTOR-AP-1 [J].
DOUCAS, V ;
BROCKES, JP ;
YANIV, M ;
DETHE, H ;
DEJEAN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (20) :9345-9349
[13]   Truncated and chimeric HMGI-C genes induce neoplastic transformation of NIH3T3 murine fibroblasts [J].
Fedele, M ;
Berlingieri, MT ;
Scala, S ;
Chiariotti, L ;
Viglietto, G ;
Rippel, V ;
Bullerdiek, J ;
Santoro, M ;
Fusco, A .
ONCOGENE, 1998, 17 (04) :413-418
[14]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[15]   THE T(4-11) CHROMOSOME-TRANSLOCATION OF HUMAN ACUTE LEUKEMIAS FUSES THE ALL-1 GENE, RELATED TO DROSOPHILA-TRITHORAX, TO THE AF-4 GENE [J].
GU, Y ;
NAKAMURA, T ;
ALDER, H ;
PRASAD, R ;
CANAANI, O ;
CIMINO, G ;
CROCE, CM ;
CANAANI, E .
CELL, 1992, 71 (04) :701-708
[16]   Cell cycle regulated expression of mammalian CDC6 is dependent on E2F [J].
Hateboer, G ;
Wobst, A ;
Petersen, BO ;
Le Cam, L ;
Vigo, E ;
Sardet, C ;
Helin, K .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6679-6697
[17]   The BCL-6 POZ domain and other POZ domains interact with the co-repressors N-CoR and SMRT [J].
Huynh, KD ;
Bardwell, VJ .
ONCOGENE, 1998, 17 (19) :2473-2484
[18]  
JOHNSON PF, 1989, ANNU REV BIOCHEM, V58, P799, DOI 10.1146/annurev.biochem.58.1.799
[19]   CHROMOSOMAL TRANSLOCATION T(15-17) IN HUMAN ACUTE PROMYELOCYTIC LEUKEMIA FUSES RAR-ALPHA WITH A NOVEL PUTATIVE TRANSCRIPTION FACTOR, PML [J].
KAKIZUKA, A ;
MILLER, WH ;
UMESONO, K ;
WARRELL, RP ;
FRANKEL, SR ;
MURTY, VVVS ;
DMITROVSKY, E ;
EVANS, RM .
CELL, 1991, 66 (04) :663-674
[20]   MEL-18, A POLYCOMB GROUP-RELATED MAMMALIAN GENE, ENCODES A TRANSCRIPTIONAL NEGATIVE REGULATOR WITH TUMOR SUPPRESSIVE ACTIVITY [J].
KANNO, M ;
HASEGAWA, M ;
ISHIDA, A ;
ISONO, K ;
TANIGUCHI, M .
EMBO JOURNAL, 1995, 14 (22) :5672-5678