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研究生:張峰銓
研究生(外文):Feng-Chuan Chang
論文名稱:PKA對RNF4的磷酸化可促進含有CCAAT-box基因的轉錄表現
論文名稱(外文):Phosphorylation of RNF4 by protein kinase A contributes to CCAAT-box related transcription
指導教授:李玉梅李玉梅引用關係
指導教授(外文):Yu-May Lee
學位類別:碩士
校院名稱:國立臺灣大學
系所名稱:生化科學研究所
學門:生命科學學門
學類:生物科技學類
論文種類:學術論文
論文出版年:2006
畢業學年度:94
語文別:英文
論文頁數:61
中文關鍵詞:協同抑制因子活化因子磷酸化
外文關鍵詞:RNF4PKAphosphorylation
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RNF4 是一種在C端具有RING finger 的蛋白,目前已知可以藉由與細胞核中的不同蛋白作用來調控基因的轉錄表現;RNF4被認為是轉錄機制中的協同抑制因子或是活化因子。根據我們過去的研究,我們發現RNF4參與GCH此基因的轉錄表現,而且這樣的活化過程是藉由GCH基因上游啟動子中的CCAAT-box來達成。由於RNF4對於CCAAT-box 此區域並沒有專一性的辨認,所以我們認為RNF4是透過輔助CCAAT-box專一性蛋白的NF-Y來達成此轉錄機轉。綜合來說,我們認為RNF4在GCH基因上的啟動子扮演重要的角色。
在這次的研究中,我發現藉由蛋白質激酶PKA對RNF4的磷酸化可以促進含有CCAAT-box的GCH基因轉錄表現。從實驗上的結果,我們知道突變態的RNF4蛋白會影響蛋白質激酶PKA對RNF4的磷酸化,而進一步影響RNF4在GCH基因上的活化表現。我也發現S127、S166是蛋白質激酶PKA磷酸化的重要位置。除此之外,我還發現RNF4蛋白的C端鹼性區域對於其本身的活化與受到PKA的磷酸化相當重要。
總結來說,我們首次證明RNF4是受到訊息傳遞中的蛋白質激酶PKA磷酸化進而活化GCH基因的表現。
The small nuclear RING finger protein 4 (RNF4) is a recently identified human RING finger protein that contains C3HC4-type zinc finger motif in the C-terminal region. RNF4 has been implicated in transcriptional regulation through interacting with a variety of nuclear proteins, and functions as a transcriptional corepressor or coactivator.
According to our previous study, we found that coactivator RNF4 is involved in the GTP cyclohydrolase I (GCH) gene expression and we defined the RNF4-responsive element on GCH proximal promoter as a CCAAT-box. RNF4 did not possess specific DNA binding activity toward this CCAAT box, which suggests that RNF4 is a coactivator of the CCAAT box binding protein nuclear factor Y (NF-Y). Overall, we prove that RNF4 imposes functional importance on GCH promoter.
In this study, I demonstrated that protein kinase A (PKA)-dependent phosphorylation of RNF4 activates the CCAAT-box containing GCH promoter. Results from biological and functional characterizations of RNF4 mutants defective in PKA phosphorylation sites suggest that PKA-dependent RNF4 phosphorylation is important for its role in GCH promoter activation. S127 and S166 of RNF4 are important phosphorylation sites in RNF4-mediated CAAT-box activation by PKA. Furthermore, I also found that the C-terminal basic region is essential for RNF4 phosphorylation and activation by PKA.
In summary, we first illustrate a novel RNF4-mediated PKA signaling pathway that leads to the activation of GCH promoter.
EnglishAbstract……………………………………………………………………...3
ChineseAbstract……………………………………………………………………..4
Abbreviations…………………………………………………………………………5
1. Introduction
1.1 RNF4 …...……….………………………………………………………………...6
1.2 The RING finger motif…………………………………………………………….8
1.3 GTP cyclohydrolaseⅠ…………………………………………………………..10
1.4 RNF4 and GCH promoter………………………………………………………..12
1.5 CCAAT-Box……………………………………………………………………...13
1.6 NF-Y……………………………………………………………………………..14
1.7 RNF4 and NF-Y………………………………………………………………….16
1.8 PKA pathway……………………………………………………………………..16
2. Material and Methods
2.1 Plasmid constructs………………………………………………………………..19
2.2 Cell culture……………………………………………………………………….19
2.3 Plasmid DNA purification………………………………………………………..20
2.4 Expression and Purification of Fusion Protein…………………………………...21
2.5 In vitro phosphorylation………………………………………………………….21
2.6 Transfection………………………………………………………………………22
2.7 Transient transfection…………………………………………………………….22
2.8 Transcriptional Activation and Luciferase Assay………………………………...23
2.9 Transformation…………………………………………………………………...23
2.10 In vitro translation………………………………………………………………23
3. Results
3.1 Forskolin up-regulates the activity of RNF4 through CCAAT-box……………...24
3.2 RNF4 is phosphorylated in cells…………………………………………………25
3.3 RNF4 is phosphorylated by PKA in vitro………………………………………..26
3.4 Identification of RNF4 residues phosphorylated by PKA……………………….26
3.5 PKA-mediated RNF4 activation of the CCAAT-box by phosphorylation on S127 and S166………………………………………………………………………….27
3.6 Cross-talk to MAPK signaling induction by PKA pathways…………………….28
3.7 The C-terminal basic region is essential for RNF4 phosphorylation and activation by PKA…………………………………………………………………………...29
3.8 Interaction with TBP is increased by RNF4 phosphorylation…………………....30
4. Discussion
4.1 Phosphorylation of RNF4 could contribute to CCAAT-box related transcription………………………………………………………………………31
4.2 Possible mechanisms for phospho-RNF4 mediated enhancement of CCAAT-box………………………………………………………………………32
4.3 MAPK signaling pathway may play a role in regulating the activity of RNF4….33
4.4 Other biological function of phosphrylated RNF4……………………………….34
5. Reference……………..........................................................................................35
6. Figure……………………………………………………………………………40
7. Appendix………………………………………………………………………..53
Baxevanis, A. D., G. Arents, et al. (1995). "A variety of DNA-binding and multimeric proteins contain the histone fold motif." Nucleic Acids Res 23(14): 2685-91.
Blau, N. and A. Niederwieser (1985). "GTP-cyclohydrolases: a review." J Clin Chem Clin Biochem 23(4): 169-76.
Carthew, R. W. and G. M. Rubin (1990). "seven in absentia, a gene required for specification of R7 cell fate in the Drosophila eye." Cell 63(3): 561-77.
Chiariotti, L., G. Benvenuto, et al. (1998). "Identification and characterization of a novel RING-finger gene (RNF4) mapping at 4p16.3." Genomics 47(2): 258-65.
Currie, R. A. (1998). "NF-Y is associated with the histone acetyltransferases GCN5 and P/CAF." J Biol Chem 273(3): 1430-4.
Daniel, P. B., W. H. Walker, et al. (1998). "Cyclic AMP signaling and gene regulation." Annu Rev Nutr 18: 353-83.
Daniel, P. T., C. Scholz, et al. (1998). "Dendritic cells prevent CD95 mediated T lymphocyte death through costimulatory signals." Adv Exp Med Biol 451: 173-7.
Dorn, A., J. Bollekens, et al. (1987). "A multiplicity of CCAAT box-binding proteins." Cell 50(6): 863-72.
Farina, A., I. Manni, et al. (1999). "Down-regulation of cyclin B1 gene transcription in terminally differentiated skeletal muscle cells is associated with loss of functional CCAAT-binding NF-Y complex." Oncogene 18(18): 2818-27.
Fedele, M., G. Benvenuto, et al. (2000). "A novel member of the BTB/POZ family, PATZ, associates with the RNF4 RING finger protein and acts as a transcriptional repressor." J Biol Chem 275(11): 7894-901.
Freemont, P. S. (1993). "The RING finger. A novel protein sequence motif related to the zinc finger." Ann N Y Acad Sci 684: 174-92.
Galili, N., S. Nayak, et al. (2000). "Rnf4, a RING protein expressed in the developing nervous and reproductive systems, interacts with Gscl, a gene within the DiGeorge critical region." Dev Dyn 218(1): 102-11.
Graves, L. M., K. E. Bornfeldt, et al. (1997). "Historical perspectives and new insights involving the MAP kinase cascades." Adv Second Messenger Phosphoprotein Res 31: 49-62.
Hafner, S., H. S. Adler, et al. (1994). "Mechanism of inhibition of Raf-1 by protein kinase A." Mol Cell Biol 14(10): 6696-703.
Hagiwara, M., A. Alberts, et al. (1992). "Transcriptional attenuation following cAMP induction requires PP-1-mediated dephosphorylation of CREB." Cell 70(1): 105-13.
Hagiwara, M., P. Brindle, et al. (1993). "Coupling of hormonal stimulation and transcription via the cyclic AMP-responsive factor CREB is rate limited by nuclear entry of protein kinase A." Mol Cell Biol 13(8): 4852-9.
Hakli, M., U. Karvonen, et al. (2001). "The RING finger protein SNURF is a bifunctional protein possessing DNA binding activity." J Biol Chem 276(26): 23653-60.
Hakli, M., U. Karvonen, et al. (2005). "SUMO-1 promotes association of SNURF (RNF4) with PML nuclear bodies." Exp Cell Res 304(1): 224-33.
Hakli, M., K. L. Lorick, et al. (2004). "Transcriptional coregulator SNURF (RNF4) possesses ubiquitin E3 ligase activity." FEBS Lett 560(1-3): 56-62.
Hanson, I. M., A. Poustka, et al. (1991). "New genes in the class II region of the human major histocompatibility complex." Genomics 10(2): 417-24.
Hirano, M., T. Yanagihara, et al. (1998). "Dominant negative effect of GTP cyclohydrolase I mutations in dopa-responsive hereditary progressive dystonia." Ann Neurol 44(3): 365-71.
Hirayama, K. and G. Kapatos (1998). "Nigrostriatal dopamine neurons express low levels of GTP cyclohydrolase I protein." J Neurochem 70(1): 164-70.
Hofmann, K., P. Bucher, et al. (1999). "The PROSITE database, its status in 1999." Nucleic Acids Res 27(1): 215-9.
Houslay, M. D. and D. R. Adams (2003). "PDE4 cAMP phosphodiesterases: modular enzymes that orchestrate signalling cross-talk, desensitization and compartmentalization." Biochem J 370(Pt 1): 1-18.
Houslay, M. D. and G. S. Baillie (2003). "The role of ERK2 docking and phosphorylation of PDE4 cAMP phosphodiesterase isoforms in mediating cross-talk between the cAMP and ERK signalling pathways." Biochem Soc Trans 31(Pt 6): 1186-90.
Houslay, M. D. and W. Kolch (2000). "Cell-type specific integration of cross-talk between extracellular signal-regulated kinase and cAMP signaling." Mol Pharmacol 58(4): 659-68.
Hwu, W. L., Y. W. Chiou, et al. (2000). "Dopa-responsive dystonia is induced by a dominant-negative mechanism." Ann Neurol 48(4): 609-13.
Hwu, W. L., M. Y. Lu, et al. (2004). "Molecular chaperones affect GTP cyclohydrolase I mutations in dopa-responsive dystonia." Ann Neurol 55(6): 875-8.
Ichinose, H., T. Ohye, et al. (1994). "Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene." Nat Genet 8(3): 236-42.
Imbriano, C., F. Bolognese, et al. (2001). "HSP-CBF is an NF-Y-dependent coactivator of the heat shock promoters CCAAT boxes." J Biol Chem 276(28): 26332-9.
Jung, M. S., J. Yun, et al. (2001). "p53 and its homologues, p63 and p73, induce a replicative senescence through inactivation of NF-Y transcription factor." Oncogene 20(41): 5818-25.
Kaiser, F. J., T. Moroy, et al. (2003). "The RING finger protein RNF4, a co-regulator of transcription, interacts with the TRPS1 transcription factor." J Biol Chem 278(40): 38780-5.
Kuo, C. T. and J. M. Leiden (1999). "Transcriptional regulation of T lymphocyte development and function." Annu Rev Immunol 17: 149-87.
Li, X. Y., R. Hooft van Huijsduijnen, et al. (1992). "Intron-exon organization of the NF-Y genes. Tissue-specific splicing modifies an activation domain." J Biol Chem 267(13): 8984-90.
Lorick, K. L., J. P. Jensen, et al. (1999). "RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination." Proc Natl Acad Sci U S A 96(20): 11364-9.
Lovering, R., I. M. Hanson, et al. (1993). "Identification and preliminary characterization of a protein motif related to the zinc finger." Proc Natl Acad Sci U S A 90(6): 2112-6.
Maity, S. N. and B. de Crombrugghe (1998). "Role of the CCAAT-binding protein CBF/NF-Y in transcription." Trends Biochem Sci 23(5): 174-8.
Manning, G., D. B. Whyte, et al. (2002). "The protein kinase complement of the human genome." Science 298(5600): 1912-34.
Mantovani, R. (1998). "A survey of 178 NF-Y binding CCAAT boxes." Nucleic Acids Res 26(5): 1135-43.
Marziali, G., E. Perrotti, et al. (1999). "The activity of the CCAAT-box binding factor NF-Y is modulated through the regulated expression of its A subunit during monocyte to macrophage differentiation: regulation of tissue-specific genes through a ubiquitous transcription factor." Blood 93(2): 519-26.
Marziali, G., E. Perrotti, et al. (1997). "Transcriptional regulation of the ferritin heavy-chain gene: the activity of the CCAAT binding factor NF-Y is modulated in heme-treated Friend leukemia cells and during monocyte-to-macrophage differentiation." Mol Cell Biol 17(3): 1387-95.
Matuoka, K. and K. Yu Chen (1999). "Nuclear factor Y (NF-Y) and cellular senescence." Exp Cell Res 253(2): 365-71.
Moilanen, A. M., H. Poukka, et al. (1998). Identification of a novel RING finger protein as a coregulator in steroid receptor-mediated gene transcription. Mol Cell Biol.
Morgan, D. O. (1995). "Principles of CDK regulation." Nature 374(6518): 131-4.
Nichol, C. A., G. K. Smith, et al. (1985). "Biosynthesis and metabolism of tetrahydrobiopterin and molybdopterin." Annu Rev Biochem 54: 729-64.
Pang, J. H. and K. Y. Chen (1993). "A specific CCAAT-binding protein, CBP/tk, may be involved in the regulation of thymidine kinase gene expression in human IMR-90 diploid fibroblasts during senescence." J Biol Chem 268(4): 2909-16.
Pero, R., F. Lembo, et al. (2001). "RNF4 is a growth inhibitor expressed in germ cells but not in human testicular tumors." Am J Pathol 159(4): 1225-30.
Poukka, H., P. Aarnisalo, et al. (2000). "Coregulator small nuclear RING finger protein (SNURF) enhances Sp1- and steroid receptor-mediated transcription by different mechanisms." J Biol Chem 275(1): 571-9.
Poukka, H., U. Karvonen, et al. (2000). "The RING finger protein SNURF modulates nuclear trafficking of the androgen receptor." J Cell Sci 113 (Pt 17): 2991-3001.
Reddy, B. A., M. Kloc, et al. (1991). "The cloning and characterization of a maternally expressed novel zinc finger nuclear phosphoprotein (xnf7) in Xenopus laevis." Dev Biol 148(1): 107-16.
Ronchi, A., M. Bellorini, et al. (1995). "CCAAT-box binding protein NF-Y (CBF, CP1) recognizes the minor groove and distorts DNA." Nucleic Acids Res 23(22): 4565-72.
Saurin, A. J., K. L. Borden, et al. (1996). "Does this have a familiar RING?" Trends Biochem Sci 21(6): 208-14.
Shimizu, S., M. Ishii, et al. (1999). "Presence of excess tetrahydrobiopterin during nitric oxide production from inducible nitric oxide synthase in LPS-treated rat aorta." Life Sci 65(26): 2769-79.
Sinha, S., I. S. Kim, et al. (1996). "Three classes of mutations in the A subunit of the CCAAT-binding factor CBF delineate functional domains involved in the three-step assembly of the CBF-DNA complex." Mol Cell Biol 16(1): 328-37.
Suzuki, T., T. Ohye, et al. (1999). "Characterization of wild-type and mutants of recombinant human GTP cyclohydrolase I: relationship to etiology of dopa-responsive dystonia." J Neurochem 73(6): 2510-6.
Takeuchi, M., M. Rothe, et al. (1996). "Anatomy of TRAF2. Distinct domains for nuclear factor-kappaB activation and association with tumor necrosis factor signaling proteins." J Biol Chem 271(33): 19935-42.
Tasken, K. and E. M. Aandahl (2004). "Localized effects of cAMP mediated by distinct routes of protein kinase A." Physiol Rev 84(1): 137-67.
Torgersen, K. M., T. Vang, et al. (2002). "Molecular mechanisms for protein kinase A-mediated modulation of immune function." Cell Signal 14(1): 1-9.
Wu, J., P. Dent, et al. (1993). "Inhibition of the EGF-activated MAP kinase signaling pathway by adenosine 3'',5''-monophosphate." Science 262(5136): 1065-9.
Wu, L. C., Z. W. Wang, et al. (1996). "Identification of a RING protein that can interact in vivo with the BRCA1 gene product." Nat Genet 14(4): 430-40.
Wu, S. M., W. C. Kuo, et al. (2004). "RNF4 is a coactivator for nuclear factor Y on GTP cyclohydrolase I proximal promoter." Mol Pharmacol 66(5): 1317-24.
Yan, W., S. J. Hirvonen-Santti, et al. (2002). "Expression of the nuclear RING finger protein SNURF/RNF4 during rat testis development suggests a role in spermatid maturation." Mech Dev 118(1-2): 247-53.
Yang, S. H., A. D. Sharrocks, et al. (2003). "Transcriptional regulation by the MAP kinase signaling cascades." Gene 320: 3-21.
Zwicker, J., F. C. Lucibello, et al. (1995). "Cell cycle regulation of the cyclin A, cdc25C and cdc2 genes is based on a common mechanism of transcriptional repression." Embo J 14(18): 4514-22.
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