STAT1 является членом семейства транскрипционных факторовпреобразователей сигналов и активаторов транскрипции[en] . STAT1 участвует в положительной регуляции генов по сигналам интерферона либо типа I, типа II, или типа III. В ответ на IFN-γ стимуляцию, STAT1 образует гомодимеры или гетеродимеры с STAT3, которые связываются с GAS (Interferon G amma- A ctivated S equence) промоторным элементом; В ответ на любую IFN-α или IFN-β стимуляцию, STAT1 образует гетеродимер с STAT2, который может связываться с ISRE ( I nterferon- S timulated R esponse E lement) промоторным элементом.[1] В любом случае, связывание элемента с промотором приводит к увеличению экспрессии ISG ( I nterferon- S timulated G enes).
↑ Katze MG, He Y, et al. (2002). “Viruses and interferon: a fight for supremacy”. Nature Reviews Immunology. 2 (9): 675—87. DOI:10.1038/nri888. PMID12209136.Неизвестный параметр |author-separator= (справка)
↑ Lu HF, Yang JS, Lin YT, Tan TW, Ip SW, Li YC, Tsou MF, Chung JG (2007). “Diallyl disulfide induced signal transducer and activator of transcription 1 expression in human colon cancer colo 205 cells using differential display RT-PCR”. Cancer Genomics Proteomics. 4 (2): 93—7. PMID17804871.
1 2 Olayioye MA, Beuvink I, Horsch K, Daly JM, Hynes NE (June 1999). “ErbB receptor-induced activation of stat transcription factors is mediated by Src tyrosine kinases”. J. Biol. Chem. 274 (24): 17209–18. PMID10358079.
1 2 Xia L, Wang L, Chung AS, Ivanov SS, Ling MY, Dragoi AM, Platt A, Gilmer TM, Fu XY, Chin YE (August 2002). “Identification of both positive and negative domains within the epidermal growth factor receptor COOH-terminal region for signal transducer and activator of transcription (STAT) activation”. J. Biol. Chem. 277 (34): 30716–23. DOI:10.1074/jbc.M202823200. PMID12070153.
↑ Reuter TY, Medhurst AL, Waisfisz Q, Zhi Y, Herterich S, Hoehn H, Gross HJ, Joenje H, Hoatlin ME, Mathew CG, Huber PA (October 2003). “Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transport”. Exp. Cell Res. 289 (2): 211–21. PMID14499622.
↑ Pang Q, Christianson TA, Keeble W, Diaz J, Faulkner GR, Reifsteck C, Olson S, Bagby GC (September 2001). “The Fanconi anemia complementation group C gene product: structural evidence of multifunctionality”. Blood. 98 (5): 1392–401. PMID11520787.
1 2 Usacheva A, Smith R, Minshall R, Baida G, Seng S, Croze E, Colamonici O (June 2001). “The WD motif-containing protein receptor for activated protein kinase C (RACK1) is required for recruitment and activation of signal transducer and activator of transcription 1 through the type I interferon receptor”. J. Biol. Chem. 276 (25): 22948–53. DOI:10.1074/jbc.M100087200. PMID11301323.
↑ Usacheva A, Tian X, Sandoval R, Salvi D, Levy D, Colamonici OR (September 2003). “The WD motif-containing protein RACK-1 functions as a scaffold protein within the type I IFN receptor-signaling complex”. J. Immunol. 171 (6): 2989–94. PMID12960323.
↑ Chatterjee-Kishore M, van Den Akker F, Stark GR (July 2000). “Adenovirus E1A down-regulates LMP2 transcription by interfering with the binding of stat1 to IRF1”. J. Biol. Chem. 275 (27): 20406–11. DOI:10.1074/jbc.M001861200. PMID10764778.
↑ Takeda A, Hamano S, Yamanaka A, Hanada T, Ishibashi T, Mak TW, Yoshimura A, Yoshida H (May 2003). “Cutting edge: role of IL-27/WSX-1 signaling for induction of T-bet through activation of STAT1 during initial Th1 commitment”. J. Immunol. 170 (10): 4886–90. PMID12734330.
1 2 Kristof AS, Marks-Konczalik J, Billings E, Moss J (September 2003). “Stimulation of signal transducer and activator of transcription-1 (STAT1)-dependent gene transcription by lipopolysaccharide and interferon-gamma is regulated by mammalian target of rapamycin”. J. Biol. Chem. 278 (36): 33637–44. DOI:10.1074/jbc.M301053200. PMID12807916.
↑ Wong AH, Durbin JE, Li S, Dever TE, Decker T, Koromilas AE (April 2001). “Enhanced antiviral and antiproliferative properties of a STAT1 mutant unable to interact with the protein kinase PKR”. J. Biol. Chem. 276 (17): 13727–37. DOI:10.1074/jbc.M011240200. PMID11278865.
↑ Li X, Leung S, Qureshi S, Darnell JE, Stark GR (March 1996). “Formation of STAT1-STAT2 heterodimers and their role in the activation of IRF-1 gene transcription by interferon-alpha”. J. Biol. Chem. 271 (10): 5790–4. PMID8621447.
↑ Dumler I, Kopmann A, Wagner K, Mayboroda OA, Jerke U, Dietz R, Haller H, Gulba DC (August 1999). “Urokinase induces activation and formation of Stat4 and Stat1-Stat2 complexes in human vascular smooth muscle cells”. J. Biol. Chem. 274 (34): 24059–65. PMID10446176.
↑ Fagerlund R, Mélen K, Kinnunen L, Julkunen I (August 2002). “Arginine/lysine-rich nuclear localization signals mediate interactions between dimeric STATs and importin alpha 5”. J. Biol. Chem. 277 (33): 30072–8. DOI:10.1074/jbc.M202943200. PMID12048190.
↑ Gunaje JJ, Bhat GJ (October 2001). “Involvement of tyrosine phosphatase PTP1D in the inhibition of interleukin-6-induced Stat3 signaling by alpha-thrombin”. Biochem. Biophys. Res. Commun. 288 (1): 252–7. DOI:10.1006/bbrc.2001.5759. PMID11594781.
↑ Spiekermann K, Biethahn S, Wilde S, Hiddemann W, Alves F (August 2001). “Constitutive activation of STAT transcription factors in acute myelogenous leukemia”. Eur. J. Haematol. 67 (2): 63–71. PMID11722592.
↑ Cirri P, Chiarugi P, Marra F, Raugei G, Camici G, Manao G, Ramponi G (October 1997). “c-Src activates both STAT1 and STAT3 in PDGF-stimulated NIH3T3 cells”. Biochem. Biophys. Res. Commun. 239 (2): 493–7. DOI:10.1006/bbrc.1997.7493. PMID9344858.
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