Transcription factors Elk-1 and SRF are engaged in IL1-dependent regulation of ZC3H12A expression

被引:62
作者
Kasza, Aneta [1 ]
Wyrzykowska, Paulina [1 ]
Horwacik, Irena [2 ]
Tymoszuk, Piotr [1 ]
Mizgalska, Danuta [1 ]
Palmer, Karren [3 ]
Rokita, Hanna [2 ]
Sharrocks, Andrew D. [3 ]
Jura, Jolanta [1 ]
机构
[1] Jagiellonian Univ, Dept Cell Biochem, Krakow, Poland
[2] Jagiellonian Univ, Lab Mol Genet & Virol, Krakow, Poland
[3] Univ Manchester, Fac Life Sci, Manchester, Lancs, England
来源
BMC MOLECULAR BIOLOGY | 2010年 / 11卷
基金
英国惠康基金;
关键词
NF-KAPPA-B; TERNARY COMPLEX; PROTEIN; INTERLEUKIN-1; INDUCTION; MECHANISM; APOPTOSIS; PATHWAY; CELLS; RNASE;
D O I
10.1186/1471-2199-11-14
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
Background: MCPIP is a novel CCCH zinc finger protein described as an RNase engaged in the regulation of immune responses. The regulation of expression of the gene coding for MCPIP - ZC3H12A is poorly explored. Results: Here we report that the proinflammatory cytokine IL-1 beta rapidly induces the synthesis of MCPIP in primary monocyte-derived macrophages and HepG2 cells. This up-regulation takes place through the MAP kinase pathway and following activation of the transcription factor Elk-1. Using a ZC3H12A reporter construct we have shown that a ZC3H12A promoter region, stretching from -76 to +60, mediates activation by IL-1 beta. This region contains binding sites for Elk-1 and its partner SRF. Chromatin immunoprecipitation analysis confirms in vivo binding of both transcription factors to this region of the ZC3H12A promoter. Conclusions: We conclude that the transcription factor Elk-1 plays an important role in the activation of ZC3H12A expression in response to IL-1 beta stimulation.
引用
收藏
页数:11
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