LGP2 Expression is Enhanced by Interferon Regulatory Factor 3 in Olive Flounder, Paralichthys olivaceus

被引:17
|
作者
Hikima, Jun-ichi [1 ]
Yi, Mi-Kyong [1 ]
Ohtani, Maki [1 ]
Jung, Chan Yong [1 ]
Kim, Young Kyu [1 ]
Mun, Ji Young [1 ]
Kim, Young Rim [1 ]
Takeyama, Haruko [2 ]
Aoki, Takashi [1 ,3 ]
Jung, Tae Sung [1 ]
机构
[1] Gyeongsang Natl Univ, Aquat Biotechnol Ctr, Coll Vet Med, Jinju, Gyeongnam, South Korea
[2] Waseda Univ, Dept Life Sci & Med Biosci, Shinjuku Ku, Tokyo, Japan
[3] Waseda Univ, Consolidated Res Inst Adv Sci & Med Care ASMeW, Shinjuku Ku, Tokyo, Japan
来源
PLOS ONE | 2012年 / 7卷 / 12期
关键词
I-LIKE-RECEPTORS; DOUBLE-STRANDED-RNA; INDUCIBLE GENE-I; RIG-I; JAPANESE FLOUNDER; FUNCTIONAL-CHARACTERIZATION; ANTIVIRAL RESPONSES; ATLANTIC COD; RECOGNITION; ACTIVATION;
D O I
10.1371/journal.pone.0051522
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In innate immunity, LGP2 (laboratory of genetics and physiology 2) plays a very important role in the production of type I interferon (IFN) through recognition of cytosolic viral RNA. Although viral infection or stimulation with double-strand RNA dramatically induces expression of the LGP2 gene, the underlying transcriptional mechanism has never been studied. Here, we cloned and characterized the 5'-upstream region (-1,337 bp) of the LGP2 gene in olive flounder (Paralichthys olivaceus). Numerous canonical motifs for IFN-regulatory factors (IRFs) were found in this region, and reporter assays identified a poly I: C-responsive promoter region (-506 to -398) that regulated LGP2 transcription. Transcriptional activity of the LGP2 promoter was strongly enhanced by IRF3, which bound to IRF3 motif #3 (-480). The LGP2 promoter was also responsive to viral infection in vitro. These results suggest that LGP2 transcriptional control is crucially involved to regulated by IRF3 function after viral infection or stimulation with poly I:C.
引用
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页数:12
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