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A Novel NF-κB Binding Site Controls Human Granzyme B Gene Transcription
Author(s) -
Chunjian Huang,
Enguang Bi,
Yu Hu,
Weiwen Deng,
Zhigang Tian,
Chen Dong,
Yuanjie Hu,
Bing Sun
Publication year - 2006
Publication title -
the journal of immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.176.7.4173
Subject(s) - granzyme , chromatin immunoprecipitation , jurkat cells , granzyme b , transcription factor , biology , microbiology and biotechnology , binding site , luciferase , transcription (linguistics) , transcriptional regulation , gene expression , gene , in vitro , cytotoxicity , t cell , promoter , genetics , transfection , immune system , perforin , linguistics , philosophy
Granzyme B expression is essential for eliciting NK cell cytotoxicity and T cell function. However, its transcriptional regulatory mechanism is not well understood. In this report, we demonstrate in human NK cells and T cells that the NF-kappaB-signaling pathway is involved in such control. Furthermore, a novel downstream human granzyme B gene sequence (GGAGATTCCC) was identified for NF-kappaB binding. EMSA, luciferase, and chromatin immunoprecipitation assays in vitro and in vivo indicated that this NF-kappaB binding site is functional in an NK cell line and its primary counterpart. Our data also demonstrate that this binding site is functional in Jurkat T cells. Taken together, we identified a novel NF-kappaB binding site, which plays a pivotal role in controlling human granzyme B gene transcription.

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