Abstract

The promoter of the murine gene encoding inducible nitric oxide synthase (iNOS) contains an NF-kappa B site beginning 55 base pairs upstream of the TATA box, designated NF-kappa Bd. Reporter constructs containing truncated promoter regions, when transfected into macrophages, revealed that NF-kappa Bd is necessary to confer inducibility by bacterial lipopolysaccharide (LPS). Oligonucleotide probes containing NF-kappa Bd plus the downstream 9 or 47 base pairs bound proteins that rapidly appeared in the nuclei of LPS-treated macrophages. The nuclear proteins bound to both probes in an NF-kappa Bd-dependent manner, but binding was resistant to cycloheximide only for the shorter probe. The proteins binding both probes reacted with antibodies against p50 and c-rel but not RelB; those binding the shorter probe also reacted with anti-RelA (p65). Pyrrolidine dithiocarbamate, which acts as a specific inhibitor of NF-kappa B, blocked both the activation of the NF-kappa Bd-binding proteins and the production of NO in LPS-treated macrophages. Thus, activation of NF-kappa B/Rel is critical in the induction of iNOS by LPS. However, additional, newly synthesized proteins contribute to the NF-kappa Bd-dependent transcription factor complex on the iNOS promoter in LPS-treated mouse macrophages.

Highlights

  • Qiao-wen XieS,Yuki Kashiwabara, and Carl Nathan sus sequences for the binding of transcription factors involved i n the inducibility of other genes by cytokines aLnPdS.Among these are two putative NF-KB binding sites, one upstream

  • One clone contained plasmid p8.liNOS-containing trun- icol acetyltransferase (CAT), which had a deletion of 407 bp (-492 to -86) from pliNOS-CAT,generating a SmaI site adjacent to the 5' end ofNF-KBd

  • In contrast,no supershift wasobserved with segment of the identicatlo the NF-KB sitein nitric oxide synthase (iNOS) promoter

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Summary

Oxide Synthase*

The recently cloned promoterof the murine gene coding for iNOS [11] contains at least 22 elements homologous to consen-. One clone contained plasmid p8.liNOS-CAT, which had a deletion of 407 bp (-492 to -86) from pliNOS-CAT,generating a SmaI site adjacent to the 5' end ofNF-KBd. The promoter region upstream of this SmaI site was removed to form p8.1lNOS-CAT.To construct p8.13iNOS-CAT, the region -75 to +161 was amplified bypo-. OLIGOMAER cells; CAT, chloramphenicol acetyltransferase; EMSA, electrophoretic mobility shift assay; IFN-1, interferon-gamma;LPS, endotoxicbacterial lipopolysaccharide; NF-KB,nuclear factor for immunoglobulin K chain in B cells; PDTC, pyrrolidine dithiocarbamate; bp, base pair(s). Products were electrophoresedat 30 mAfor h on 4.8% polyacrylamide gels in high ionic strength buffer (50 mM Tris, 380 mM glycine, 2 mM EDTA, pH -8.5) [14] and dried gels analyzedby autoradiography

RESULTS
Probe A
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