Salicylic acid (SA) plays a critical signaling role in the activation of pl
ant defense responses after pathogen attack. We have identified several pot
ential components of the SA signaling pathway, including (i) the H2O2-scave
nging enzymes catalase and ascorbate peroxidase. (ii) a high affinity SA-bi
nding protein (SABP2), (iii) a SA-inducible protein kinase (SIPK), (iv) NPR
1, an ankyrin repeat-containing protein that exhibits limited homology to I
kappa B alpha and is required for SA signaling, and (v) members of the TGA
/OBF family of bZIP transcription factors. These bZIP factors physically in
teract with NPR1 and bind the SA-responsive element in promoters of several
defense genes, such as the pathogenesis-related 1 gene (PR-1). Recent stud
ies have demonstrated that nitric oxide (NO) is another signal that activat
es defense responses after pathogen attack. NO has been shown to play a cri
tical role in the activation of innate immune and inflammatory responses in
animals. Increases in NO synthase (NOS)-like activity occurred in resistan
t but not susceptible tobacco after infection with tobacco mosaic virus. He
re we demonstrate that this increase in activity participates in PR-1 gene
induction. Two signaling molecules, cGMP and cyclic ADP ribose (cADPR), whi
ch function downstream of NO in animals, also appear to mediate plant defen
se gene activation (e.g., PR-1). Additionally, NO may activate PR-1 express
ion via an NO-dependent, cADPR-independent pathway. Several targets of NO i
n animals, including guanylate cyclase, aconitase, and mitogen-activated pr
otein kinases (e.g., SIPK), are also modulated by NO in plants. Thus, at le
ast portions of NO signaling pathways appear to be shared between plants an
d animals.