Programmed Cell Death during Plant Senescence - Postharvest Biology and Technology of Fruits, Vegetables, and Flowers - page 102

transcripts that were strongly upregulated by 4 ◦ C exposure are also induced by ethylene,
IAA, and JA but not by BA, and showed a typical SAG pattern during senescence.
Some elements of the signal transduction pathway upstream the transcription factors can
also be shared between different stresses and senescence. Thus, the senescence-associated
ZmMAPK5 is also induced during recovery after low-temperature stress (Berberich et al.,
1999).
5.10 Salicylic acid
Plants possess an immune system to defend themselves against pathogen infection. An
intensively studied inducible immune response occurs when a pathogen carrying an aviru-
lence ( avr ) gene is recognized directly or indirectly by a cognate resistance ( R ) gene in the
plant. This leads to activation of defenses that restrict pathogen growth in infected tissues
and in noninfected tissues by a process referred to as systemic acquired resistance (SAR).
These defense responses are typically accompanied by localized PCD around the site of
infection in the hypersensitive response (HR; Nimchuk et al., 2003). In the absence of an
R-avr interaction, basal resistance responses are also activated, although they may not suc-
cessfully restrict pathogen growth, and disease symptoms may develop (Glazebrook et al.,
1997).
The importance of salicylic acid (SA) in the induction of such resistance responses is
supported by both gain- and loss-of-function evidence. SA levels increase on many avirulent
and some virulent infections (Malamy et al., 1990; Metraux et al., 1990; Heck et al., 2003),
and application of exogenous SA, or generation of high endogenous SA levels by expression
of bacterial SA-synthesizing enzymes, is sufficient to induce resistance to many normally
virulent pathogens (White, 1979; Ward et al., 1991; Verberne et al., 2000; Mauch et al.,
2001). Loss-of-function analyses have relied on SA depletion by transgenic expression of
a bacterial SA hydroxylase encoded by nahG . NahG abrogates local R function elicited
by a range of bacterial, oomycete, and viral pathogens (Delaney et al., 1994; Rairdan and
Delaney, 2002) as well as SAR (Gaffney et al., 1993) and basal resistance responses to
virulent bacteria, fungi, and oomycetes (Delaney et al., 1994; Reuber et al., 1998). The
involvement of SA in activation of PCD in the HR is supported by similar lines of evidence
but remains less clear. SA does not induce HR-like PCD on its own in whole plants,
although it may induce PCD in cell culture (Kawai-Yamada et al., 2004). HR induced by
two Peronospora parasitica isolates avirulent on Arabidopsis appears to depend on SA,
since nahG blocked the HR in response to infection, although trailing necrosis surrounding
growing hyphae was still observed (Nawrath and Metraux, 1999). Similarly, nahG delays
the HR of tobacco ( Nicotiana tabacum ) in response to tobacco mosaic virus (Mur et al.,
1997). Consistent with these observations of PCD attenuation by SA removal, exogenous
SA strongly accelerated HR cell death in soybean ( Glycine max ) suspension cells (Shirasu
et al., 1997) and induced cell death in Arabidopsis lsd1 mutants and RPW8 -enhanced
transcription lines kept under conditions nonpermissive for spontaneous HR-like cell death
development (Dietrich et al., 1994; Xiao et al., 2003). Clearer evidence pointing to a role of
SA in PCD comes from the analysis of Arabidopsisacd and lsd mutants that spontaneously
activate PCD and defense responses. In many of these mutants, including acd6-1 , acd11 ,
ssi1 , and lsd6 , nahG expression completely suppresses PCD development, while this can
be restored by application of SA agonists such as 2,6-dichloroisonicotinic acid (INA) and