Programmed Cell Death during Plant Senescence - Postharvest Biology and Technology of Fruits, Vegetables, and Flowers - page 89

calcium is associated with leaf senescence in parsley (Huang et al., 1997), and calcium fluxes
have also been implicated in two other leaf senescence systems (Chou and Kao, 1992; He
and Jin, 1999). Thus, calcium signaling may play a role in leaf PCD although further data
are needed. Cytologically, PCD has been charted in rice leaves undergoing induced (by dark
treatment) or natural senescence (Lee and Chen, 2002). In this system, features noted were
cytoplasm depletion, organellar breakdown, and expansion of the central vacuole, which
at later stages contained inclusions possibly of chloroplast origin. Chromatin condensation
was not noted, nor apoptotic bodies, and although cells became terminal deoxynucleotidyl
transferase biotin-dUTP nick end labeling (TUNEL) positive and DNA became increasingly
degraded, there was no evidence of DNA laddering. However DNA laddering was detected in
senescing leaves of other species such as wheat (Caccia et al., 2001), olive (Cao et al., 2003),
and five other tree species (Yen and Yang, 1998). Chromatin condensation was also reported
in both tobacco and the monocot Ornithogalum virens (Simeonova et al., 2000). There
was no clear reduction in mitochondrial membrane potentials in Pisum sativum mesophyll
cells undergoing senescence (Simeonova et al., 2004) indicating that if mitochondria are
associated with this PCD system it is not in the same way as in animal apoptosis. Chloroplast
disassembly seems to be an early sign of senescence, but whether this is part of the PCD
mechanism remains uncertain (Thomas et al., 2003).
Petal senescence unlike leaf senescence inevitably ends with PCD. Genomic approaches
are being used to identify genes involved in petal senescence (Breeze et al., 2004) and the
expression of several of the known homologs of the animal PCD-related genes, namely, Be-
clin, Bax inhibitor I, and dad-1 (Orzaez and Granell, 1997a, b; Wagstaff et al., 2003; Huck-
elhoven, 2004). Evidence from electron microscopy from Alstroemeria senescent petals
(Wagstaff et al., 2003) clearly shows that PCD is already occurring at relatively early stages
of petal senescence. In many flowers (e.g., Arabidopsis and tobacco), senescence, and thus
PCD is triggered by ethylene (Stead and van Doorn, 1994) and sometimes associated with
pollination (O'Neill and Nadau, 1997). However, in another group including lilies such as
Alstroemeria , the role of ethylene is less Clear. Calcium signaling and GTP-binding proteins
have been implicated in some species (Porat et al., 1994). Reactive oxygen species (ROS)
accumulation has also been reported both in ethylene-induced (Bartoli et al., 1996) and
ethylene-independent (Panavas and Rubinstein, 1998) petal senescence, together with a de-
crease in antioxidants (Bartoli et al., 1997). There is often evidence of tonoplast invagination
(Matile and Winkenbach, 1971; Phillips and Kende, 1980) or the formation of vesicles and in
the final stages only a thin layer of cytoplasm remains (Stead and van Doorn, 1994; Wagstaff
et al., 2003). Changes in membrane composition, fluidity, and peroxidation occur in several
species (Rubinstein, 2000). In some cases, such as carnation ( Dianthuscaryophyllus ; Fobel
et al., 1987), daylily ( Hemerocallis hybrid; Panavas and Rubinstein, 1998), and rose ( Rosa
hybrid; Fukuchi-Mizutani et al., 2000), lipid peroxidation (e.g., through the action of lipoxy-
genases (LOX) may be one of the key factors effecting loss of membrane integrity. However,
in other species like Alstroemeria (Leverentz et al., 2002), loss of membrane semiperme-
ability was chronologically separated from LOX activity that had declined by over 80% by
the onset of electrolyte leakage. However, loss of membrane function is the result of con-
certed activities of several enzymes and cannot be related to the function of a single enzyme
(Paliyath and Droillard, 1992; Chapter 9). DNA laddering has been found in some petals
such as Alstroemeria (Wagstaff et al., 2003) and gladiolus (Arora and Singh, 2006; Fig. 5.1)
and pea (Orzaez and Granell, 1997b), and both nucleases (Panavas et al. 1999; Breeze