Helen J Ougham | PubMed Health

PubMed2005

The colors of autumn leaves as symptoms of cellular recycling and defenses against environmental stresses.

The color changes that occur during foliar senescence are directly related to the regulation of nutrient mobilization and resorption from leaf cells, often under conditions of biotic and abiotic stress. Chlorophyll is degraded through a metabolic pathway that becomes specifically activated in senescence. Chlorophyll catabolic enzymes and genes have been identified and characterized and aspects of their regulation analyzed. Particular genetic interventions in the pathway lead to disruptions in protein mobilization and increased sensitivity to light-dependent cell damage and death. The chemistry and metabolism of carotenoid and anthocyanin pigments in senescing leaves are considered. Bright autumn colors observed in the foliage of some woody species have been hypothesized to act as a defense signal to potential insect herbivores. Critical consideration of the biochemical and physiological features of normal leaf senescence leads to the conclusion that accumulating or unmasking compounds with new colors are unlikely to represent a costly investment on the part of the tree. The influences of human evolutionary and social history on our own perception of autumn coloration are discussed. The possibility that insect herbivores may respond to volatiles emitted during leaf senescence, rather than to bright colors, is also presented. Finally, some new approaches to the analysis of protein recycling in senescence are briefly considered.

Animals↗

PubMed2003

Defining senescence and death.

This article evaluates features of leaf and flower senescence that are shared with, or are different from, those of other terminal events in plant development. Alterations of plastid structure and function in senescence are often reversible and it is argued that such changes represent a process of transdifferentiation or metaplasia rather than deterioration. It may be that the irreversible senescence of many flowers and some leaves represents the loss of ancestral plasticity during evolution. Reversibility serves to distinguish senescence fundamentally from programmed cell death (PCD), as does the fact that viability is essential for the initiation and progress of cell senescence. Senescence (particularly its timing and location) requires new gene transcription, but the syndrome is also subject to significant post- transcriptional and post-translational regulation. The reversibility of senescence must relate to the plastic, facultative nature of underlying molecular controls. Senescence appears to be cell-autonomous, though definitive evidence is required to substantiate this. The vacuole plays at least three key roles in the development of senescing cells: it defends the cell against biotic and abiotic damage, thus preserving viability, it accumulates metabolites with other functions, such as animal attractants, and it terminates senescence by becoming autolytic and facilitating true cell death. The mechanisms of PCD in plants bear a certain relation to those of apoptosis, and some processes, such as nucleic acid degradation, are superficially similar to aspects of the senescence syndrome. It is concluded that, in terms of physiological components and their controls, senescence and PCD are at best only distantly related.

Apoptosis↗