Abstract

The flower has a finite lifespan that is controlled largely by its role in sexual reproduction. Once the flower has been pollinated or is no longer receptive to pollination, the petals are programmed to senesce. A majority of the genes that are up-regulated during petal senescence, in both ethylene-sensitive and -insensitive flowers, encode proteins involved in the degradation of nucleic acids, proteins, lipids, fatty acids, and cell wall and membrane components. A smaller subset of these genes has a putative role in remobilizing nutrients, and only a few of these have been studied in detail. During senescence, carbohydrates (primarily sucrose) are transported from petals, and the degradation of macromolecules and organelles also allows the plant to salvage mineral nutrients from the petals before cell death. The remobilization of mineral nutrients from a few species has been investigated and will be reviewed in this article. Ethylene's role in nutrient remobilization is discussed by comparing nutrient changes during the senescence of ethylene-sensitive and -insensitive flowers, and by studies in transgenic petunias (Petunia × hybrida) that are insensitive to ethylene. Gene expression studies indicate that remobilization is a key feature of senescence, but some senescence-associated genes have different expression in leaves and petals. These gene expression patterns, along with differences in the nutrient content of leaves and petals, suggest that there are differences in the mechanisms of cellular degradation and nutrient transport in vegetative and floral organs. Autophagy may be the mechanism for large-scale degradation that allows for recycling during senescence, but it is unclear if this causes cell death. Future research should focus on autophagy and the regulation of ATG genes by ethylene during both leaf and petal senescence. We must identify the mechanisms by which individual mineral nutrients are transported out of senescing corollas in both ethylene-sensitive and -insensitive species.

Highlights

  • The purpose of the angiosperm flower is sexual reproduction, and some plants have colourful and/or fragrant flowers to aid in attracting pollinators

  • APG8e shows little change during leaf development and senescence, but is up-regulated during petal senescence (Wagstaff et al 2009). These findings suggest that differences in cellular constituents and nutrient content have led to the differences in autophagy that allow for the specific mechanisms of degradation and nutrient remobilization in senescing leaves and petals

  • This nutrient remobilization has been demonstrated in ethylenesensitive flowers and ethylene-insensitive flowers

Read more

Summary

Introduction

The purpose of the angiosperm flower is sexual reproduction, and some plants have colourful and/or fragrant flowers to aid in attracting pollinators. In pollinated petunias (detached flowers), N increases in the ovary were found to occur concomitantly with decreases in petal N content (Shibuya et al 2013), suggesting that the nutrients that are remobilized from pollinated senescing corollas are transported to the developing ovary. Ephemeral flower that opens and wilts within 1 day This very rapid senescence programme is accompanied by decreases in P, N, Cu, K, Zn and Mg, the exact same nutrients that are remobilized during the accelerated senescence of pollinated petunia corollas. APG8e shows little change during leaf development and senescence, but is up-regulated during petal senescence (Wagstaff et al 2009) These findings suggest that differences in cellular constituents and nutrient content have led to the differences in autophagy that allow for the specific mechanisms of degradation and nutrient remobilization in senescing leaves and petals. The petals may need to retain Fe during senescence to allow for ethylene production

Conclusions
Findings
Literature Cited
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call