ABSTRACT
The complex juvenile/maturity transition during a plant’s life cycle includes growth, reproduction, and senescence of its fundamental organs: leaves, flowers, and fruits. Growth and senescence of leaves, flowers, and fruits involve several genetic networks where the phytohormone ethylene plays a key role, together with other hormones, integrating different signals and allowing the onset of conditions favorable for stage progression, reproductive success and organ longevity. Changes in ethylene level, its perception, and the hormonal crosstalk directly or indirectly regulate the lifespan of plants. The present review focused on ethylene’s role in the development and senescence processes in leaves, flowers and fruits, paying special attention to the complex networks of ethylene crosstalk with other hormones. Moreover, aspects with limited information have been highlighted for future research, extending our understanding on the importance of ethylene during growth and senescence and boosting future research with the aim to improve the qualitative and quantitative traits of crops.
INTRODUCTION
The growth and development of plants under varied environmental conditions determine agricultural production. The growth, development, and senescence of plant’s organs can influence crop production by modulating photosynthesis, nutrient remobilization efficiency, and harvest index (Paltridge et al., 1984; Jing et al., 2005; Iqbal et al., 2012). Phytohormones have been shown to increase growth and yield of plants. The phytohormone ethylene controls growth and senescence of plants (Reid, 1995; Lutts et al., 1996; Thompson et al., 1998; Pierik et al., 2006; Masood et al., 2012; Nazar et al., 2014). Ethylene is regarded as a multifunctional phytohormone that regulates both growth, and senescence. It promotes or inhibits growth and senescence processes depending on its concentration, timing of application, and the plant species. The application of ethephon, an ethylene releasing compound enhanced ethylene evolution and increased leaf area of mustard at a lower concentration, while inhibited at higher concentration (Khan, 2005; Khan et al., 2008).
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