Abstract
Ethylene is a gaseous phytohormone and the first of this hormone class to be discovered. It is the simplest olefin gas and is biosynthesized by plants to regulate plant development, growth, and stress responses via a well-studied signaling pathway. One of the earliest reported responses to ethylene is the triple response. This response is common in eudicot seedlings grown in the dark and is characterized by reduced growth of the root and hypocotyl, an exaggerated apical hook, and a thickening of the hypocotyl. This proved a useful assay for genetic screens and enabled the identification of many components of the ethylene-signaling pathway. These components include a family of ethylene receptors in the membrane of the endoplasmic reticulum (ER); a protein kinase, called constitutive triple response 1 (CTR1); an ER-localized transmembrane protein of unknown biochemical activity, called ethylene-insensitive 2 (EIN2); and transcription factors such as EIN3, EIN3-like (EIL), and ethylene response factors (ERFs). These studies led to a linear model, according to which in the absence of ethylene, its cognate receptors signal to CTR1, which inhibits EIN2 and prevents downstream signaling. Ethylene acts as an inverse agonist by inhibiting its receptors, resulting in lower CTR1 activity, which releases EIN2 inhibition. EIN2 alters transcription and translation, leading to most ethylene responses. Although this canonical pathway is the predominant signaling cascade, alternative pathways also affect ethylene responses. This review summarizes our current understanding of ethylene signaling, including these alternative pathways, and discusses how ethylene signaling has been manipulated for agricultural and horticultural applications.
Highlights
Ethylene is a gaseous phytohormone and the first of this hormone class to be discovered
The details about ethylene signal transduction provided in this review illustrate that we know many important aspects of how plants perceive ethylene
This includes a new appreciation that the ethylene receptors signal via alternative pathways, in addition to the canonical pathway that was originally delineated in genetic screens
Summary
There is recent evidence that ETR1 and ETR2 are signaling independently of CTR1 to cause the changes in ABA responsiveness, but the exact pathway has yet to be determined [84] These observations indicate that there are likely to be differences in the biochemical output between receptor isoforms. Mao huzi 3 (mhz3) mutants are ethylene-insensitive, and the MHZ3 protein physically interacts with OsEIN2-N and regulates OsEIN2 abundance; similar genes have been identified in Arabidopsis that affect ethylene signaling [131, 132]. These data indicate the need to further study EIN2-N to delineate the mechanism by which it affects ethylene signaling. There are still gaps in our understanding of this signal transduction pathway
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