Faculty Opinions recommendation of Nighttime sugar starvation orchestrates gibberellin biosynthesis and plant growth in Arabidopsis.

Author(s):  
Sjef Smeekens ◽  
Johannes Hanson
2013 ◽  
Vol 25 (10) ◽  
pp. 3760-3769 ◽  
Author(s):  
Eleonora Paparelli ◽  
Sandro Parlanti ◽  
Silvia Gonzali ◽  
Giacomo Novi ◽  
Lorenzo Mariotti ◽  
...  

2019 ◽  
Vol 116 (43) ◽  
pp. 21925-21935 ◽  
Author(s):  
Yi-Shih Chen ◽  
Tuan-Hua David Ho ◽  
Lihong Liu ◽  
Ding Hua Lee ◽  
Chun-Hua Lee ◽  
...  

Autotrophic plants have evolved distinctive mechanisms for maintaining a range of homeostatic states for sugars. The on/off switch of reversible gene expression by sugar starvation/provision represents one of the major mechanisms by which sugar levels are maintained, but the details remain unclear. α-Amylase (αAmy) is the key enzyme for hydrolyzing starch into sugars for plant growth, and it is induced by sugar starvation and repressed by sugar provision. αAmy can also be induced by various other stresses, but the physiological significance is unclear. Here, we reveal that the on/off switch of αAmy expression is regulated by 2 MYB transcription factors competing for the same promoter element. MYBS1 promotes αAmy expression under sugar starvation, whereas MYBS2 represses it. Sugar starvation promotes nuclear import of MYBS1 and nuclear export of MYBS2, whereas sugar provision has the opposite effects. Phosphorylation of MYBS2 at distinct serine residues plays important roles in regulating its sugar-dependent nucleocytoplasmic shuttling and maintenance in cytoplasm by 14-3-3 proteins. Moreover, dehydration, heat, and osmotic stress repress MYBS2 expression, thereby inducing αAmy3. Importantly, activation of αAmy3 and suppression of MYBS2 enhances plant growth, stress tolerance, and total grain weight per plant in rice. Our findings reveal insights into a unique regulatory mechanism for an on/off switch of reversible gene expression in maintaining sugar homeostatic states, which tightly regulates plant growth and development, and also highlight MYBS2 and αAmy3 as potential targets for crop improvement.


2017 ◽  
Vol 41 (2) ◽  
pp. 65-71 ◽  
Author(s):  
James R. Hanson

The scope of the microbiological transformation of ent-kaurenoid diterpenes by the fungus Fusarium (Gibberella) fujikuroi which utilise the ent-kaurene and ent-kauren-19-oic acid oxidases and the ring contraction of ring B to gibberellin is reviewed. Constraints arising from the presence of 3α, 15α and 18-hydroxyl groups are noted. The development of a group of potential plant growth regulators which inhibit the ring contraction step in gibberellin biosynthesis is described.


2020 ◽  
Author(s):  
Putri Prasetyaningrum ◽  
Lorenzo Mariotti ◽  
Maria Cristina Valeri ◽  
Giacomo Novi ◽  
Stijn Dhondt ◽  
...  

AbstractOptimal plant growth performance requires that the action of growth signals, such as gibberellins (GA), are coordinated with the availability of photo-assimilates. Here, we studied the links between gibberellin biosynthesis and carbon availability, and the subsequent effects on growth. The results presented here show that carbon availability, light and dark cues, and the clock ensure the timing and magnitude of gibberellin biosynthesis and that disruption of these mechanisms results in reduced gibberellin levels and expression of downstream genes. Carbon dependent nighttime induction of GIBBERELLIN 3-BETA-DIOXYGENASE 1 (GA3ox1) was severely hampered when preceded by a day of lowered light availability, leading specifically to reduced bioactive GA4 levels, and coinciding with a decline in leaf expansion rate during the night. We attribute this decline in leaf expansion mostly to reduced photo-assimilates. However, plants where gibberellin limitation was alleviated had significantly improved expansion demonstrating the relevance of gibberellins in growth control under varying carbon availability. Carbon dependent expression of upstream gibberellin biosynthesis genes (KAURENE SYNTHASE, KS and GIBBERELLIN 20 OXIDASE 1, GA20ox1) was not translated into metabolite changes within this short timeframe. We propose a model where the extent of nighttime biosynthesis of bioactive GA4 by GA3ox1 is determined by starch, as the nighttime carbon source, and so provides day-to-day adjustment of gibberellin responses.


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