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Learning to breathe : developmental phase transitions in oxygen status

(2017) TRENDS IN PLANT SCIENCE. 22(2). p.140-153
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Abstract
Plants are developmentally disposed to significant changes in oxygen availability, but our understanding of the importance of hypoxia is almost entirely limited to stress biology. Differential patterns of the abundance of oxygen, nitric oxide ((NO)-N-center dot), and reactive oxygen species (ROS), as well as of redox potential, occur in organs and meristems, and examples are emerging in the literature of mechanistic relationships of these to development. We describe here the convergence of these cues in meristematic and reproductive tissues, and discuss the evidence for regulated hypoxic niches within which oxygen-, ROS-, (NO)-N-center dot-, and redox-dependent signalling curate developmental transitions in plants.
Keywords
END RULE PATHWAY, ROOT QUIESCENT CENTER, STEM-CELL NICHE, NITRIC-OXIDE, REACTIVE OXYGEN, SEED-GERMINATION, MITOCHONDRIAL BIOGENESIS, ARABIDOPSIS, SHOOT, REDOX REGULATION, HEMOGLOBIN EXPRESSION

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Chicago
Considine, Michael J, Pedro Diaz-Vivancos, Pavel Kerchev, Santiago Signorelli, Patricia Agudelo-Romero, Daniel J Gibbs, and Christine H Foyer. 2017. “Learning to Breathe : Developmental Phase Transitions in Oxygen Status.” Trends in Plant Science 22 (2): 140–153.
APA
Considine, M. J., Diaz-Vivancos, P., Kerchev, P., Signorelli, S., Agudelo-Romero, P., Gibbs, D. J., & Foyer, C. H. (2017). Learning to breathe : developmental phase transitions in oxygen status. TRENDS IN PLANT SCIENCE, 22(2), 140–153.
Vancouver
1.
Considine MJ, Diaz-Vivancos P, Kerchev P, Signorelli S, Agudelo-Romero P, Gibbs DJ, et al. Learning to breathe : developmental phase transitions in oxygen status. TRENDS IN PLANT SCIENCE. 2017;22(2):140–53.
MLA
Considine, Michael J, Pedro Diaz-Vivancos, Pavel Kerchev, et al. “Learning to Breathe : Developmental Phase Transitions in Oxygen Status.” TRENDS IN PLANT SCIENCE 22.2 (2017): 140–153. Print.
@article{8516854,
  abstract     = {Plants are developmentally disposed to significant changes in oxygen availability, but our understanding of the importance of hypoxia is almost entirely limited to stress biology. Differential patterns of the abundance of oxygen, nitric oxide ((NO)-N-center dot), and reactive oxygen species (ROS), as well as of redox potential, occur in organs and meristems, and examples are emerging in the literature of mechanistic relationships of these to development. We describe here the convergence of these cues in meristematic and reproductive tissues, and discuss the evidence for regulated hypoxic niches within which oxygen-, ROS-, (NO)-N-center dot-, and redox-dependent signalling curate developmental transitions in plants.},
  author       = {Considine, Michael J and Diaz-Vivancos, Pedro and Kerchev, Pavel and Signorelli, Santiago and Agudelo-Romero, Patricia and Gibbs, Daniel J and Foyer, Christine H},
  issn         = {1360-1385},
  journal      = {TRENDS IN PLANT SCIENCE},
  keyword      = {END RULE PATHWAY,ROOT QUIESCENT CENTER,STEM-CELL NICHE,NITRIC-OXIDE,REACTIVE OXYGEN,SEED-GERMINATION,MITOCHONDRIAL BIOGENESIS,ARABIDOPSIS,SHOOT,REDOX REGULATION,HEMOGLOBIN EXPRESSION},
  language     = {eng},
  number       = {2},
  pages        = {140--153},
  title        = {Learning to breathe : developmental phase transitions in oxygen status},
  url          = {http://dx.doi.org/10.1016/j.tplants.2016.11.013},
  volume       = {22},
  year         = {2017},
}

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