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Deconvoluting lung evolution: from phenotypes to gene regulatory networks

Speakers in this symposium presented examples of respiratory regulation that broadly illustrate principles of evolution from whole organ to genes. The swim bladder and lungs of aquatic and terrestrial organisms arose independently from a common primordial “respiratory pharynx” but not from each othe...

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Autores principales: Torday, John S., Rehan, Virender K., Hicks, James W., Wang, Tobias, Maina, John, Weibel, Ewald R., Hsia, Connie C.W., Sommer, Ralf J., Perry, Steven F.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2895359/
https://www.ncbi.nlm.nih.gov/pubmed/20607138
http://dx.doi.org/10.1093/icb/icm069
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author Torday, John S.
Rehan, Virender K.
Hicks, James W.
Wang, Tobias
Maina, John
Weibel, Ewald R.
Hsia, Connie C.W.
Sommer, Ralf J.
Perry, Steven F.
author_facet Torday, John S.
Rehan, Virender K.
Hicks, James W.
Wang, Tobias
Maina, John
Weibel, Ewald R.
Hsia, Connie C.W.
Sommer, Ralf J.
Perry, Steven F.
author_sort Torday, John S.
collection PubMed
description Speakers in this symposium presented examples of respiratory regulation that broadly illustrate principles of evolution from whole organ to genes. The swim bladder and lungs of aquatic and terrestrial organisms arose independently from a common primordial “respiratory pharynx” but not from each other. Pathways of lung evolution are similar between crocodiles and birds but a low compliance of mammalian lung may have driven the development of the diaphragm to permit lung inflation during inspiration. To meet the high oxygen demands of flight, bird lungs have evolved separate gas exchange and pump components to achieve unidirectional ventilation and minimize dead space. The process of “screening” (removal of oxygen from inspired air prior to entering the terminal units) reduces effective alveolar oxygen tension and potentially explains why nonathletic large mammals possess greater pulmonary diffusing capacities than required by their oxygen consumption. The “primitive” central admixture of oxygenated and deoxygenated blood in the incompletely divided reptilian heart is actually co-regulated with other autonomic cardiopulmonary responses to provide flexible control of arterial oxygen tension independent of ventilation as well as a unique mechanism for adjusting metabolic rate. Some of the most ancient oxygen-sensing molecules, i.e., hypoxia-inducible factor-1alpha and erythropoietin, are up-regulated during mammalian lung development and growth under apparently normoxic conditions, suggesting functional evolution. Normal alveolarization requires pleiotropic growth factors acting via highly conserved cell–cell signal transduction, e.g., parathyroid hormone-related protein transducing at least partly through the Wingless/int pathway. The latter regulates morphogenesis from nematode to mammal. If there is commonality among these diverse respiratory processes, it is that all levels of organization, from molecular signaling to structure to function, co-evolve progressively, and optimize an existing gas-exchange framework.
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spelling pubmed-28953592010-07-02 Deconvoluting lung evolution: from phenotypes to gene regulatory networks Torday, John S. Rehan, Virender K. Hicks, James W. Wang, Tobias Maina, John Weibel, Ewald R. Hsia, Connie C.W. Sommer, Ralf J. Perry, Steven F. Integr Comp Biol Special Section on Respiratory Biology Speakers in this symposium presented examples of respiratory regulation that broadly illustrate principles of evolution from whole organ to genes. The swim bladder and lungs of aquatic and terrestrial organisms arose independently from a common primordial “respiratory pharynx” but not from each other. Pathways of lung evolution are similar between crocodiles and birds but a low compliance of mammalian lung may have driven the development of the diaphragm to permit lung inflation during inspiration. To meet the high oxygen demands of flight, bird lungs have evolved separate gas exchange and pump components to achieve unidirectional ventilation and minimize dead space. The process of “screening” (removal of oxygen from inspired air prior to entering the terminal units) reduces effective alveolar oxygen tension and potentially explains why nonathletic large mammals possess greater pulmonary diffusing capacities than required by their oxygen consumption. The “primitive” central admixture of oxygenated and deoxygenated blood in the incompletely divided reptilian heart is actually co-regulated with other autonomic cardiopulmonary responses to provide flexible control of arterial oxygen tension independent of ventilation as well as a unique mechanism for adjusting metabolic rate. Some of the most ancient oxygen-sensing molecules, i.e., hypoxia-inducible factor-1alpha and erythropoietin, are up-regulated during mammalian lung development and growth under apparently normoxic conditions, suggesting functional evolution. Normal alveolarization requires pleiotropic growth factors acting via highly conserved cell–cell signal transduction, e.g., parathyroid hormone-related protein transducing at least partly through the Wingless/int pathway. The latter regulates morphogenesis from nematode to mammal. If there is commonality among these diverse respiratory processes, it is that all levels of organization, from molecular signaling to structure to function, co-evolve progressively, and optimize an existing gas-exchange framework. Oxford University Press 2007-10 2007-07-26 /pmc/articles/PMC2895359/ /pubmed/20607138 http://dx.doi.org/10.1093/icb/icm069 Text en © 2007 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Section on Respiratory Biology
Torday, John S.
Rehan, Virender K.
Hicks, James W.
Wang, Tobias
Maina, John
Weibel, Ewald R.
Hsia, Connie C.W.
Sommer, Ralf J.
Perry, Steven F.
Deconvoluting lung evolution: from phenotypes to gene regulatory networks
title Deconvoluting lung evolution: from phenotypes to gene regulatory networks
title_full Deconvoluting lung evolution: from phenotypes to gene regulatory networks
title_fullStr Deconvoluting lung evolution: from phenotypes to gene regulatory networks
title_full_unstemmed Deconvoluting lung evolution: from phenotypes to gene regulatory networks
title_short Deconvoluting lung evolution: from phenotypes to gene regulatory networks
title_sort deconvoluting lung evolution: from phenotypes to gene regulatory networks
topic Special Section on Respiratory Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2895359/
https://www.ncbi.nlm.nih.gov/pubmed/20607138
http://dx.doi.org/10.1093/icb/icm069
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