Pleiotropy as the Mechanism for Evolving Novelty: Same Signal, Different Result

In contrast to the probabilistic way of thinking about pleiotropy as the random expression of a single gene that generates two or more distinct phenotypic traits, it is actually a deterministic consequence of the evolution of complex physiology from the unicellular state. Pleiotropic novelties emerg...

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Main Author: John S. Torday
Format: Article
Language:English
Published: MDPI AG 2015-06-01
Series:Biology
Subjects:
Online Access:http://www.mdpi.com/2079-7737/4/2/443
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spelling doaj-80bced9f7b7b41789783ebc201b58a8c2020-11-25T00:48:03ZengMDPI AGBiology2079-77372015-06-014244345910.3390/biology4020443biology4020443Pleiotropy as the Mechanism for Evolving Novelty: Same Signal, Different ResultJohn S. Torday0Harbor-UCLA Medical Center, 1124 West Carson Street, Torrance, CA 90502-2006, USAIn contrast to the probabilistic way of thinking about pleiotropy as the random expression of a single gene that generates two or more distinct phenotypic traits, it is actually a deterministic consequence of the evolution of complex physiology from the unicellular state. Pleiotropic novelties emerge through recombinations and permutations of cell-cell signaling exercised during reproduction based on both past and present physical and physiologic conditions, in service to the future needs of the organism for its continued survival. Functional homologies ranging from the lung to the kidney, skin, brain, thyroid and pituitary exemplify the evolutionary mechanistic strategy of pleiotropy. The power of this perspective is exemplified by the resolution of evolutionary gradualism and punctuated equilibrium in much the same way that Niels Bohr resolved the paradoxical duality of light as Complementarity.http://www.mdpi.com/2079-7737/4/2/443pleiotropygrowth factorgrowth factor receptorcell-cell interactionparathyroid hormone-related proteinprostaglandin E2β-adrendergic receptortype IV collagenadipocyte differentiation related proteinneutral lipid trafficking
collection DOAJ
language English
format Article
sources DOAJ
author John S. Torday
spellingShingle John S. Torday
Pleiotropy as the Mechanism for Evolving Novelty: Same Signal, Different Result
Biology
pleiotropy
growth factor
growth factor receptor
cell-cell interaction
parathyroid hormone-related protein
prostaglandin E2
β-adrendergic receptor
type IV collagen
adipocyte differentiation related protein
neutral lipid trafficking
author_facet John S. Torday
author_sort John S. Torday
title Pleiotropy as the Mechanism for Evolving Novelty: Same Signal, Different Result
title_short Pleiotropy as the Mechanism for Evolving Novelty: Same Signal, Different Result
title_full Pleiotropy as the Mechanism for Evolving Novelty: Same Signal, Different Result
title_fullStr Pleiotropy as the Mechanism for Evolving Novelty: Same Signal, Different Result
title_full_unstemmed Pleiotropy as the Mechanism for Evolving Novelty: Same Signal, Different Result
title_sort pleiotropy as the mechanism for evolving novelty: same signal, different result
publisher MDPI AG
series Biology
issn 2079-7737
publishDate 2015-06-01
description In contrast to the probabilistic way of thinking about pleiotropy as the random expression of a single gene that generates two or more distinct phenotypic traits, it is actually a deterministic consequence of the evolution of complex physiology from the unicellular state. Pleiotropic novelties emerge through recombinations and permutations of cell-cell signaling exercised during reproduction based on both past and present physical and physiologic conditions, in service to the future needs of the organism for its continued survival. Functional homologies ranging from the lung to the kidney, skin, brain, thyroid and pituitary exemplify the evolutionary mechanistic strategy of pleiotropy. The power of this perspective is exemplified by the resolution of evolutionary gradualism and punctuated equilibrium in much the same way that Niels Bohr resolved the paradoxical duality of light as Complementarity.
topic pleiotropy
growth factor
growth factor receptor
cell-cell interaction
parathyroid hormone-related protein
prostaglandin E2
β-adrendergic receptor
type IV collagen
adipocyte differentiation related protein
neutral lipid trafficking
url http://www.mdpi.com/2079-7737/4/2/443
work_keys_str_mv AT johnstorday pleiotropyasthemechanismforevolvingnoveltysamesignaldifferentresult
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