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Non-Random Genome Editing and Natural Cellular Engineering in Cognition-Based Evolution

Neo-Darwinism presumes that biological variation is a product of random genetic replication errors and natural selection. Cognition-Based Evolution (CBE) asserts a comprehensive alternative approach to phenotypic variation and the generation of biological novelty. In CBE, evolutionary variation is t...

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Autores principales: Miller, William B., Enguita, Francisco J., Leitão, Ana Lúcia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148535/
https://www.ncbi.nlm.nih.gov/pubmed/34066959
http://dx.doi.org/10.3390/cells10051125
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author Miller, William B.
Enguita, Francisco J.
Leitão, Ana Lúcia
author_facet Miller, William B.
Enguita, Francisco J.
Leitão, Ana Lúcia
author_sort Miller, William B.
collection PubMed
description Neo-Darwinism presumes that biological variation is a product of random genetic replication errors and natural selection. Cognition-Based Evolution (CBE) asserts a comprehensive alternative approach to phenotypic variation and the generation of biological novelty. In CBE, evolutionary variation is the product of natural cellular engineering that permits purposive genetic adjustments as cellular problem-solving. CBE upholds that the cornerstone of biology is the intelligent measuring cell. Since all biological information that is available to cells is ambiguous, multicellularity arises from the cellular requirement to maximize the validity of available environmental information. This is best accomplished through collective measurement purposed towards maintaining and optimizing individual cellular states of homeorhesis as dynamic flux that sustains cellular equipoise. The collective action of the multicellular measurement and assessment of information and its collaborative communication is natural cellular engineering. Its yield is linked cellular ecologies and mutualized niche constructions that comprise biofilms and holobionts. In this context, biological variation is the product of collective differential assessment of ambiguous environmental cues by networking intelligent cells. Such concerted action is enabled by non-random natural genomic editing in response to epigenetic impacts and environmental stresses. Random genetic activity can be either constrained or deployed as a ‘harnessing of stochasticity’. Therefore, genes are cellular tools. Selection filters cellular solutions to environmental stresses to assure continuous cellular-organismal-environmental complementarity. Since all multicellular eukaryotes are holobionts as vast assemblages of participants of each of the three cellular domains (Prokaryota, Archaea, Eukaryota) and the virome, multicellular variation is necessarily a product of co-engineering among them.
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spelling pubmed-81485352021-05-26 Non-Random Genome Editing and Natural Cellular Engineering in Cognition-Based Evolution Miller, William B. Enguita, Francisco J. Leitão, Ana Lúcia Cells Review Neo-Darwinism presumes that biological variation is a product of random genetic replication errors and natural selection. Cognition-Based Evolution (CBE) asserts a comprehensive alternative approach to phenotypic variation and the generation of biological novelty. In CBE, evolutionary variation is the product of natural cellular engineering that permits purposive genetic adjustments as cellular problem-solving. CBE upholds that the cornerstone of biology is the intelligent measuring cell. Since all biological information that is available to cells is ambiguous, multicellularity arises from the cellular requirement to maximize the validity of available environmental information. This is best accomplished through collective measurement purposed towards maintaining and optimizing individual cellular states of homeorhesis as dynamic flux that sustains cellular equipoise. The collective action of the multicellular measurement and assessment of information and its collaborative communication is natural cellular engineering. Its yield is linked cellular ecologies and mutualized niche constructions that comprise biofilms and holobionts. In this context, biological variation is the product of collective differential assessment of ambiguous environmental cues by networking intelligent cells. Such concerted action is enabled by non-random natural genomic editing in response to epigenetic impacts and environmental stresses. Random genetic activity can be either constrained or deployed as a ‘harnessing of stochasticity’. Therefore, genes are cellular tools. Selection filters cellular solutions to environmental stresses to assure continuous cellular-organismal-environmental complementarity. Since all multicellular eukaryotes are holobionts as vast assemblages of participants of each of the three cellular domains (Prokaryota, Archaea, Eukaryota) and the virome, multicellular variation is necessarily a product of co-engineering among them. MDPI 2021-05-07 /pmc/articles/PMC8148535/ /pubmed/34066959 http://dx.doi.org/10.3390/cells10051125 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Miller, William B.
Enguita, Francisco J.
Leitão, Ana Lúcia
Non-Random Genome Editing and Natural Cellular Engineering in Cognition-Based Evolution
title Non-Random Genome Editing and Natural Cellular Engineering in Cognition-Based Evolution
title_full Non-Random Genome Editing and Natural Cellular Engineering in Cognition-Based Evolution
title_fullStr Non-Random Genome Editing and Natural Cellular Engineering in Cognition-Based Evolution
title_full_unstemmed Non-Random Genome Editing and Natural Cellular Engineering in Cognition-Based Evolution
title_short Non-Random Genome Editing and Natural Cellular Engineering in Cognition-Based Evolution
title_sort non-random genome editing and natural cellular engineering in cognition-based evolution
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148535/
https://www.ncbi.nlm.nih.gov/pubmed/34066959
http://dx.doi.org/10.3390/cells10051125
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