Cargando…

Artificial Intelligence, DNA Mimicry, and Human Health

The molecular evolution of genomic DNA across diverse plant and animal phyla involved dynamic registrations of sequence modifications to maintain existential homeostasis to increasingly complex patterns of environmental stressors. As an essential corollary, driver effects of positive evolutionary pr...

Descripción completa

Detalles Bibliográficos
Autores principales: Stefano, George B., Kream, Richard M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566202/
https://www.ncbi.nlm.nih.gov/pubmed/28804119
http://dx.doi.org/10.12659/MSM.906498
_version_ 1783258507418533888
author Stefano, George B.
Kream, Richard M.
author_facet Stefano, George B.
Kream, Richard M.
author_sort Stefano, George B.
collection PubMed
description The molecular evolution of genomic DNA across diverse plant and animal phyla involved dynamic registrations of sequence modifications to maintain existential homeostasis to increasingly complex patterns of environmental stressors. As an essential corollary, driver effects of positive evolutionary pressure are hypothesized to effect concerted modifications of genomic DNA sequences to meet expanded platforms of regulatory controls for successful implementation of advanced physiological requirements. It is also clearly apparent that preservation of updated registries of advantageous modifications of genomic DNA sequences requires coordinate expansion of convergent cellular proofreading/error correction mechanisms that are encoded by reciprocally modified genomic DNA. Computational expansion of operationally defined DNA memory extends to coordinate modification of coding and previously under-emphasized noncoding regions that now appear to represent essential reservoirs of untapped genetic information amenable to evolutionary driven recruitment into the realm of biologically active domains. Additionally, expansion of DNA memory potential via chemical modification and activation of noncoding sequences is targeted to vertical augmentation and integration of an expanded cadre of transcriptional and epigenetic regulatory factors affecting linear coding of protein amino acid sequences within open reading frames. The burgeoning Artificial Intelligence (AI) discipline of biomolecular and DNA computing incorporates core operational machinery that includes input and output devices, memory, and biomolecular logic gates in order to utilize the potentially inexhaustible information technology (IT) capacity of genomic DNA [1]. Contextually, the dual application of DNA/RNA/protein complexed microcircuits to model AI deep learning and recurrent neural network paradigms carries the potential to significantly expand IT based strategies to effectively address a broad array of environmental challenges. Translational criteria to achieve effective augmentation of quality of life and life span require preemptive approaches to treat major disease states afflicting human populations from the perspective of personalized medicine that utilize reciprocally interactive genomic DNA databases [2,3]. To effectively advance these endeavors, the development of higher order AI-based bioinformatics based on complex cognitive processes linked to computational speed and accuracy may rely on evolutionary defined genomic DNA mimicry. The developmental elegance and critical biological importance of genomic DNA as a self-contained AI machine, crafted over the course of millions of years, establishes its primacy as the gold standard for design of higher order bioinformatics tools targeting human health processes. In summary, AI is not really artificial.
format Online
Article
Text
id pubmed-5566202
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher International Scientific Literature, Inc.
record_format MEDLINE/PubMed
spelling pubmed-55662022017-08-25 Artificial Intelligence, DNA Mimicry, and Human Health Stefano, George B. Kream, Richard M. Med Sci Monit Editorial The molecular evolution of genomic DNA across diverse plant and animal phyla involved dynamic registrations of sequence modifications to maintain existential homeostasis to increasingly complex patterns of environmental stressors. As an essential corollary, driver effects of positive evolutionary pressure are hypothesized to effect concerted modifications of genomic DNA sequences to meet expanded platforms of regulatory controls for successful implementation of advanced physiological requirements. It is also clearly apparent that preservation of updated registries of advantageous modifications of genomic DNA sequences requires coordinate expansion of convergent cellular proofreading/error correction mechanisms that are encoded by reciprocally modified genomic DNA. Computational expansion of operationally defined DNA memory extends to coordinate modification of coding and previously under-emphasized noncoding regions that now appear to represent essential reservoirs of untapped genetic information amenable to evolutionary driven recruitment into the realm of biologically active domains. Additionally, expansion of DNA memory potential via chemical modification and activation of noncoding sequences is targeted to vertical augmentation and integration of an expanded cadre of transcriptional and epigenetic regulatory factors affecting linear coding of protein amino acid sequences within open reading frames. The burgeoning Artificial Intelligence (AI) discipline of biomolecular and DNA computing incorporates core operational machinery that includes input and output devices, memory, and biomolecular logic gates in order to utilize the potentially inexhaustible information technology (IT) capacity of genomic DNA [1]. Contextually, the dual application of DNA/RNA/protein complexed microcircuits to model AI deep learning and recurrent neural network paradigms carries the potential to significantly expand IT based strategies to effectively address a broad array of environmental challenges. Translational criteria to achieve effective augmentation of quality of life and life span require preemptive approaches to treat major disease states afflicting human populations from the perspective of personalized medicine that utilize reciprocally interactive genomic DNA databases [2,3]. To effectively advance these endeavors, the development of higher order AI-based bioinformatics based on complex cognitive processes linked to computational speed and accuracy may rely on evolutionary defined genomic DNA mimicry. The developmental elegance and critical biological importance of genomic DNA as a self-contained AI machine, crafted over the course of millions of years, establishes its primacy as the gold standard for design of higher order bioinformatics tools targeting human health processes. In summary, AI is not really artificial. International Scientific Literature, Inc. 2017-08-14 /pmc/articles/PMC5566202/ /pubmed/28804119 http://dx.doi.org/10.12659/MSM.906498 Text en © Med Sci Monit, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Editorial
Stefano, George B.
Kream, Richard M.
Artificial Intelligence, DNA Mimicry, and Human Health
title Artificial Intelligence, DNA Mimicry, and Human Health
title_full Artificial Intelligence, DNA Mimicry, and Human Health
title_fullStr Artificial Intelligence, DNA Mimicry, and Human Health
title_full_unstemmed Artificial Intelligence, DNA Mimicry, and Human Health
title_short Artificial Intelligence, DNA Mimicry, and Human Health
title_sort artificial intelligence, dna mimicry, and human health
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566202/
https://www.ncbi.nlm.nih.gov/pubmed/28804119
http://dx.doi.org/10.12659/MSM.906498
work_keys_str_mv AT stefanogeorgeb artificialintelligencednamimicryandhumanhealth
AT kreamrichardm artificialintelligencednamimicryandhumanhealth