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Molecular epigenetics, chromatin, and NeuroAIDS/HIV: Immunopathological implications

Epigenetics studies factors related to the organism and environment that modulate inheritance from generation to generation. Molecular epigenetics examines non-coding DNA (ncdDNA) vs. coding DNA (cdDNA), and pertains to every domain of physiology, including immune and brain function. Molecular carto...

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Autores principales: Chiappelli, Francesco, Shapshak, Paul, Commins, Deborah, Singer, Elyse, Minagar, Alireza, Oluwadara, Oluwadayo, Prolo, Paolo, Pellionisz, Andras J
Formato: Texto
Lenguaje:English
Publicado: Biomedical Informatics Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586137/
https://www.ncbi.nlm.nih.gov/pubmed/19052666
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author Chiappelli, Francesco
Shapshak, Paul
Commins, Deborah
Singer, Elyse
Minagar, Alireza
Oluwadara, Oluwadayo
Prolo, Paolo
Pellionisz, Andras J
author_facet Chiappelli, Francesco
Shapshak, Paul
Commins, Deborah
Singer, Elyse
Minagar, Alireza
Oluwadara, Oluwadayo
Prolo, Paolo
Pellionisz, Andras J
author_sort Chiappelli, Francesco
collection PubMed
description Epigenetics studies factors related to the organism and environment that modulate inheritance from generation to generation. Molecular epigenetics examines non-coding DNA (ncdDNA) vs. coding DNA (cdDNA), and pertains to every domain of physiology, including immune and brain function. Molecular cartography, including genomics, proteomics, and interactomics, seeks to recognize and to identify the multi-faceted and intricate array of interacting genes and gene products that characterize the function and specialization of each individual cell in the context of cell-cell interaction, tissue, and organ function. Molecular cartography, epigenetics, and chromatin assembly, repair and remodeling (CARR), which, together with the RNA interfering signaling complex (RISC), is responsible for much of the control and regulation of gene expression, intersect. We describe current and ongoing studies aimed to apply these overlapping areas of research, CARR and RISC, to a novel understanding of the immuno-neuropathology of HIV-1 infection, as an example. Taken together, the arguments presented here lead to a novel working hypothesis of molecular immune epigenetics as it pertains to HIV/AIDS, and the immunopathology of HIV-1-infected CD4+ cells. Specifically, we discuss these views in the context of the structure-function relationship of chromatin, the cdDNA/ncdDNA ratio, and possible nucleotide divergence in the untranslated regions (UTRs) of mature mRNA intronic and intergenic DNA sequences, and putative catastrophic consequences for immune surveillance and the preservation of health in HIV/AIDS. Here, we discuss the immunopathology of HIV Infection, with emphasis on CARR in cellular, humoral and molecular immune epigenetics.
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spelling pubmed-25861372008-12-03 Molecular epigenetics, chromatin, and NeuroAIDS/HIV: Immunopathological implications Chiappelli, Francesco Shapshak, Paul Commins, Deborah Singer, Elyse Minagar, Alireza Oluwadara, Oluwadayo Prolo, Paolo Pellionisz, Andras J Bioinformation Current Trends Epigenetics studies factors related to the organism and environment that modulate inheritance from generation to generation. Molecular epigenetics examines non-coding DNA (ncdDNA) vs. coding DNA (cdDNA), and pertains to every domain of physiology, including immune and brain function. Molecular cartography, including genomics, proteomics, and interactomics, seeks to recognize and to identify the multi-faceted and intricate array of interacting genes and gene products that characterize the function and specialization of each individual cell in the context of cell-cell interaction, tissue, and organ function. Molecular cartography, epigenetics, and chromatin assembly, repair and remodeling (CARR), which, together with the RNA interfering signaling complex (RISC), is responsible for much of the control and regulation of gene expression, intersect. We describe current and ongoing studies aimed to apply these overlapping areas of research, CARR and RISC, to a novel understanding of the immuno-neuropathology of HIV-1 infection, as an example. Taken together, the arguments presented here lead to a novel working hypothesis of molecular immune epigenetics as it pertains to HIV/AIDS, and the immunopathology of HIV-1-infected CD4+ cells. Specifically, we discuss these views in the context of the structure-function relationship of chromatin, the cdDNA/ncdDNA ratio, and possible nucleotide divergence in the untranslated regions (UTRs) of mature mRNA intronic and intergenic DNA sequences, and putative catastrophic consequences for immune surveillance and the preservation of health in HIV/AIDS. Here, we discuss the immunopathology of HIV Infection, with emphasis on CARR in cellular, humoral and molecular immune epigenetics. Biomedical Informatics Publishing Group 2008-10-07 /pmc/articles/PMC2586137/ /pubmed/19052666 Text en © 2008 Biomedical Informatics Publishing Group This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited.
spellingShingle Current Trends
Chiappelli, Francesco
Shapshak, Paul
Commins, Deborah
Singer, Elyse
Minagar, Alireza
Oluwadara, Oluwadayo
Prolo, Paolo
Pellionisz, Andras J
Molecular epigenetics, chromatin, and NeuroAIDS/HIV: Immunopathological implications
title Molecular epigenetics, chromatin, and NeuroAIDS/HIV: Immunopathological implications
title_full Molecular epigenetics, chromatin, and NeuroAIDS/HIV: Immunopathological implications
title_fullStr Molecular epigenetics, chromatin, and NeuroAIDS/HIV: Immunopathological implications
title_full_unstemmed Molecular epigenetics, chromatin, and NeuroAIDS/HIV: Immunopathological implications
title_short Molecular epigenetics, chromatin, and NeuroAIDS/HIV: Immunopathological implications
title_sort molecular epigenetics, chromatin, and neuroaids/hiv: immunopathological implications
topic Current Trends
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586137/
https://www.ncbi.nlm.nih.gov/pubmed/19052666
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